System and method for extracorporeal blood treatment

Abstract

To provide an extracorporeal blood treatment system for treating a subject suffering from cancer.SOLUTION: An extracorporeal blood treatment system (50) has a system computing unit (64). The system computing unit is adapted for receiving desired blood concentration GLNb of glutamine, receiving desired blood concentration GLUCOSEb of glucose, and receiving desired blood concentration of a ketone body KETONEb. The system computing unit is adapted for controlling a blood pump and a dialysate fluid pump so that the actual concentration value GLNa of glutamine is GLNb, the actual concentration value GLUCOSEa of glucose is Db, and the actual concentration value of ketone body is KETONEa.SELECTED DRAWING: Figure 2

Description

[Technical field]

[0001] The disclosure herein relates to extracorporeal blood therapy. More specifically, the disclosure relates to the use of extracorporeal blood therapy, such as hemodialysis, in the treatment of cancer, and systems for such therapy, as well as user interfaces for controlling and displaying data recorded during such extracorporeal blood therapy (sg historical data). [Background technology]

[0002] Most human cancer cells exhibit alterations in energy metabolism that distinguish them from normal cells. Normal cells obtain most of their energy through mitochondrial oxidative phosphorylation, an aerobic process in which glucose is oxidized to produce adenosine triphosphate, first by glycolysis and subsequently by the tricarboxylic acid (TCA) cycle. In contrast, this pathway is only secondary in cancer cells. This was first observed by Warburg in the 1920s. He noted that cancer cells metabolize glucose by glycolysis, followed by the production of lactate from pulvate. In normal cells, this occurs only under anaerobic conditions, but in cancer cells, this alternative pathway increases even in the presence of abundant oxygen. This phenomenon was named "aerobic glycolysis" or the "Warburg effect" (Warburg et al., 1927, Gen Physiol 8:519-530). The presence of a characteristic glycolytic phenotype in cancer cells was confirmed by subsequent studies, in which overexpression of enzymes involved in glycolysis was also observed in most cancer cells.

[0003] The metabolic transformations described above confer selective growth advantages to cancer cells and contribute to their ability to resist hypoxia and apoptosis. Many tumors grow in hypoxic environments because the rate of tumor cell proliferation exceeds the rate of new blood vessel formation. There are various metabolic alterations in cancer cells, but the most common and best known is their propensity to generate energy by aerobic glycolysis. In addition, many intermediates of glycolysis, such as ribose, glycerol, and serine, are also intermediates of biosynthetic and anabolic pathways essential during the growth and proliferation of cancer cells. Glycolysis also generates ATP from ADP, which allows for the maintenance and growth of cells in tumors. However, glycolysis is much less efficient than oxidative phosphorylation, so large amounts of glucose are required to generate sufficient amounts of ATP. Therefore, large amounts of glucose are required for this metabolic pathway. Many cancer cells become dependent on glucose as their primary energy source. For multiple reasons, glycolytic tumor cells are vulnerable when their glucose supply is targeted.

[0004] Furthermore, many cancer cells also exhibit glutamine toxicity: the high rate of glutamine uptake exhibited by glutamine-dependent cells is not only a consequence of its role as a nitrogen source in nucleotide and amino acid biosynthesis, but glutamine is also the major mitochondrial substrate in cancer, required to generate NADPH for redox regulation and macromolecular synthesis.

[0005] There are other metabolic changes in cancer that play important roles in survival, and importantly, many cancers show a remarkable ability to change their metabolic profile. This adaptability to withstand environmental challenges such as reduced glucose, glutamine, or oxygen is critical for cancer cell survival.

[0006] Furthermore, many cancer cells also exhibit a dependency on glutamine: not only is the high rate of glutamine uptake by glutamine-dependent cancer cells a consequence of its role as a nitrogen source for nucleotide and amino acid biosynthesis, but glutamine is also the major mitochondrial substrate in many cancers, required to generate NADPH for redox regulation and macromolecular synthesis.

[0007] Many metabolic changes exist in cancer, and various amino acids such as glutamine play key roles in cancer metabolism, controlling redox balance and generating building blocks for continued proliferation, and many cancers show a remarkable ability to utilize their alternative pathways and change their metabolic profile when they need to adapt to new metabolic limitations. This quality is a key feature for cancers and their ability to withstand environmental challenges when metabolic energy sources such as glucose, glutamine, and oxygen are scarce.

[0008] Therefore, to effectively impact cancer through metabolic approaches, it is important to affect metabolic systems from multiple directions: reduced glucose can be easily processed by most cancer cells, but when several metabolic possibilities are affected simultaneously (e.g. reduced glucose and glutamine), the sum of these changes becomes much more devastating than the individual parts.

[0009] In addition to glucose, ketones, and glutamine, which are the global energy sources for many cancers, serine and glycine fulfill important specific needs to sustain cancer cell growth and proliferation, for example through one-carbon metabolism. In addition to needing large amounts of energy, cancer cells also need to accumulate building blocks for building new cellular components, including nucleic acids, proteins, and lipids, as well as equally important cofactors for maintaining the cellular redox state (Amelio et al.: Trends. Biochem. Sci. (2014), Vol. 39 (4): 191-198)).

[0010] Studies have demonstrated that arginine is necessary for cell growth and can be limiting in conditions of rapid growth, and also affects survival when deprived of cancer cells (Albaugh et al., J. Surg. Oncol. (2017), Vol. 115(3), 273-280).

[0011] In view of the above, it has been suggested that lowering blood glucose levels may serve as a strategy to target a wide range of glycolysis-dependent tumors. Under hypoglycemic conditions, fats, especially ketone bodies, can replace glucose as the primary metabolic fuel in normal cells. However, many tumors have defects in the genes and enzymes required to metabolize lipids and ketone bodies for energy. Thus, a shift from carbohydrates to ketones for energy would specifically target the energy metabolism of glycolysis-dependent tumor cells (Seyfried et al, 2010, Nutrition and Metabolism, 7:7).

[0012] Following this approach, for example, WO 2011 / 070527 discloses a method for treating cancerous or non-cancerous proliferative diseases in an individual in which a hemodialysis machine is used to reduce blood glucose concentrations.

[0013] The use of a hemodialysis machine to lower blood glucose has the advantage that it can lower the glucose concentration in the blood, and thereby in a more controlled and effective manner, compared to glucose removal by diet. However, the method and device disclosed in WO 2011 / 070527 require blood glucose and blood glutamine sensors connected to the blood inlet flow, blood return flow and dialysate, all of which are connected to a central control unit of the hemodialysis machine. Furthermore, the central control unit of WO 2011 / 070527 is also connected to an electroencephalograph (EEG), which provides the central unit with information about spontaneous brain electrical activity that initiates the rise in glucose and glutamine levels. Such a large number of sensors and equipment leads to a high degree of complexity and associated high costs. Furthermore, patients undergoing this treatment must consume only a glucose-restricted diet for several days before embarking on the treatment. This is not an insignificant burden for the patient.

[0014] There is a constant need for improved methods for treating cancer. Summary of the Invention

[0015] In a first aspect of the present invention, there is provided an extracorporeal blood treatment system (50) for treating a subject suffering from cancer, said system comprising: Extracorporeal blood circuit (52a, 52b); Dialysate fluid circuit (54a, 54b); said extracorporeal blood circuit (52a, 52b) and dialysate fluid circuit (54a, 54b) separated by a membrane (59) of a filtration unit (58); at least one blood pump (60) for controlling the flow of blood through said blood circuits (52a, 52b); at least one dialysate fluid pump (62, 68) for controlling the flow of dialysate through said dialysate fluid circuit (54a, 54b); optionally, one or more infusion lines (66, 80, 81, 82), each infusion line adapted to be connected to said extracorporeal blood circuit (52a, 52b) or directly to the vascular system of the subject to be treated, each infusion line including an infusion pump; a system computing unit (64) operably connected to said blood pump (60) and said dialysate fluid pumps (62, 68) and optionally to one or more infusion pumps of said one or more infusion lines (66, 80, 81, 82), said system computing unit including a user interface including input means and display means; Including, The system computing unit (64) determines a desired blood concentration value of glutamine within the range of 0.1 to 0.5 mM GLN b adapted to receive (901); The system computing unit (64) determines a desired blood concentration value of glucose within the range of 2 to 4 mM. b adapted to receive (903) The system computing unit (64) receives a desired blood concentration value of ketone bodies, such as acetoacetate, β-hydroxybutyrate, or pharma- ceutically acceptable derivatives, esters, and salts thereof, in the range of 1 to 15 mM. b adapted to receive (905); The system computing unit (64) receives a concentration value GLN representing the concentration of glutamine or a pharma- ceutically acceptable glutamine-containing compound in the new dialysate fluid. P adapted to receive (902) The system computing unit (64) receives a concentration value GLUCOSE representative of the concentration of glucose in the new dialysate fluid. p adapted to receive (904); Optionally, the system computing unit (64) may generate a concentration value KETONE representing the concentration of ketone bodies, such as acetoacetate, β-hydroxybutyrate, or pharma- ceutically acceptable derivatives, esters, and salts thereof, in the fresh dialysate fluid. p adapted to receive (907); Optionally, the system computing unit (64) may also generate a concentration value KETONE representing the concentration of ketone bodies, such as acetoacetate, beta-hydroxybutyrate or pharma- ceutically acceptable derivatives, esters and salts thereof, in an infusion fluid infused into the extracorporeal blood line (52b) or directly into the vascular system of the subject to be treated via one of the one or more infusion lines (66, 80, 81, 82). i adapted to receive (906); The system computing unit (64) receives the actual concentration value of glutamine in the blood from the treated subject, GLN a and receiving (909) an actual blood concentration value of glucose in blood from the treated subject. a (910) and the actual concentration values ​​of ketone bodies such as acetoacetate and β-hydroxybutyrate KETONE a adapted to receive (911) The system computing unit (64) calculates the actual blood concentration value GLN of glutamine. a GLN b (912) below, and said actual blood concentration value GLUCOSE a GLUCOSE b adapted to control the blood pump (60) and the dialysate fluid pumps (62, 68) as described below (914); When the system (50) comprises one or more of the infusion lines (66, 80, 81, 82), and when one of the infusion lines (66, 80, 81, 82) is adapted to infuse the infusion solution into the extracorporeal vascular line (52b) or directly into the vascular system of the subject being treated, the system computing unit (64) is adapted to calculate the actual blood concentration value KETONE a KETONE b adapted to control (920) the infusion pump of the infusion line to Or, alternatively, If the system (50) does not include such infusion lines (66, 80, 81, 82), the system computing unit (64) a and KETONE b Compared with KETONE a <KETONE b if so, a message is displayed on the display informing the treated subject that he or she needs to consume an additional amount of ketone bodies or medium chain triglycerides.

[0016] In the present disclosure, the term "subject" relates to a human or animal patient in need of treatment.

[0017] In a preferred embodiment, the extracorporeal blood treatment system (50) comprises one or more of the infusion lines (66, 80, 81, 82), and the system computing unit (64) is adapted to receive (906) a concentration value KETONE representative of the concentration of ketone bodies, such as acetoacetate, beta-hydroxybutyrate, or pharma- ceutically acceptable derivatives, esters and salts thereof, in an infusion solution infused via one of the one or more infusion lines (66, 80, 81, 82) into the extracorporeal blood line (52b) or directly into the vascular system of the treated subject; and The system computing unit (64) calculates the actual blood concentration value KETONE a KETONEb (920) is adapted to control the infusion pump of the infusion line.

[0018] In a preferred embodiment, the system computing unit (64) is a and GLUCOSE a and actuating an associated infusion pump in one of said one or more infusion lines (66, 80, 81, 82), thereby a GLN b If the serum glutamine concentration is less than 100 mg / kg, start an infusion of a composition containing glutamine or a pharma- ceutically acceptable glutamine-containing compound (916) and / or administer the GLUCOSE a GLUCOSE b is adapted to initiate an infusion of a composition containing glucose if the GLN a GLN b is equal to GLUCOSE a GLUCOSE b The infusion is maintained until the infusion equals

[0019] The term "pharmaceutical acceptable glutamine-containing compound" refers to an oligopeptide, typically a dipeptide, in which at least one of the amino acid residues is glutamine. Typical examples of such dipeptides are L-alanyl-L-glutamine and L-glycyl-L-glutamine. Glutamine-containing compounds are typically used in place of glutamine in liquid compositions to enhance stability and solubility.

[0020] The term "ketone bodies" relates to water-soluble molecules containing a ketone group that can be produced by the liver from fatty acids. Typically, ketone bodies according to the invention are β-hydroxybutyric acid or its enantiomers (R)-β-hydroxybutyric acid, (S)-β-hydroxybutyric acid, or their pharma- ceutically acceptable derivatives, such as mixtures of enantiomers, or their pharma- ceutically acceptable salts, or their pharma-ceutically acceptable esters, as well as acetoacetates. Medium chain triglycerides are also considered to be derivatives of ketone bodies according to the invention. The term "medium chain triglycerides" or "MCT oil" refers to triglycerides with two or three fatty acids with an aliphatic tail of 6 to 12 carbon atoms. Such medium chain triglycerides or MCT oils may be converted into ketone bodies in the human body. Examples of infusion solutions containing ketone bodies or ketone body derivatives are Lipofundin® MCT / LCT 20% (B. Braun) or SMOFlipid® 20% (Fresenius Kabi). Further examples are described in WO 2018 / 114309. Since other ketone body derivatives are converted to either of these compounds in the subject's body, the actual ketone body concentration KETONE a As such, only concentrations of β-hydroxybutyrate and / or acetoacetate are detected in the subject's blood.

[0021] Preferably, the filtration membrane has a molecular weight cut-off (MWCO) of less than 60 kDa. More preferably, the filtration membrane has a MWCO of less than about 50 kDa or less than about 40 kDa (such as less than 30 kDa, less than 10 kDa, less than 5 kDa, or less than 2 kDa).

[0022] Preferably, the blood circuit comprises a thermal management system for heating or cooling blood in the blood line during use.

[0023] More preferably, the thermal management system is controllable to regulate the temperature of the blood in the blood circuit to a temperature between 20°C and 43°C.

[0024] Preferably, the system (50) further comprises one or more sensors (S, 90, 91, 92, 93) for detecting an analyte selected from the group of glucose, glutamine, and ketone bodies, the sensors (S, 90, 91, 92, 93) being preferably disposed in the outlet portion (54a) of the dialysate fluid circuit, the sensors being in communication with the system processing unit (64) and providing an output indicative of the concentration of the analyte in the blood, or preferably in the spent dialysate fluid, the system processing unit (64) being configured to determine a representative blood concentration of the analyte from the output of the sensors (S, 90, 91, 92, 93), thereby detecting a representative blood concentration of at least one, and preferably all, of the GLN. a , GLUCOSE a , and KETONE a Monitor.

[0025] In a second aspect, the present invention relates to a treatment set for use in an extracorporeal blood treatment system (50) according to the first aspect, said set comprising a filtration unit (58) having a membrane (59) dividing integrated blood lines (52a, 52b) and integrated dialysate fluid lines (54a, 54b), said blood lines (52a, 52b) and / or said dialysate fluid lines (54a, 54b) being resistant to GLN a , GLUCOSE a , and KETONE a The present invention provides a treatment set including a sensor (S, 90, 91, 92, 93) for monitoring at least one of the following:

[0026] As described below, suitable sensors and assays for analyzing glutamine, glucose, and ketone bodies are known in the art.

[0027] In a third aspect, the present invention provides a method of treating a subject suffering from cancer using a system (50), said system (50) comprising: Extracorporeal blood circuit (52a, 52b); Dialysate fluid circuit (54a, 54b); said extracorporeal blood circuit (52a, 52b) and dialysate fluid circuit (54a, 54b) separated by a membrane (59) of a filtration unit (58); at least one blood pump (60) for controlling the flow of blood through said blood circuits (52a, 52b); at least one dialysate fluid pump (62, 68) for controlling the flow of dialysate fluid through said dialysate fluid circuit (54a, 54b); and optionally, one or more infusion lines (66, 80, 81, 82), each infusion line adapted to be connected to the extracorporeal circuit (52a, 52b) or directly to the vascular system of the subject to be treated, each infusion line including an infusion pump; The method comprises: A concentration value GLN representing a desired blood concentration of glutamine in the range of 0.1 to 0.5 mM. b receiving (901); A concentration value GLUCOSE representing a desired blood concentration of glucose in the range of 2 to 4 mM. b receiving (903); A concentration value KETONE representing a desired blood concentration of a ketone body, such as acetoacetate, β-hydroxybutyrate, or pharma- ceutically acceptable salts, derivatives, and esters thereof, in the range of 1 to 15 mM. b receiving (905); A concentration value representing the concentration of glutamine or a pharma- tically acceptable glutamine-containing compound in the new dialysate fluid, GLN p receiving (902); A concentration value GLUCOSE representing the concentration of glucose in the dialysate fluid. p receiving (904); Optionally, said system computing unit; Optionally, a concentration value KETONE representing the concentration of ketone bodies, such as acetoacetate, β-hydroxybutyrate, or pharma- ceutically acceptable derivatives, esters, and salts thereof, in the new dialysate fluid. p receiving (907); Optionally, a concentration value KETONE representing the concentration of ketone bodies, such as acetoacetate, beta-hydroxybutyrate, or pharma- ceutically acceptable salts, derivatives, and esters thereof, in an infusion solution infused into the extracorporeal blood line (52b) or directly into the vascular system of the subject to be treated via one of the one or more infusion lines (66, 80, 81, 82). i receiving (906); a concentration value GLN representing the actual concentration of glutamine in the blood of the treated subject; a receiving (909); A concentration value GLUCOSE representing the actual glucose concentration in the blood of the treated subject. a receiving (910); a concentration value KETONE representing the actual concentration of ketone bodies, such as acetoacetate and β-hydroxybutyrate, in the blood of the treated subject; a receiving (911); The blood pump (60) and the at least one dialysate fluid pump (62, 68) are controlled to obtain the actual concentration value GLN a GLN b and the actual concentration value GLUCOSE a GLUCOSE b To be made (914) below; and When the system (50) comprises one or more of the infusion lines (66, 80, 81, 82), and one of the infusion lines (66, 80, 81, 82) injects the infusion solution into the extracorporeal blood line (52b) or directly into the vascular system of the subject being treated, KETON a KETON b controlling the injection to be directed (920); Or, alternatively, If the system 50 does not infuse an infusion solution containing ketone bodies, the subject being treated may a KETON band being asked to orally ingest an amount of ketone bodies or medium chain triglycerides if the patient's blood sugar level is lower than 0.05 mg / kg.

[0028] Preferably, the system (50) includes one or more of the infusion lines (66, 80, 81, 82), and the method comprises: KETONE is a concentration value that represents the concentration of ketone bodies, such as acetoacetate, β-hydroxybutyrate, or their pharma- ceutically acceptable derivatives, esters, and salts, in the infusion solution. i receiving (906); injecting the infusate through one of the one or more infusion lines (66, 80, 81, 82) into the extracorporeal blood line (52b) or directly into the vascular system of the subject being treated; and The actual blood concentration value of KETONE a KETONE b and controlling (920) the infusion pump of the infusion line to direct the

[0029] Preferably, said cancer is selected from human colon cancer and glioblastoma, as well as prostate cancer, breast cancer and liver cancer.

[0030] In a fourth aspect, the present invention provides a system computing unit (64) adapted to control an extracorporeal blood treatment system (50) for treating a subject suffering from cancer, said system computing unit comprising: a plurality of output means adapted to be operatively connected to at least one blood pump (60), at least one dialysate fluid pump (62, 68), and optionally one or more infusion pumps for controlling flow in each of the one or more infusion lines (66, 80, 81, 82); A user interface including an input means and a display means; and storage means and computing means; The system computing unit (64) determines the desired blood concentration value of glutamine, GLN badapted to receive (901); The system computing unit (64) determines the desired blood concentration value of glucose, GLUCOSE b adapted to receive (903) The system computing unit (64) calculates the desired blood concentration value of ketone bodies KETONE b adapted to receive (905); The system computing unit (64) calculates the dialysate concentration value of glutamine GLN p adapted to receive (902) The system computing unit (64) calculates the glucose dialysate concentration value GLUCOSE p adapted to receive (904); Optionally, the system computing unit (64) may generate a concentration value KETONE representing the concentration of ketone bodies, such as acetoacetate, β-hydroxybutyrate, or pharma- ceutically acceptable derivatives, esters, and salts thereof, in the fresh dialysate. p adapted to receive (907); Optionally, the system computing unit (64) may also calculate a ketone body infusion concentration value KETONE i adapted to receive (906); The system computing unit (64) calculates the actual blood concentration value of glutamine GLN a adapted to receive (909); The system computing unit (64) receives the actual blood glucose concentration value GLUCOSE a adapted to receive (910) The system computing unit (64) calculates an actual blood concentration value of a ketone body selected from the group consisting of β-hydroxybutyrate, β-hydroxybutyrate, and acetoacetate. a adapted to receive (911) The system computing unit (64) controls the blood pump (60) and the dialysate fluid pumps (62, 68) to calculate the actual blood concentration value of glutamine GLN a GLN b and the actual blood glucose concentration value GLUCOSE a Glucose b adapted to be towards or below (914); and If an infusion pump is operatively connected to the system computing unit (64), the system computing unit (64) controls the infusion pump to calculate the actual blood concentration value KETONE. a KETONE b (920) and If an infusion pump is not operatively connected to the system computing unit (64), the system computing unit (64) a and KETONE b Compared with KETONE a <KETONE b and providing a system computing unit adapted to display a message on the display informing the treated subject that he or she needs to consume an additional amount of ketone bodies or medium chain triglycerides if

[0031] In a fifth aspect, the present invention provides a dialysis solution suitable for dialysis treatment of cancer comprising ketone bodies such as acetoacetate, beta-hydroxybutyrate, or pharma-ceutically acceptable derivatives, esters and salts thereof.

[0032] Preferably, the dialysis fluid also contains a) glutamine or a glutamine-containing compound, and / or b) glucose.

[0033] Preferably, a) the concentration of glutamine or glutamine-containing compound is in an amount of 0 to 0.5 mM, and more preferably 0.05 to 0.3 mM; b) the concentration of glucose is in an amount of 0 to 6 mM, and more preferably 0.5 to 4 mM; c) The concentration of ketone bodies is in an amount of 1 to 15 mM, and more preferably 2 to 12 mM.

[0034] The above summary of the present disclosure is not intended to describe each embodiment or every implementation thereof. Advantages, together with a more complete understanding of the present disclosure, will become apparent and appreciated by reference to the following detailed description and claims, taken in conjunction with the accompanying drawings. [Brief description of the drawings]

[0035] [Figure 1] FIG. 1 is a schematic diagram of a system according to the present invention in use.

[0036] [Diagram 2] FIG. 2 is a block diagram of an exemplary extracorporeal blood treatment system including input and display devices that can utilize the user interfaces and methods described herein.

[0037] [Diagram 3] FIG. 3 is a perspective view of an exemplary dialysis system that can include the graphical user interfaces described herein.

[0038] [Figure 4] FIG. 4 is a front view of a portion of the exemplary dialysis system shown in FIG.

[0039] [Diagram 5] FIG. 5 is a schematic diagram of a portion of a system having thermal management according to one embodiment of the present invention.

[0040] [Figure 6a] FIG. 6a shows a chart of the results of Study 1. [Figure 6b] FIG. 6b shows a chart of the results of Study 1. [Figure 6c] FIG. 6c shows a chart of the results of Study 1. [Figure 6d] FIG. 6d shows a chart of the results of Study 1. [Figure 6e] FIG. 6e shows a chart of the results of Study 1. [Figure 6f] FIG. 6f shows a chart of the results of Study 1. [Figure 6g] FIG. 6g shows a chart of the results of Study 1. [Figure 6h] FIG. 6h shows a chart of the results of Study 1. [Figure 6i] FIG. 6i shows a chart of the results of Study 1. [Figure 6j] FIG. 6j shows a chart of the results of Study 1. [Figure 6j2] FIG. 6j shows a chart of the results of Study 1.

[0041] [Figure 7a] FIG. 7a shows a chart of the results of Study 2. [Figure 7b] FIG. 7b shows a chart of the results of Study 2. [Figure 7c] FIG. 7c shows a chart of the results of Study 2. [Figure 7d] FIG. 7d shows a chart of the results of study 2.

[0042] [Figure 8] 8A, 8B, and 8C illustrate the therapeutic target of the present invention.

[0043] [Figure 9] FIG. 9 is a flow chart illustrating the control algorithm of the present invention.

[0044] [Figure 10] FIG. 10 shows the growth rates of A549 and RCC4 cells in media A through C, as indicated.

[0045] [Figure 11] Figure 11 shows the abundance of lung cancer A549, renal cancer RCC4, and primary RCC cells after 3 days of culture in media A to C at 21 or 5% oxygen. Asterisks indicate significantly different values ​​as determined by 2-way ANOVA with Tukey's multiple comparison test.

[0046] [Figure 12] Figure 12 shows the results of culturing the human glioma cell line A172 under normoxia and hypoxia in media A to C supplemented with 8 mM Acac, 16 mM BOHB, or a combination of 4 mM Acac / 8 mM BOHB. 4 and 8 mM LiCl are used as controls for Acac. Significantly different values, as determined by one-way ANOVA with Sidak's multiple comparison test, are marked with an asterisk.

[0047] [Figure 13] Figure 13 shows the results of culturing the glioma cell line U118MG under normoxia and hypoxia in media A to C supplemented with 8 mM Acac, 16 mM BOHB, or a combination of 4 mM Acac / 8 mM BOHB. 4 and 8 mM LiCl are used as controls for Acac. Significantly different values, as determined by one-way ANOVA with Sidak's multiple comparison test, are marked with an asterisk.

[0048] [Figure 14] Figure 14 shows the results of culturing the glioma cell line A172 under normoxia and hypoxia in media B to C supplemented with 8 mM Acac, 16 mM BOHB, or a combination of 4 mM Acac and 8 mM BOHB. 4 and 8 mM LiCl are used as controls for 4 mM Acac / 8 mM BOHB or 8 mM Acac, respectively. Significantly different values, as determined by one-way ANOVA with Sidak's multiple comparison test, are marked with an asterisk.

[0049] [Figure 15] Figure 15 shows the results of culturing the glioma cell line U118MG under normoxia and hypoxia in media B to C supplemented with 8 mM Acac, 16 mM BOHB, or a combination of 4 mM Acac and 8 mM BOHB. 4 and 8 mM LiCl are used as controls for 4 mM Acac / 8 mM BOHB, or 8 mM Acac, respectively. Significantly different values, as determined by one-way ANOVA with Sidak's multiple comparison test, are marked with an asterisk.

[0050] [Figure 16] Figure 16 shows the results of culturing renal carcinoma cell line RCC4 under normoxia and hypoxia in media B to C supplemented with 8 mM Acac, 16 mM BOHB, or a combination of 4 mM Acac and 8 mM BOHB. 4 and 8 mM LiCl are used as controls for 4 mM Acac / 8 mM BOHB, or 8 mM Acac, respectively. Significantly different values, as determined by one-way ANOVA with Sidak's multiple comparison test, are marked with an asterisk. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0051] Exemplary systems and methods for selecting, displaying, and filtering historical data for extracorporeal blood therapies are described with reference to FIGS. 1 through 5. An extracorporeal blood treatment system can record or store one or more parameters and / or events of one or more extracorporeal blood therapies resulting in historical data. Exemplary systems and methods described herein provide a graphical user interface for displaying such historical data. In general, the historical data can include patient fluid removal data, fluid data, treatment data, anticoagulation data, pressure data, event data, configuration data, patient data, alarm data, system voltage and current data, system timing data, user interaction data (e.g., interactions with a user interface such as button presses and screen selections), and the like. In the present invention, the data can include concentrations of specific substances in the patient's bloodstream, as the system can include one or more sensors for detecting those concentrations. Detected substances can include glucose, glutamine, and other amino acids such as serine, glycine, arginine, ketones, and cytokines.

[0052] Patient fluid removal data may include total patient fluid removal data, unintentional patient fluid removal data, selected limit data (e.g., selected limit for unintentional patient fluid gain / loss over a selected period of time, such as 1 hour, 3 hours, or 24 hours), etc. Fluid data may include pre-infusion data, dialysate data, post-exchange fluid filter data, filter data, outflow data, filtered fraction data, pre-dilution data, rate per patient kilogram data, ultrafiltration rate data, ultrafiltration rate post % of blood flow data, etc. Therapy data may include prescribed outflow dose data, delivered outflow dose data, target outflow dose data, prescribed ultrafiltration rate (UFR) dose data, target UFR dose data, delivered UFR dose data, etc. Anticoagulation data may include heparin data, estimated patient citrate load data, citrate solution data, calcium solution data, replacement solution data, calcium compensation data, syringe volume delivery data, bolus delivery data, etc. Pressure data may include access line pressure data, return line pressure data, filter pressure data, transmembrane pressure (TMP) data, pressure drop across the filter (P DROP) data (e.g., pressure conditions in the blood compartment of the filter), self-test data, pressure alarm data, disconnection and occlusion limits data, stabilized pressure data, etc. Event data may include system configuration data, alarm data, settings data, therapy set data, advisory data, prescription settings data, system settings data, anticoagulation data, pressure data, patient data, mechanical data, dosage data, etc.

[0053] An exemplary extracorporeal blood treatment system 10 shown in Figure 1 can be used to perform the exemplary methods and / or processes described herein. In at least one embodiment, system 10 can be or include a machine for extracorporeal treatment of blood. System 10 can alternatively be or comprise, for example, a blood treatment device or a blood component preparation device or other medical device for fluid delivery and / or collection.

[0054] As shown, the exemplary extracorporeal blood treatment system 10 includes a computing device 12. The computing device 12 may be configured to receive input from an input device 20 and transmit output to a display device 22. Additionally, the computing device 12 may include data storage 14. The data storage 14 may provide access to processing programs or routines 16 and one or more other types of data 18 that may be used to execute the exemplary methods and / or processes for use in performing the extracorporeal blood treatment, recording historical data, filtering historical data, and displaying historical data. For example, the computing device 12 may be configured to log or record data, such as flow rates and volumes, so that a user may select and display various sets of historical data using the input device 20 (e.g., based on input from a user), and may be configured to display the historical data selected by the user using the display device 22.

[0055] The computing device 12 may be operatively coupled to the input device 20 and the display device 22, for example, to transmit data between the input device 20 and the display device 22, respectively. For example, the computing device 12 may be electrically coupled to the input device 20 and the display device 22, for example, using analog electrical connections, digital electrical connections, wireless connections, bus-based connections, etc. As described further herein, a user may provide input to the input device 20 to manipulate or modify one or more graphical depictions (e.g., windows, regions, areas, buttons, icons, etc.) displayed on the display device 22 and / or to display historical data. Additionally, various devices and apparatus may be operatively coupled to the computing device 12 for use within the computing device 12 to perform one or more extracorporeal procedures / processes, as well as the functions, methods, and / or logic described herein. As shown, the system 10 may include an input device 20 and a display device 22. The input device 20 may include any device capable of providing input to the computing device 12 to perform the functions, methods, and / or logic described herein. For example, input device 20 may include a touch screen (e.g., a capacitive touch screen, a resistive touch screen, a multi-touch touch screen, etc.), a mouse, a keyboard, a trackball, etc. Input device 20 enables a user to select and filter various historical data that is displayed on display device 22 (e.g., displaying a graphical user interface representing the historical data).

[0056] Similarly, display device 22 may include any device capable of displaying information to a user, such as a graphical user interface, to perform the functions, methods, and / or logic described herein. For example, display device 22 may include a liquid crystal display, an organic light emitting diode screen, a touch screen, a cathode ray tube display, etc. In at least one embodiment, a touch screen device may be overlaid on the display screen to allow a user to touch graphical buttons and icons on the display screen to perform certain actions.

[0057] As described further herein, display device 22 may be configured to display a graphical user interface that includes one or more regions and / or areas used to select and display raw and / or historical data for an extracorporeal blood therapy. For example, the graphical user interface displayed by display device 22 may include or display a two-dimensional graph, a data set plotted on the two-dimensional graph, one or more graphic elements or icons representing events proximate to the two-dimensional graph, a time interval selection region, an event type selection region, an event list region or view, an event information region, a historical data region, an event display region, etc.

[0058] Each graph, region, view, button, icon, panel, area, dialog, etc. may be used by a user to select and display historical data on the graphical user interface of the display device 22. As used herein, an "area" of a graphical user interface may be defined as a portion of the graphical user interface in which information is displayed or a function is performed. Regions may exist within other regions, may be displayed separately or simultaneously, etc. For example, small regions may be located within a larger region, regions may be located side by side, etc. Additionally, as used herein, an "area" of a graphical user interface may be defined as a portion of the graphical user interface that is located in a region smaller than the region in which it is located.

[0059] Processing programs or routines 16 may include programs or routines for performing computational mathematics, matrix mathematics, standardization algorithms, comparison algorithms, or any other processing necessary to perform one or more of the example methods and / or processes described herein. Data 18 may include, for example, historical data, user counts, license information, processing profiles, bitmaps, videos, calibration data, system configuration information, solution data, engineering logs, event and alarm data, system pressure, system voltage, system current, self-test sequence data, user interaction data, processing status data, monitor usage data, utilization data, software executable files, patient information, processing summary information, processing runtime data, graphics (e.g., graphic elements, icons, buttons, windows, dialogs, pull-down menus, graphic areas, graphic regions, 3D graphics, etc.), graphical user interfaces, results from one or more processing programs or routines used in accordance with the disclosure herein, or other data that may be necessary to perform one and / or more of the processes or methods described herein.

[0060] In one or more embodiments, system 10 may be implemented using one or more computer programs executing on a programmable computer, such as a computer that includes processing capability, data storage (e.g., volatile or non-volatile memory and / or storage elements), input devices, and output devices. The program code and / or logic described herein may be applied to input data to perform the functions described herein and to generate desired output information. The output information may be applied as input to one or more other devices and / or methods as described herein or applied in a known manner.

[0061] The programs used to implement the methods and / or processes described herein may be provided using any programmable language, e.g., a high-level procedural and / or object-oriented programming language suitable for communicating with a computer system. Any such programs may be stored on any suitable device, e.g., a storage medium, that is readable by a general-purpose or special-purpose program that, when read by a suitable device to perform the procedures described herein, executes on a computer system (including, e.g., a processor) for configuring and operating the computer system. In other words, in at least one embodiment, the system 10 may be implemented using a computer-readable storage medium configured with a computer program, the storage medium so configured causing a computer to operate in a specific predefined manner to perform the functions described herein. Furthermore, in at least one embodiment, the system 10 may be described as being implemented by logic (e.g., object code) encoded in one or more non-transitory media that includes code for execution, and that, when executed by a processor, is operable to perform operations such as the methods, processes, and / or functions described herein.

[0062] Similarly, system 10 may be configured at a remote site (e.g., an application server) that allows access by one or more users via a remote computing device (e.g., via a web browser) and enables the users to use functionality in accordance with the present disclosure (e.g., the users access a graphical user interface associated with one or more programs to process data).

[0063] Computing device 12 can be, for example, any fixed or mobile computer system (e.g., controller, microcontroller, personal computer, minicomputer, etc.). The exact configuration of computing device 12 is not limiting, and essentially any device capable of providing suitable computing and control capabilities (e.g., graphics processing, control of extracorporeal blood treatment equipment, etc.) can be used.

[0064] As described herein, a digital file may be any medium containing digital bits (e.g., encoded in binary, trinary, etc.) that may be readable and / or writable by computing device 12 as described herein (e.g., volatile or non-volatile memory, CD-ROM, punch cards, magnetic recordable tape, etc.).

[0065] Also, as described herein, a file in user-readable format may be any representation of data (e.g., ASCII text, binary numbers, hexadecimal numbers, decimal numbers, graphics, etc.) that can be displayed on any medium (e.g., paper, display, etc.) that can be read and / or understood by a user.

[0066] In view of the above, it should be readily apparent that the functionality described in one or more embodiments of the present disclosure may be implemented in any manner known to one of ordinary skill in the art, and thus, the computer language, computer system, or other software / hardware used to implement the processes described herein does not limit the scope of the systems, processes, or programs described herein (e.g., the functionality provided by such systems, processes, or programs).

[0067] It will be appreciated that a graphical user interface may be used in conjunction with the embodiments described herein. The user interface may provide various features that allow user input thereto, modification of input, import or export of files, or other features that may be generally suitable for use with the processes described herein. For example, the user interface may allow a user to select and filter various historical data that is displayed on a display device.

[0068] The methods and / or logic described in this disclosure, including those resulting from the system or various components, may be implemented, at least in part, in hardware, software, firmware, or any combination thereof. For example, various aspects of the techniques may be implemented within one or more processors, including one or more microprocessors, DSPs, ASICs, FPGAs, or any other equivalent integrated or discrete logic circuitry, as well as any combination of such elements, or any combination of other devices. The terms "processor" or "processing circuitry" may generally refer to any of the foregoing logic circuitry, alone or in combination with other logic circuitry, or any other equivalent circuitry.

[0069] Such hardware, software, and / or firmware may be implemented within the same device or separate devices to support various operations and functions described in this disclosure. Furthermore, any of the described elements may be implemented together or separately as separate but interoperable logical devices. The depiction of various features, for example using block diagrams, etc., is intended to highlight different functional aspects and does not necessarily imply that such features must be realized by separate hardware or software elements. Rather, functions may be performed by separate hardware or software elements or integrated within a common or separate hardware or software element. When implemented in software, functions resulting from the systems, devices, and methods described in this disclosure may be embodied as instructions and / or logic on a computer-readable medium, such as a RAM, ROM, NVRAM, EEPROM, flash memory, magnetic data storage medium, optical data storage medium, etc. The instructions and / or logic may be executed by one or more processors to support one or more aspects of the functions described in this disclosure.

[0070] The exemplary systems described herein for the selection and display of historical data in extracorporeal blood therapy, and the exemplary methods performed or used by such exemplary systems, may be generally referred to as dialysis systems. The general term dialysis as used herein includes hemodialysis, hemofiltration, and hemodiafiltration. In general, dialysis involves removing blood from the body and subjecting it to treatment equipment to separate and / or add substances thereto before returning the blood to the body. Thus, an extracorporeal blood therapy system capable of performing general dialysis is described herein with reference to the exemplary extracorporeal blood therapy systems of FIGS. 2 through 4. Other systems may benefit from the systems, methods, and devices described herein, and the disclosure is not limited to a particular fluid treatment system.

[0071] In the schematic diagram of Figure 2, an exemplary extracorporeal blood treatment system 50 generally includes a blood tubing circuit 52 including an arterial line 52a and a venous line 52b connectable to a patient's vascular system. The device includes a filtration unit 58 having a primary chamber (blood chamber) and a secondary chamber (dialysate chamber) separated by a semi-permeable filtration membrane 59. An inlet of the primary chamber is connected to a blood draw line or arterial line 52a. Similarly, an outlet of the primary chamber is connected to a blood return line or venous line 52b.

[0072] The inlet of the secondary chamber is connected to a fresh dialysate fluid supply line 54b, which is connected to a source 74 for providing fresh dialysis solution. The outlet of the secondary chamber of the filtration unit 58 is connected to a dialysis solution or spent dialysate line 54a, which carries the spent dialysis solution to an outlet connector 73.

[0073] In the present invention, filtration unit 58 comprises a membrane 59 that differs from conventional hemodiafiltration membranes in that it is configured to remove relatively small compounds from the blood in blood tubing circuit 112. The membrane is configured to have a molecular weight cut-off (MWCO) of 50 kDa or less, or even 40 kDa or less (such as 30 kDa or less, 10 kDa or less, 5 kDa or less, or 2 kDa or less).

[0074] The flow of blood through blood lines 52a, 52b and filtration unit 58 is governed by a blood pump 60 located in arterial line 52a. Similarly, the flow of fresh dialysate fluid from a source 74 through filtration unit 58 to an effluent collector 73 by a dialysate fluid pump 68 in supply line 54b, the pressure in dialysate fluid line 54 is governed by a pressure relief valve in spent dialysate line 54a. Alternatively, instead of a pressure relief valve, a second pump 62 can be included in spent dialysate line 54a.

[0075] There may also be one or more infusion lines 66, 80, 81, 82 connected to the venous portion of the blood line 52b. In some embodiments, one or more of these infusion lines are adapted to be directly connected to the patient's vascular system (not shown). Each of the one or more infusion lines 66, 80, 81, 82 may be equipped with a separate pump. In one embodiment, an infusion solution containing ketone bodies or ketone body derivatives may be infused by such infusion lines.

[0076] The system computing unit 64 is provided to communicate with the blood pump 60, the dialysate fluid pump 68, and one or more pumps in the one or more infusion lines 66, 80, 81, 82, and pressure relief valves or additional dialysate fluid pumps 68, providing control of these devices during use. In an alternative embodiment, the system computing unit 64 provides the user with appropriate configuration data via a graphical user interface for the pumps in the one or more infusion lines 66, 80, 81, 82. The system computing unit also communicates with input means for the provision of information and instructions to the system processing unit 64. The input means may comprise a graphical user interface, such as one that can be controlled using a touch screen configuration. In some embodiments, the input means may include a keyboard. In some embodiments, the input means may include one or more sensors for detecting concentrations of various substances or conditions in the patient's blood and / or in the used dialysate.

[0077] For example, a sensor may be provided to detect the concentration of one or more of amino acids such as glutamine, serine, glycine, arginine, glucose, ketones, and cytokines in the subject's blood. In particular, such a sensor should be adapted to detect the concentration of one or more of glutamine, glucose, and ketone bodies in the subject's blood. Such a sensor S, 91, 93 may be provided in the blood line 52 or by use of a separate device that may be placed elsewhere in the patient's body S, 90. To the extent that the sensor is deployed, it provides an indication of the actual blood concentration of the intended analyte to the system processing unit 64 (directly or via additional input means). This provision may be made periodically or substantially continuously during processing.

[0078] Suitable sensors and assays for analyzing glutamine, glucose, and ketone bodies are known in the art. For example, a glutamine sensor is disclosed in US Patent No. 4,780,191. Examples of glutamine assays are disclosed in US Patent No. 9,995,750 and US Patent Publication No. 2016 / 168619. Examples of sensors and assays for determining the concentration of ketone bodies are disclosed in US Patent No. 8,532,731, WO 2016 / 178823, US Patent No. 5,326,697, and US Patent No. 5,618,686. Examples of glucose sensors and assays are disclosed in US Patent Publication No. 2019 / 328288, US Patent Publication No. 2018 / 128767, and US Patent Publication No. 2011 / 105871.

[0079] Additionally, the patient's blood levels of one or more of the amino acids, such as glutamine, serine, glycine, and arginine, as well as glucose, ketones, and cytokines (preferably at least those of glucose and glutamine) may be measured by collection and separate analysis (e.g., laboratory analysis) of the patient's blood. This method may be particularly relevant during long-term processes, but may be deployed during any process depending on the proximity and speed of analytical facilities.

[0080] In another embodiment, one or more sensors S, 92 may be optionally included in the outlet line 54b, which may detect the concentration of one or more of glucose, amino acids such as glutamine, serine, glycine and arginine, ketones or cytokines, as appropriate. The concentration of the analyte of interest measured in the outlet line may be used to determine a representative concentration of the analyte of interest in the patient's blood, such as by the method described in EP 2377563, which is incorporated herein by reference.

[0081] When cells in the body are exposed to higher than normal temperatures, changes occur within the cells. Treatment can be localized (tumor only), regional (extremities, etc.), or whole-body hyperthermia, depending on the extent of the area to be treated. Extremely high temperatures can cause cancer cells to transition to necrosis / apoptosis (thermal ablation), but high temperatures can also cause damage or induce apoptosis / necrosis in normal cells. Therefore, hyperthermia must be carefully controlled.

[0082] Hyperthermia is a promising method to improve cancer treatment and, today, is cumbersome to perform, since it requires special equipment. Many clinical trials on hyperthermia for cancer treatment are ongoing. As suggested, extracorporeal circuits are suitable to induce and control hypothermia in patients. Increasing blood temperature simultaneously with extracorporeal blood volume treatment would be an excellent combination therapy that could enhance the effect of the altered blood volume.

[0083] With a blood flow of 300 ml / min and a return blood temperature of 43 degrees, an effect of about 120 watts is delivered to the patient and body temperature is easily raised. Blood temperature can be raised to 45°C for a short period of time without substantial damage to the blood.

[0084] It may be necessary to cool the patient not only to terminate the treatment, but also to adjust the treatment too effective. Cooling leads to a decrease in the metabolic rate of normal and cancer cells, but then also in oxygen consumption. The mentioned changes lead to the protection of normal healthy cells, but also to the weakening of cancer cells, for example, to conventional cancer treatments, but also to cancer dialysis, and to the reduction of glucose, glutamine, and oxygen. Cooling also reduces the harmful side effects to conventional cancer treatments administered to the patient, but also allows them to withstand more aggressive treatments of cancer dialysis and conventional cancer treatments. The present drawing does not show means for cooling or heating the blood, but such means are well known to those skilled in the art and are frequently used in connection with some types of extracorporeal blood treatments, such as continuous renal replacement therapy (CRRT).

[0085] Figures 8A, 8B and 8C illustrate the therapeutic goals and principles of the present invention. Each figure discloses an example of a normal state for the concentration of a particular blood component. Figure 8A shows that at the start of treatment, patients typically have glutamine GLN in the range of 0.20 to 0.8 mM. a During treatment, the actual blood concentration of glutamine is within the range of 0.1 to 0.5 mM, and the desired value GLN is within the range of 0.15 to 0.3 mM. b 8B is a standardized method for determining whether patients typically have a glucose level in the range of 4 to 8 mmol / l at the start of treatment. a During treatment, the actual blood concentration of glucose is increased to the desired value, which is typically in the range of 2 to 4 mmol / l. bFinally, FIG. 8C shows that the blood initially contains very little ketone bodies, such as β-hydroxy-butyric acid or pharma- ceutically acceptable salts or esters thereof, such as the sodium salt. Thus, the actual value of the concentration of ketone bodies in the patient's blood, KETONE a is approximately 0. Usually, new dialysis fluid contains no or only small amounts of ketone bodies. During treatment, the blood concentration of such ketones is increased to a desired value in the range of 1 to 15 mmol / l, such as in the range of 2 to 12 mM, by infusion of a solution of ketone bodies and / or ketone body derivatives. b can rise to.

[0086] In one embodiment, the actual blood concentration of glutamine GLN a , and / or actual blood glucose concentration GLUCOSE a is the desired value GLN b and / or GLUCOSE b These actual blood levels of GLN may then be below a and / or GLUCOSE a The desired level of GLN can be achieved by infusion of a solution containing glucose and / or glutamine or a pharma- ceutical acceptable glutamine-containing compound. b and / or GLUCOSE b It can be increased to

[0087] 9 discloses a flow chart of an example of an algorithm 900 of a control process according to the present invention. Before starting the process, the system computing unit 64 is adapted to receive the process target concentrations or desired blood concentrations of the compounds of interest. Typically, these process target concentrations are input using a user interface.

[0088] Thus, in step 901, the system computing unit 64 receives a desired blood concentration value of glutamine, GLN b Receive.

[0089] In step 903, the system computing unit 64 receives a desired blood concentration value of glucose, GLUCOSE b Receive.

[0090] In step 905, the system computing unit 64 receives a desired blood concentration value of ketone bodies, KETONE b Receive.

[0091] Before starting the process, the system computing unit 64 is also adapted to receive concentration values ​​in the new dialysate for the above mentioned important components. Typically, these concentration values ​​are also entered using the user interface.

[0092] Thus, in step 902, the system computing unit 64 calculates the concentration value of glutamine in the new dialysate GLN P Receive.

[0093] In step 904, the system computing unit 64 calculates the concentration value of glucose in the new dialysate, GLUCOSE P Receive.

[0094] In step 907, the system computing unit (64) receives a concentration value KETONE representing the concentration of ketone bodies, such as acetoacetate, β-hydroxybutyrate or pharma- ceutically acceptable derivatives, esters and salts thereof, in the fresh dialysate. p The signal is adapted to receive

[0095] In step 906, the system computing unit 64 calculates the concentration value of ketone bodies in the infusate that is infused into the extracorporeal blood line (52b) or directly into the vascular system of the subject / patient being treated. i Receive.

[0096] Before starting the process, and optionally during the process, the system computing unit 64 is adapted to receive actual concentration values ​​determined from the patient's blood. These concentration values ​​can be obtained after taking a blood sample and subsequently analyzing it in a separate analysis unit. The concentration values ​​are then entered manually via a user interface. In some embodiments, the system computing unit is connected to one or more such separate analysis units, and thus can receive data directly therefrom. In some embodiments, the blood circuits 52a, 52b and / or the dialysate circuits 54a, 54b may comprise suitable sensors S, 90, 91, 92, 93 connected to the system computing unit 64, which receives the data. The system computing unit 64 typically receives the actual values ​​GLN, which have been just received. a , GLUCOSE a , and KETONE a Control processing based on the

[0097] Thus, in step 908, the system computing unit 64 begins processing.

[0098] In step 909, the system computing unit 64 receives the actual blood concentration value of glutamine, GLN, from the patient. a The signal is adapted to receive

[0099] In step 910, the system computing unit 64 receives an actual blood concentration value of glucose, GLUCOSE, from the patient. a The signal is adapted to receive

[0100] In step 911, the system computing unit 64 receives the actual blood concentration value of ketone bodies, KETONE a The signal is adapted to receive

[0101] In step 912, the system computing unit 64 configures the blood pump 60 and the dialysate fluid pumps 62, 68 with the GLN a GLN b To control the amount of heat generated by the heat source so that the heat generation rate is toward or below the specified value.

[0102] At the same time, in step 914, the system computing unit 64 controls the blood pump 60 and the dialysate fluid pumps 62, 68 to a GLUCOSE b To control the amount of heat generated by the heat source so that the heat generation rate is toward or below the specified value.

[0103] At a simultaneous step 916, the system computing unit 64 a Monitor and GLN a GLN b If the blood glucose level is lower than 100 mg / mL, the system computing unit initiates and maintains the infusion of a composition containing glutamine or a glutamine-containing compound into the extracorporeal blood circuit 52a, 52b.

[0104] At the same time, in step 918, the system computing unit 64 a Monitor and GLUCOSE a GLUCOSE b If the glucose level is lower than 0.5, the system computing unit initiates and maintains the infusion of the glucose-containing composition into the extracorporeal blood circuit 52a, 52b.

[0105] At the same time, in step 920, the system computing unit 64 a Monitor and K a K b If the blood pressure is lower than 100° C., the system computing unit initiates and maintains an infusion of a composition containing ketone bodies into the extracorporeal blood circuit 52a, 52b or directly into the vascular system of the subject being treated.

[0106] In some embodiments, the levels of other substances in the blood can be controlled. For example, lowering the normal levels of amino acids such as serine, glycine, and arginine has been found to be beneficial.

[0107] 3-4, an exemplary extracorporeal blood treatment system 110 capable of implementing the processing and graphical user interface described herein generally includes a blood tubing circuit 112 having first and second tubing segments 114 and 116, both connected to a patient's vascular system via an access device 117 and a return device 119, respectively. Devices 117 and 119 may be cannulas, catheters, winged needles, etc., as will be understood by those skilled in the art. Tubing segments 114 and 116 are also connected to a filtration or processing unit 120. In dialysis, filtration unit 120 is a dialyzer, often also referred to as a filter.

[0108] Numerous other component devices of the blood circuit 112 are also included, such as pressure sensors 127, 128, 154, 129. Additional sensors may be provided to monitor concentrations of glucose and / or glutamine, ketones (such as hydroxybutyrate (BHB) acetoacetate and acetone), and / or cytokines (such as tumor necrosis factor (TNF) (e.g., TNF-α), interleukins (e.g., IL-6)). However, as noted above, the sensors may be located in direct contact with the patient rather than in the blood circuit 112. If present, the sensors are operably connected to the computing device 12 by wireless or physical connections.

[0109] As shown diagrammatically in FIG. 5, the blood circuit 112, including the blood access line 114 and the blood return line 116, may also include a thermal management system 500 for heating or cooling the blood in the blood circuit 112. The thermal management system 500 is operatively connected to the computing device 12, 64. Such a thermal management system may be used to heat the blood returning to the patient, such as to about 37° C. Such a system may also be used to cool the returning blood to 20° C. or to warm the patient to a temperature between 38 and 40° C., such as by raising the temperature of the returning blood to 43° C. Additionally, the dialysate circuit may also include a second thermal management system 501 to ensure that the blood reaches the desired temperature after passing through the blood filter 120.

[0110] Also shown in Figures 3 and 4 is the dialysate fluid or filtrate side of the system 110, which generally includes a dialysate fluid circuit 140 having first and second dialysate fluid tubing segments 141 and 142. Each of these tubing segments is connected to the filtration unit 120 on the opposite side of the membrane to the blood circuit 112 segments 114, 116. In these Figures 3-4, a respective fluid pump 144, 146 is operatively associated with each of these tubing segments 141 and 142.

[0111] The first tube segment 141 is also connected to a dialysate fluid source (e.g., fluid bag 149), which may contain electrolytes or other treatment compounds premixed therein. The second tube segment 142 is connected to a waste collection device (e.g., a waste container such as bag 153). A pressure sensor 154 may also be disposed within the second dialysis fluid tube segment 142.

[0112] 3-4 show a general system as a base model for many dialysis procedures. Additional fluid lines, circuits, and elements can be added (or removed) to increase treatment options. In particular, the present invention can provide additional lines to supply ketones (e.g., hydroxybutyrate (BOHB), acetoacetate, and / or acetone) to the patient (such as by addition to the blood circuit 112). Supplying ketones to the patient is important because it reduces the need for the patient to be in a state of diet-induced ketosis prior to the start of treatment. In embodiments where a separate supply of ketones is not provided, the fluid source bag 149 can also contain one or more ketones (such as sodium BOHB) in solution to diffuse through the membrane into the blood circuit.

[0113] One or more of the dialysate fluid source 149, waste container 153, and replacement fluid container 168 may be provided on a scale 400 in operative communication with the computing device 12. An optional additional source of ketone may also be provided on such scale 400. This allows the mass of fluid in each container to be monitored during use to provide an accurate record of the amount of each fluid used or collected.

[0114] 3-4, system 110 includes an extracorporeal blood control device 160 that provides a number of processing options that may be controlled and / or monitored via a control / display screen 161 (e.g., a control device or controller provided in system housing 193). Touch screen controls may be incorporated herein and / or other conventional knobs or buttons (not shown) may be used (e.g., a graphical user interface may be displayed via the touch screen as described herein). Other, more detailed information regarding the exemplary device 160 may be found in, among other places, U.S. Pat. Nos. 5,679,245, 5,762,805, 5,776,345, and 5,910,252, US Pat. Nos. 5,821,333, 5,821,333, 5,821,333, and 5,910,252, US Pat. Nos. 5,910,252 ... US Pat. No. 5,399,623 can be found in U.S. Pat.

[0115] For example, a typical dialysis treatment procedure carried out using the apparatus described with reference to Figures 3 and 4 will be generally described for purposes of illustration. Initially, blood is removed from a patient 118 via an access device 117, for example by a blood pump 124, and flows through an access line 114 to a filter 120. Filter 120 processes the blood according to a selected one or more of a number of extracorporeal blood treatment profiles (e.g., selected and controlled via a screen interface 161 of a controller 160).

[0116] The treatment profile also includes a reduction in glutamine and glucose in the patient's blood. The concentration of glutamine is reduced to a value in the range of 0.1 to 0.5 mM, and preferably to a value in the range of 0.15 to 0.3 mM. The blood concentration of glucose is reduced to a concentration in the range of 1 to 6 mM, and preferably to a concentration in the range of 2 to 4 mM. This treatment has a much more pronounced adverse effect on cancer cells than on healthy cells in the body, since glycolysis and glutaminolysis pathways are enhanced in many cancer cells. While glycolysis is enhanced to meet the increasing energy demands of cancer cells, glutaminolysis is also enhanced in many cancer cells, and can provide biosynthetic precursors, but also plays an important role in maintaining reactive oxygen species (ROS) hemostasis. Forcing cancer cells into apoptosis by increasing the production of ROS in cancer cells is an important target for both radiation therapy and chemotherapy. Finally, glutamine may act as a source of ATP during low levels of glucose. In some embodiments, the treatment profile ensures that the patient's nutritional needs can be met by providing an appropriate parenteral nutrition composition to the blood line or as a separate infusion directly into the patient's vascular system. In some embodiments, the blood concentration of ketone bodies is maintained at a value within the range of 1 to 15 mM, and preferably within the range of 2 to 12 mM, during treatment. Although the patient is expected to generate their own ketone bodies when exposed to such low blood glucose concentrations (e.g., from consumed or infused lipid or body fat stores), it may take time for the biological process to begin to generate sufficient amounts of ketone bodies. The introduction of ketone bodies during the treatment described herein ensures that the patient has a sufficient energy source in a timely manner to continue vital functions, even if blood glutamine and blood glucose concentrations decrease at an unnaturally fast rate.

[0117] In certain treatments, particularly those in which high blood ketone body concentrations are maintained, one or more medications are provided to the patient to help lower blood glucose concentrations. Such glucose-lowering agents preferably include biguanides, α-glucosidase inhibitors, SGLT2 inhibitors, and dopamine agonists. Such medications may be provided by the system by inclusion in the dialysate fluid source 149, additional ketone sources (if present), or as additional infusions provided to the blood circuit 112 or the patient.

[0118] An example of a biguanide is metformin. An example of an α-glucosidase inhibitor includes acarbose or miglitol. An example of an SGLT2 inhibitor includes canagliflozin, dapagliflozin, and empagliflozin. An example of a dopamine agonist includes bromocriptine.

[0119] In some preferred treatments, an antiglycolytic agent may be provided to the patient to further inhibit glycolytic activity in the tumor cells. Such agents may be supplied by the system by inclusion in the dialysate fluid source 149, in the additional ketone source (if present), or as an additional infusion delivered to the blood circuit 112 or the patient.

[0120] Following processing, the system returns the treated or processed blood to the patient 118 via a return line 116 and a return device 119 inserted into or otherwise connected to the vascular system of the patient 118 .

[0121] The blood flow paths to and from the patient 118, including the access device 117, the access line 114, the blood pump 124, the filter 120, and the return line 116 and return device 119 back to the patient, form the blood flow circuit 112. Pressure sensors may be used to sense various pressures within the system 110. For example, a pressure sensor 127 may be connected to the access line 114 and allow monitoring of the fluid pressure within the access line 114, and a second pressure sensor 128 may be connected to the blood circuit 112 between the first blood pump 124 and the blood inlet to the filter 120 and may be used to detect and monitor the pressure of the blood supplied to the inlet of the filter 120.

[0122] The system 110 further includes a degassing chamber 125 in the return line, providing a transport path that acts like a vortex to push air out of the blood. To prevent an air / blood interface, post-filter change solution can be added to the degassing chamber on top of the blood. A degassing chamber monitoring line 191 can connect the degassing chamber 125 to an internal pressure transducer in the system housing 193 using a connecting device, such as a return pressure port 129. This allows for monitoring of the return pressure and removal of air from the degassing chamber as needed. A return clamp 131 connected to the blood circuit 112 selectively allows or stops the flow of blood through the blood circuit 112 (e.g., the return clamp 131 can be activated whenever air is detected in the blood by the air bubble detector 126).

[0123] Additionally, a pump 162 can be connected to an anticoagulant container 164 to deliver anticoagulant via an anticoagulant line 165 to the blood in the tube segment 114, and a pump 166 can deliver replacement fluid from a replacement fluid container or bag 168 via a replacement fluid line 170. A secondary flow circuit 140 is also shown in Figures 3-4 and interacts with the filter 120. The secondary flow circuit 140 is connected to the secondary chamber of the filter 120. Substances removed from the blood extracorporeally are removed from the secondary chamber of the filter 120 through the outlet tube segment 142 of the secondary flow circuit 140, and substances added extracorporeally to the blood are transferred into the filter 120 through the inlet tube segment 141 of the secondary flow circuit 140.

[0124] The secondary flow circuit 140 generally includes a fluid source such as a bag 149, an inlet fluid line 141, a third pump 144, a secondary chamber of the filter 120, a waste fluid line 142, a pressure sensor 154, a fourth pump 146, and a waste collection device such as a container 153. The fluid source bag 149 may contain a sterile dialysis fluid, generally isotonic to blood, from which blood impurities diffuse through the semipermeable membrane of the filtration unit 120. The fluid source bag may also contain one or more ketones in solution to diffuse through the membrane into the blood circuit.

[0125] A pump 144 is connected to the inlet fluid line 141 for delivering dialysate fluid from a dialysate fluid source 149 to an inlet to the filter 120. A waste collection container 153 is provided for collecting or receiving materials from the blood transferred across the semipermeable membrane in the filter 120 and / or for receiving spent dialysate fluid after passing through the filter 120. A fourth pump 146 is connected to the waste collection line 142 for moving spent dialysate from the filter 120 to the waste collection container 153. A pressure sensor 154 may also be disposed in the waste collection line 142 for the purpose of monitoring the pressure in the secondary chamber of the filter 120.

[0126] The filtration unit 120, flow tubing lines, and other elements in the primary and secondary flow circuits 112 and 140 described herein (e.g., excluding the pump and possibly some other items) may be formed as an integrated replaceable unit (e.g., an extracorporeal blood set). This integrated replacement unit may be referred to herein as a "treatment set." An example of such a treatment set, or integrated replaceable unit, is described in detail in U.S. Pat. No. 5,441,636, entitled "Integrated Blood Treatment Fluid Module" (see also U.S. Pat. No. 5,679,245, entitled "Retention Device for Extracorporeal Treatment Apparatus").

[0127] Depending on the system configuration, treatment sets may be available for use in performing different treatments. In general, as can be seen from FIGS. 3 and 4, an integrated tubing and filter module (identified by reference number 172) includes the filter 120 and all of the above-mentioned tubing and associated elements connectable to the device 160. For example, the filter and tubing may be held on a plastic support member 174 connectable to the device 160 (e.g., connectable to the system housing 193 of the device 160). The treatment set may also include sensors for monitoring the concentration of glucose and / or glutamine, ketones (such as hydroxybutyrate (BHB), acetoacetate, and acetone), and / or cytokines (such as tumor necrosis factor (TNF) (e.g., TNF-α)), interleukins (e.g., IL-6). Such sensors may be configured to monitor the concentration of the listed components in the blood circuit or by directly interfacing with the patient's body.

[0128] When in an operative position connected to device 160, the flexible fluid conducting tubing lines to and from filtration unit 120 are held in operative pump communication loops for operative contact with the peristaltic pumping members of pumps 124, 144, 146 and 166, causing fluid to flow through primary (blood) and secondary (dialysate fluid) circuits 112 and 140. Module 172 contains filter 120 and all tubing lines and associated flow elements, and can be disposed of after use.

[0129] The peristaltic pumping members of pumps 124, 144, 146, and 166 may be fixedly disposed on device 160 (without disposable tubing loop elements) and may be reusable. Generally, electrical, mechanical, or electromechanical components may also be fixedly disposed in or on device 160 (e.g., connectable to system housing 193 of device 160). Examples of such elements include display screen 161 (e.g., touch screen), air bubble detector 126, line clamp 131, and connection devices for coupling to pressure sensors used to implement pressure sensors 127, 128, 129, 154, etc. Couplings may also be provided for any sensors that are required or preferred.

[0130] As discussed above, the access device 117 and the return device 119 can include a catheter. In some embodiments, the catheter can include an occlusion catheter, such as a balloon occlusion catheter. This configuration allows the access device 117 and the return device 119 to be delivered to the site of the tumor (e.g., via femoral artery or venous entry) as shown in Figure 4. This provides for a localized reduction in blood glucose concentrations around the tumor, thereby potentially reducing blood glucose and / or glutamine concentrations to even lower levels.

[0131] Reference example 1 The sensitivity of different human cancer cell lines to the presence of glucose, glutamine, and ketones in the cell culture medium and the simultaneous depletion of selected nutrients was investigated to mimic the conditions obtained during cancer dialysis.

[0132] Study 1 was performed on a selection of human cancer cell lines formed from renal cell carcinoma, colon carcinoma, and glioblastoma. The first study was the effect on cell viability of growth in the presence of increasing concentrations of the ketone β-hydroxybutyrate, with simultaneous limitation of glucose and glutamine levels. The addition of citrate to the cell culture medium was also tested. After culturing the cells under these conditions for 3 days, cell viability was measured. In the first study, the main effect on cell viability was seen when glutamine was depleted from the culture medium.

[0133] material and method Cell culture conditions Cell lines formed from human colon carcinoma (HCT15, NCI-H508, and COLO205), renal cell carcinoma (769-P, 786-0, and RCC4), and glioblastoma (LN-18, A-172, and U-118MG) were selected for analysis. All cell lines were obtained from the American Type Culture Collection (ATCC, LGC Standards, UK), except for RCC4 and HCT15, which were purchased from Sigma-Aldrich (Merck, Germany). In addition, primary human renal cell carcinoma (RCC) cells isolated from nephrectomized patients were included in the study. Culture conditions were as recommended by the American Type Culture Collection (ATCC), with cells grown in DMEM medium supplemented with 1 mM sodium pyruvate, which was also added to RPMI-1640 medium to maintain closer conditions.

[0134] 769-P, RCC4, LN-18, A-172, U-118MG and primary RCC cells were cultured in DMEM high glucose medium, while 786-0 HCT15, NCI-H508 and COLO205 were cultured in RPMI-1640 medium according to the recommendations from ATCC. Both media were supplemented with 1% penicillin-streptomycin and 10% bovine calf serum. Cells were expanded and aliquots were frozen according to standard procedures.

[0135] The optimal seeding density was determined for each cell line in 96-well plates by following the "Protocol for optimizing cell seeding density to ensure log-phase growth." The protocol is as follows: - Prepare single cell suspensions and measure cell count / viability. · Cells were diluted to approximately 160,000 cells / mL in complete medium. 200 μL of cells were added to the top row of a 96-well plate. All other wells were dispensed with 100 μL of complete medium. A few medium-only control wells were needed on each plate to act as blanks. Using a 12-well channel pipette, the cell preparation was repeatedly diluted 1 in 2 across the plate, i.e., in the bottom row, 100 μL cells were added to 100 μL medium. Then, 50 μL of complete medium was added to all wells. The plate was covered. Plates were incubated overnight at 37°C and 5% CO2. · 50 μL of fresh medium was added to plate wells to a final volume of 200 μL and incubated at 37°C, 5% CO2 for 72 hours. Viability was measured using the Cell Titer Glo assay according to the manufacturer's protocol. The cell concentration at which logarithmic growth was achieved was determined by plotting log cell number against luminescence intensity. The Cell Titer-Glo luminescent cell viability assay (Promega) was used as a viability readout.

[0136] Study 1 For each cell line, the optimal number of cells determined above was seeded in 96-well plates on day 0. The next day, cells were washed with PBS and the medium was changed to DMEM (Fisher Scientific) or RPMI-1640 medium (Saveen Werner) without glucose or L-glutamine, with the addition of nutrients as outlined in Table 3 and in the file "Plate Overview". Three wells were treated per condition. After 3 days of culture in medium of the test condition, medium was changed daily and cell viability was measured using the Cell Titer-Glo viability test. Experiments were repeated three times for each cell line.

[0137] [Table 1]

[0138] [Table 2]

[0139] [Table 3]

[0140] The matrix indicates the different combinations of growth conditions used in Study 1. *The amount of glucose is shown as a percentage of the concentration present in standard medium for each cell line. Where indicated, 1 mM citrate was added to the medium. The indicated nutrients were added to DMEM (Fisher Scientific) or RPMI-1640 medium (Saveen Werner) without glucose or L-glutamine.

[0141] [Table 4]

[0142] [Table 5]

[0143] The results of Study 1 are shown in the chart shown in Figure 6. A clear correlation is shown between the reduction in glutamine and cell culture medium present and the reduction in cell proliferation.

[0144] Study 2 As mentioned above, in study 1, the culture conditions recommended by ATCC were followed. However, pyruvate is a potential energy source that may affect the results. Therefore, in study 2, the same culture conditions as in study 1 were tested on two cell lines, A172 (glioblastoma) and RCC4 (renal cell carcinoma), in DMEM medium without the addition of sodium pyruvate. The results are shown in Figure 7. As in study 1, a clear association is shown between the reduction in glutamine and cell culture medium present and the reduction in cell proliferation. However, the results are much more pronounced when pyruvate is not present in the cell culture medium. Also, increasing concentrations of BOHB ketones seem to inhibit cell proliferation.

[0145] All patents, patent documents, and references cited herein are incorporated in their entirety as if each were individually incorporated. This disclosure is provided with reference to exemplary embodiments and is not intended to be construed in a limiting sense. As previously mentioned, those skilled in the art will recognize that various other exemplary applications can use the techniques described herein to take advantage of the beneficial properties of the apparatus and methods described herein. Various modifications of the exemplary embodiments, as well as additional embodiments of the present disclosure, will become apparent upon reference to this description.

[0146] Example 2 Consideration Design Growth medium To study the effect of a nutrient-restricted ketogenic environment on cancer cell growth in vitro, three different cell culture media were formulated. Medium A was the complete RPMI1640 medium in which cell lines are routinely cultured. Medium B was used as an approximation of conditions found in normal human serum. Levels of glucose, glutamine, serine, glycine, and arginine were adjusted to match normal physiological levels found in human serum. These nutrients were selected based on their reported use as energy sources and their effect on the metabolic state of cancer cells. Medium C was used to emulate ketogenic nutrient-restricted cancer dialysis conditions. Here, the levels of selected nutrients were reduced to half of the physiological levels in Medium B and supplemented with the ketone body BOHB.

[0147] The composition of each medium is described in Materials and Methods and in Tables 5 and 6.

[0148] Oxygen levels Human cancer cell lines are typically formed and cultured at atmospheric oxygen levels (21% O2), but physiological oxygen levels within tissues are much lower, varying from 3 to 13% [Ward,Biochim Biophys Acta 2008;1777:1-14]. Within the tumor microenvironment, the rapid growth rate of cancer cells combined with an often malformed and defective vasculature often results in hypoxic regions with oxygen levels ranging from 0 to 5%. To investigate the effect of oxygen levels on energy metabolism [Xie et al.,J Biol Chem 2017;292:16825-16832], and to further mimic physiological conditions in vivo, the growth of cancer cell lines in media A, B, and C was examined both at ambient 21% O2 and at the more physiological 5% O2.

[0149] Ketones The ketone bodies acetoacetate (Acac), BOHB, and acetone are produced by the liver during fasting or starvation. BOHB is the major ketone body in mammals, with Acac accounting for approximately 20%. The majority of published in vitro studies investigating the effects of ketones on cancer cells have focused primarily on BOHB, although there are studies suggesting different effects of the addition of Acac compared to BOHB [Vallejo et al., J Neurooncol 2020;147:317-326]. Acac has also been included in this review to further mimic the in vivo ketogenic state in which both ketones are present and to explore the possible differential effects of BOHB and Acac.

[0150] material and method cell line All cell lines were purchased from ATCC (ATCC, LGC standards), except for RCC4, which was from Sigma-Aldrich (Merck). Primary human renal cell carcinoma cells were isolated from nephrectomies performed at Sahlgrenska University Hospital, Gothenburg, Sweden, with patient consent and with permission from the local ethical committee. Optimal seeding density was determined for each cell line in 96-well plates cultured for 3 days in standard cell culture medium.

[0151] Culture conditions and supplements Cells were maintained in RPMI-1640 medium (31870-025 GIBCO) supplemented with 10% serum, 200 mM L-glutamine, and 1% penicillin-streptomycin (PEST) in a humidified chamber at 37°C and 5% CO2. For hypoxic conditions (5% O2), cells were maintained in a Galaxy 14S CO2 incubator (Eppendorf) with O2 levels adjusted to 5% using N2.

[0152] Media A, B, and C were prepared as follows. Medium A: RPMI 1640 (31870-025, GIBCO) supplemented with 1% PEST, 200 mM L-glutamine, and 10% dialyzed serum. Dialyzed serum was used to reduce the amount of small molecules such as amino acids.

[0153] Media B and C were prepared from RPMI1640 modified medium powder without L-glutamine, glucose, and amino acids (R9010-01, US Biological Life Sciences). For 1 L of medium, 7.4 g of powder was dissolved in 900 ml of sterile water without heating, and 2 g of sodium bicarbonate was added. The amino acids listed in Table 5 were added at the same concentrations as in complete RPMI1640 medium (Table 5). After all additions, the medium was sterilized by filtering through a 0.22 μm membrane and divided into two bottles.

[0154] In medium B, to mimic physiological conditions, the levels of glutamine, serine, glycine, arginine, and glucose were set to the median of measured levels in human serum based on data from Mayo Clinic Laboratories (https: / / www.mavocliniclabs.com / test-catalog / Clinical+and+Interpretive / 9265).

[0155] To model cancer dialysis conditions in medium C, the levels of these nutrients were reduced to 50% of physiological levels. For medium A, 1% PEST and 10% dialyzed serum were added to media B and C. The concentrations of selected nutrients in media A to C are summarized in Table 6. Sodium pyruvate, commonly added to cell culture media, was not present in any of the media used.

[0156] [Table 6]

[0157] [Table 7]

[0158] Amino acids and other additives were purchased from Sigma Aldrich.

[0159] After all nutrients were added, the pH was measured and the pH values ​​were as follows: complete RPMI 1640 with 10% non-dialysed FBS, 1% PEST and 200 mM L-glutamine was pH 7.78, medium A was pH 7.56, medium B was pH 7.62 and medium C was pH 7.57.

[0160] Stock solutions of DL-β-hydroxybutyric acid sodium salt (H6501, Sigma Aldrich) and lithium acetoacetate (A8509, Sigma Aldrich) were prepared in water, sterile filtered, aliquoted, and stored at −20° C. Lithium chloride (L7026, Sigma Aldrich) was used as a control for lithium addition to Li-Acac.

[0161] Viability assay The CellTiter-Glo Luminescent Cell Viability Assay (Promega) was used as a readout for cell number according to the manufacturer's instructions. For the experiments shown in Figures 12 and 13, duplicate plates were seeded and processed. One set of plates was used for lactate measurements (see below) and for collection of medium for the CellTiterGlo assay. The other set of plates was frozen at -80 °C at the end of the experiment. The frozen plates were intended for the CyQuant Cell Proliferation Assay (Thermo Fisher), which measures the amount of DNA per well. Analysis of cell amount by both the CellTiterGlo and CyQuant assays ensures that effects of culture conditions on viability or proliferation rate are not masked by concomitant changes in ATP levels per cell.

[0162] Collection of culture medium for lactate measurement In the experiments shown in Figures 12 and 13, cell culture medium was collected on day 3, transferred to a new 96-well plate, and frozen at -80°C. This medium could be used to analyze the amount of lactate excreted as a measure of metabolic status. Several kits for lactate measurement are available, for example the Lactate-Glo assay (J5021, Promega) is designed for use in assays in the presence of serum.

[0163] result Example 2 was designed to answer the following question. -Is the growth of selected cancer cell lines affected by cancer dialysis conditions emulated with medium C in normoxia or hypoxia?

[0164] Growth on media A, B, and C As a first step, media A to C were prepared as described in Materials and Methods, and the ability of cancer cell lines to grow in these media was tested. Growth curves of selected cell lines over time in each medium were established. Cell numbers were analyzed after 1, 2 and 3 days of culture in media A to C under normoxia (21% O2).

[0165] As shown in Figure 10, reducing selected nutrients to more physiological levels in medium B significantly reduced the proliferation rate of the A549 lung cancer cell line and the RCC4 renal cancer cell line compared to medium A. Medium C further reduced the proliferation rate compared to medium A.

[0166] Growth of cancer cells in media A to C under normoxic and hypoxic conditions In Figure 11, cell mass after 3 days of culture in media A through C under normoxia and hypoxia is shown for the A549 lung cancer cell line and the RCC4 renal cancer cell line as well as primary renal carcinoma (RCC) cells. Again, proliferation rates in normoxia were reduced in media B and C compared to media A. The same pattern was seen for cells cultured at 5% O2. Again, for RCC4, low nutrient levels and the addition of BOHB to media C did not provide a significant additional effect compared to media B conditions.

[0167] For A549, a small but significant decrease in growth rate was observed between medium B and medium C, but only under normoxia.

[0168] Primary renal carcinoma cells from three patients were included in this study. Similar to the established cell lines, these cells showed reduced proliferation rates in media B and C compared to medium A.

[0169] Overall, changing the oxygen tension from 21% (normoxia) to 5% O2 (hypoxia) had very limited effect on the proliferation rate of these cells.

[0170] We then decided to include Acac in the study and to analyze the viability of cells cultured in the presence of BOHB and Acac alone or in combination with media A to C. Experiments were performed at 21% and 5% O2. Experiments were performed on the glioma cell lines A172 and U118MG.

[0171] BOHB is a chiral molecule and therefore exists in two enantiomers, D-BOHB and L-BOHB. D-BOHB is normally produced and metabolized in humans. The BOHB salt used in this study contained a 50:50 mixture of D-BOHB and L-BOHB. To ensure a high presence of the active D form, the total concentration of BOHB added was increased to 16 mM, giving a level of 8 mM D-BOHB. To keep the total concentration of active ketones constant, 8 mM Acac was used and for the combination of both ketones, the levels were adjusted to 4 mM Acac and 8 mM BOHB (containing 4 mM D-BOHB).

[0172] Acac available for in vitro use is in the form of a lithium salt. Because lithium itself can affect cancer cell viability [Cohen-Harazi et al., Anticancer Res 2020;40:3831-3837], 8 mM LiCl was used as a control for the 8 mM Acac data points and 4 mM LiCl was used as a control for the 4 mM Acac / 8 mM BOHB data.

[0173] At the end of the experiment, the culture medium from each well was collected and frozen to allow later measurement of lactate levels as a measure of metabolic status. In addition, duplicate experiments were performed in which one set of plates was frozen for later quantification of cell number using the CyQuant proliferation assay, and the amount of cells in the other set was analyzed with the CellTiterGlo viability assay.

[0174] Effects of adding BOHB and Acac alone or in combination As shown in Figures 12 and 13, initial experiments provided encouraging data regarding the effect of high ketone concentrations under nutrient-depleted conditions on the proliferation of A172 and U118MG glioma cell lines.

[0175] In medium A, addition of 16 mM BOHB alone had no growth inhibitory effect on A172 or U118MG cells under both normoxia and hypoxia, and 8 mM Acac did not further reduce cell number compared to the 8 mM LiCl control.

[0176] However, the addition of 4 mM Acac in combination with 8 mM BOHB significantly reduced the number of A172 cells in medium A under normoxia compared to the 4 mM LiCl control.

[0177] Interpretation of results from medium B was hampered by technical errors in normoxic control samples. However, in hypoxic A172 cells, BOHB significantly reduced cell number to approximately 70% of the amount in medium B without BOHB. A similar reduction was seen in hypoxic U118MG cells.

[0178] Furthermore, in medium B, 8 mM AcAc significantly reduced cell numbers compared to the 8 mM LiCl control in both cell lines, but only at 21% O2.

[0179] In medium C, the addition of 8 mM Acac alone did not significantly reduce cell mass compared to the 8 mM LiCl control, but for both cell lines and at both 21% and 5% O2, the addition of 16 mM BOHB significantly reduced cell numbers to approximately 30% compared to medium C without BOHB.

[0180] Additionally, the combination of BOHB and Acac significantly reduced cell numbers in medium C for both cell lines and at both oxygen levels compared to the 4 mM LiCl control.

[0181] These results suggest that the addition of high levels of BOHB or Acac alone does not inhibit the growth of glioma cells in a nutrient-rich environment such as medium A. Also, in medium B, at more physiological nutrient levels, only minor differences were seen when ketones were added. The greatest effect was seen in medium C, where both 16 mM BOHB alone and the combination of 8 mM BOHB and 4 mM Acac significantly reduced cell numbers compared to their respective controls in both hypoxic and normoxic conditions. This was not seen when 8 mM Acac was added alone.

[0182] However, repeating these experiments in normoxic conditions focusing on media B and C gave inconsistent results. Figures 14 to 16 show the combined results from experiments 2 to 6 for the glioma cell lines A172 and U118MG and the renal carcinoma cell line RCC4. Especially for the A172 cell line, there was a trend towards reduced proliferation in medium C when BOHB or Acac was added separately.

[0183] Results from Parts 1 and 2 of Example 2 showed that cancer cell lines grow more slowly in nutrient-limited environments. The cell lines tested appeared to survive in media B and C, although their growth rates were reduced. Optical inspection of the cells on day 3 showed no floating cells, which may be a sign of dead cells.

[0184] Data from the third part of the study show increased sensitivity of glioma cell lines to high levels of BOHB or the combination of BOHB and Acac in nutrient-limited Medium C. However, such sensitivity was not seen in the renal carcinoma cell line, RCC4.

Claims

1. 1. An extracorporeal blood treatment system (50) for treating a subject suffering from cancer, the system comprising: Extracorporeal blood circuit (52a, 52b); dialysate fluid circuit (54a, 54b); said extracorporeal blood circuit (52a, 52b) and a dialysate fluid circuit (54a, 54b) separated by a membrane (59) of a filtration unit (58); at least one blood pump (60) for controlling the flow of blood through said blood circuits (52a, 52b); at least one dialysate fluid pump (62, 68) for controlling the flow of dialysate fluid through said dialysate fluid circuit (54a, 54b); optionally, one or more infusion lines (66, 80, 81, 82), each infusion line adapted to be connected to said extracorporeal blood circuit (52a, 52b) or directly to the vascular system of the subject to be treated, each infusion line including an infusion pump; a system computing unit (64) operably connected to said blood pump (60) and said dialysate fluid pumps (62, 68) and optionally to said one or more infusion pumps of said one or more infusion lines (66, 80, 81, 82), said system computing unit including a user interface including input means and display means; Including, The system computing unit (64) determines a desired blood concentration value GLN of glutamine in the range of 0.1 to 0.5 mM. ｂ adapted to receive (901) The system computing unit (64) receives a desired blood concentration value GLUCOSE of glucose in the range of 2 to 4 mM. ｂ adapted to receive (903) The system computing unit (64) receives a desired blood concentration value KETONE of a ketone body, such as acetoacetate, β-hydroxybutyrate, or pharma- ceutically acceptable derivatives, esters, and salts thereof, in the range of 1 to 15 mM. ｂ adapted to receive (905) The system computing unit (64) receives a concentration value GLN representing the concentration of glutamine or a pharma- ceutically acceptable glutamine-containing compound in the new dialysate fluid. Ｐ adapted to receive (902) The system computing unit (64) receives a concentration value GLUCOSE, which represents the concentration of glucose in the new dialysate fluid. ｐ adapted to receive (904) Optionally, the system computing unit (64) may also generate a concentration value KETONE representing the concentration of ketone bodies, such as acetoacetate, β-hydroxybutyrate, or pharma- ceutically acceptable derivatives, esters and salts thereof, in the fresh dialysate fluid. ｐ adapted to receive (907) Optionally, the system computing unit (64) may also receive a concentration value KETONE representing the concentration of ketone bodies, such as acetoacetate, β-hydroxybutyrate or pharma- ceutically acceptable derivatives, esters and salts thereof, in an infusion fluid infused via one of the one or more infusion lines (66, 80, 81, 82) into the extracorporeal blood line (52b) or directly into the vascular system of the subject to be treated. ｉ adapted to receive (906) The system computing unit (64) receives the actual concentration value of glutamine in the blood from the treated subject, GLN ａ and receiving (909) an actual blood concentration value of glucose in blood GLUCOSE from the treated subject. ａ and receiving (910) an actual concentration value of ketone bodies, such as acetoacetate and / or β-hydroxybutyrate, KETONE ａ adapted to receive (911) The system computing unit (64) calculates the actual blood concentration value of glutamine GLN ａ GLN ｂ and the actual blood concentration value of glucose GLUCOSE ａ GLUCOSE ｂ adapted to control the blood pump (60) and the dialysate fluid pumps (62, 68) as described below (914); and If the system (50) comprises one or more of the infusion lines (66, 80, 81, 82), and if one of the infusion lines (66, 80, 81, 82) is adapted to infuse the infusate into the extracorporeal vascular line (52b) or directly into the vascular system of the subject being treated, the system computing unit (64) may further comprise a processor (100) for processing the actual blood concentration value KETONE. ａ KETONE ｂ adapted to control (920) the infusion pump of the infusion line such that Or, alternatively, If the system (50) does not include such an infusion line (66, 80, 81, 82), the system computing unit (64) ａ and KETONE ｂ and KETONE ａ <KETONE ｂ if so, displaying a message on the display informing the treated subject that he or she needs to consume an additional amount of ketone bodies or medium chain triglycerides.

2. The system (50) comprises one or more of the infusion lines (66, 80, 81, 82), and the system computing unit (64) receives a concentration value KETONE representing the concentration of ketone bodies, such as acetoacetate, β-hydroxybutyrate, or pharma- ceutically acceptable derivatives, esters and salts thereof, in an infusion fluid that is infused via one of the one or more infusion lines (66, 80, 81, 82) into the extracorporeal blood line (52b) or directly into the vascular system of the subject to be treated. ｉ and adapted to receive (906) The system computing unit (64) calculates the actual blood concentration value KETONE ａ KETONE ｂ 2. The extracorporeal blood treatment system of claim 1, adapted to control the infusion pump of the infusion line such that:

3. The system computing unit (64) ａ and actuating an associated infusion pump in one of said one or more infusion lines (66, 80, 81, 82), thereby ａ GLN ｂ If the GLN concentration is less than 100 mg / kg, an infusion of a composition containing glutamine or a pharma- ceutically acceptable glutamine-containing compound is initiated (916), and the GLN concentration is increased by 100 mg / kg. ａ GLN ｂ 3. The extracorporeal blood treatment system of claim 2, adapted to maintain the infusion until the infusion equals

4. The system computing unit (64) is ａ and actuating an associated infusion pump in one of said one or more infusion lines (66, 80, 81, 82), thereby ａ GLOCOSE ｂ If the glucose level is lower than 918, an infusion of a composition containing glucose is initiated (918), and the GLOCOSE ａ GLOCOSE ｂ 4. The extracorporeal blood treatment system (50) of claim 2 or 3, adapted to maintain said infusion until the infusion equals

5. 5. The system of claim 1, wherein the filtration membrane has a molecular weight cut-off (MWCO) of less than 60 kDa.

6. 6. The system of claim 5, wherein the filtration membrane has a MWCO of less than about 50 kDa, or less than about 40 kDa (such as less than 30 kDa, less than 10 kDa, less than 5 kDa, or less than 2 kDa).

7. 7. The system of claim 1, wherein the blood circuit comprises a thermal management system for heating or cooling blood in the blood line during use.

8. The system of claim 7 , wherein the thermal management system is controllable to regulate the temperature of the blood in the blood circuit to a temperature between 20° C. and 43° C.

9. The system further comprises one or more sensors (S, 90, 91, 92, 93) for detecting an analyte selected from the group of glucose, glutamine and ketone bodies, said sensors (S, 90, 91, 92, 93) preferably disposed in an outlet portion (54a) of said dialysate fluid circuit, said sensors being in communication with said system processing unit (64) to provide an output indicative of a concentration of said analyte in blood or, preferably, in spent dialysate fluid, said system processing unit (64) being configured to determine a representative blood concentration of an analyte from said outputs of said sensors (S, 90, 91, 92, 93), thereby determining a representative blood concentration of the analyte. ａ , GLUCOSE ａ , and KETONE ａ The system of claim 1 , further comprising:

10. A treatment set for use in an extracorporeal blood treatment system (50) according to any one of claims 1 to 9, said set comprising: a filtration unit (58) having a membrane (59) dividing an integrated blood line (52a, 52b) and an integrated dialysate fluid line (54a, 54b), said blood line (52a, 52b) and / or said dialysate fluid line (54a, 54b) being GLN ａ , GLUCOSE ａ , and KETONE ａ a treatment set including a sensor (S, 90, 91, 92, 93) for monitoring at least one of the above.

11. A method of treating a subject suffering from cancer using a system (50), the system (50) comprising: Extracorporeal blood circuit (52a, 52b); dialysate fluid circuit (54a, 54b); said extracorporeal blood circuit (52a, 52b) and a dialysate fluid circuit (54a, 54b) separated by a membrane (59) of a filtration unit (58); at least one blood pump (60) for controlling the flow of blood through said blood circuits (52a, 52b); At least one dialysate fluid pump (62, 68) for controlling the flow of dialysate fluid through said dialysate fluid circuit (54a, 54b); and optionally, one or more infusion lines (66, 80, 81, 82), each infusion line adapted to be connected to said extracorporeal circuit (52a, 52b) or directly to said vascular system of the subject to be treated, each infusion line including an infusion pump; The method comprises: A concentration value GLN representing a desired blood concentration of glutamine in the range of 0.1 to 0.5 mM. ｂ receiving (901); A concentration value GLUCOSE representing a desired blood concentration of glucose in the range of 2 to 4 mM. ｂ receiving (903); A concentration value KETONE representing a desired blood concentration of a ketone body, such as acetoacetate, β-hydroxybutyrate, or pharma- ceutically acceptable derivatives, esters, and salts thereof, in the range of 1 to 15 mM. ｂ receiving (905); a concentration value GLN representing the concentration of glutamine, or a pharma- ceutically acceptable glutamine-containing compound, in the new dialysate fluid; ｐ receiving (902); A concentration value GLUCOSE representing the concentration of glucose in the new dialysate fluid. ｐ receiving (904); Optionally, a concentration value KETONE representing the concentration of ketone bodies, such as acetoacetate, β-hydroxybutyrate, or pharma- ceutically acceptable derivatives, esters, and salts thereof, in the fresh dialysate fluid. ｐ receiving (907); Optionally, a concentration value KETONE representing the concentration of ketone bodies, such as acetoacetate, β-hydroxybutyrate, or pharma- ceutically acceptable derivatives, esters, and salts thereof, in an infusion solution infused into the extracorporeal blood line (52b) or directly into the vascular system of the subject to be treated via one of the one or more infusion lines (66, 80, 81, 82). ｉ receiving (906); a concentration value GLN representing the actual concentration of glutamine in the blood of the treated subject; ａ receiving (909); A concentration value GLUCOSE representing the actual glucose concentration in the blood of the treated subject ａ receiving (910); A concentration value KETONE that represents the actual concentration of ketone bodies such as acetoacetate and / or β-hydroxybutyrate ａ receiving (911); The blood pump (60) and the at least one dialysate fluid pump (62, 68) are controlled to obtain the actual concentration value GLN of glutamine. ａ GLN ｂ and the actual concentration value of glucose GLUCOSE ａ GLUCOSE ｂ To be done (914) as follows: and When the system (50) comprises one or more of the infusion lines (66, 80, 81, 82), one of the infusion lines (66, 80, 81, 82) injects the infusate into the extracorporeal blood line (52b) or directly into the vascular system of the subject being treated, KETON ａ KETON ｂ controlling the injection so that (920) Or, alternatively, If the system 50 does not infuse an infusion solution containing ketone bodies, the subject being treated will ａ KETON ｂ and if the blood sugar level is lower than 100 mg / kg, the patient is asked to orally ingest an amount of ketone bodies or medium chain triglycerides.

12. The system (50) includes one or more of the infusion lines (66, 80, 81, 82), and the method comprises: A concentration value KETONE representing the concentration of ketone bodies, such as acetoacetate, β-hydroxybutyrate, or pharma- ceutically acceptable derivatives, esters, and salts thereof, in the infusion solution. ｉ receiving (906); injecting the infusion solution through one of the one or more infusion lines (66, 80, 81, 82) into the extracorporeal blood line (52b) or directly into the vascular system of the subject to be treated; and The actual blood concentration value KETONE ａ KETONE ｂ 12. The method of claim 11, further comprising controlling (920) the infusion pump of the infusion line such that:

13. 13. The method of claim 11 or 12, wherein the cancer is selected from human colon cancer and glioblastoma, as well as prostate cancer, breast cancer and liver cancer.

14. 1. A system computing unit (64) adapted to control an extracorporeal blood treatment system (50) for treating a subject suffering from cancer, said system computing unit comprising: a plurality of output means adapted to be operatively connected to at least one blood pump (60), at least one dialysate fluid pump (62, 68), and optionally one or more infusion pumps for controlling the flow of each of the one or more infusion lines (66, 80, 81, 82); A user interface including an input means and a display means; and storage means and computing means; The system computing unit (64) determines the desired blood concentration value of glutamine, GLN ｂ adapted to receive (901) The system computing unit (64) determines the desired blood concentration value of glucose GLUCOSE ｂ adapted to receive (903) The system computing unit (64) determines the desired blood concentration value of ketone bodies, KETONE ｂ adapted to receive (905) The system computing unit (64) calculates the dialysate concentration value of glutamine GLN ｐ adapted to receive (902) The system computing unit (64) calculates the glucose dialysate concentration value GLUCOSE ｐ adapted to receive (904) Optionally, the system computing unit (64) may also calculate a concentration value KETONE representing the concentration of ketone bodies, such as acetoacetate, β-hydroxybutyrate, or pharma- ceutically acceptable derivatives, esters and salts thereof, in the fresh dialysate. ｐ adapted to receive (907) Optionally, the system computing unit (64) may also calculate a ketone body infusate concentration value KETONE ｉ adapted to receive (906) The system computing unit (64) calculates the actual blood concentration value of glutamine GLN ａ adapted to receive (909) The system computing unit (64) receives the actual blood glucose concentration value GLUCOSE ａ adapted to receive (910) The system computing unit (64) may receive actual blood concentration values ​​of ketone bodies, such as β-hydroxybutyrate and / or acetoacetate, KETONE ａ adapted to receive (911) The system computing unit (64) controls the blood pump (60) and the dialysate fluid pumps (62, 68) to calculate the actual blood concentration value of glutamine GLN ａ GLN ｂ and the actual blood concentration value of glucose GLUCOSE ａ Glucose ｂ 9. The method according to claim 9, and If an infusion pump is operatively connected to the system computing unit (64), the system computing unit (64) controls the infusion pump to calculate the actual blood concentration value KETONE. ａ KETONE ｂ and adapted to be (920) and If an infusion pump is not operatively connected to the system computing unit (64), the system computing unit (64) ａ and KETONE ｂ and KETONE ａ <KETONE ｂ and a system computing unit adapted to display a message on the display informing the treated subject that the treated subject needs to consume an additional amount of ketone bodies or medium chain triglycerides if

15. A dialysate fluid suitable for dialysis treatment of cancer, comprising a ketone body such as acetoacetate, beta-hydroxybutyrate, or pharma-ceutically acceptable derivatives, esters and salts thereof.

16. a) glutamine or a glutamine-containing compound, and b) Glucose 16. The dialysate fluid of claim 15, further comprising at least one of:

17. a) the concentration of glutamine or glutamine-containing compound is in an amount of 0 to 0.5 mM, preferably 0.05 to 0.3 mM; b) the concentration of glucose is in an amount of 0 to 6 mM, preferably 0.5 to 4 mM; 16. The dialysis fluid according to claim 15, wherein c) the concentration of ketone bodies is in an amount of 1 to 15 mM, preferably 2 to 12 mM.

Images