Monitoring and Management of Cell Therapy-Induced Toxicity

Abstract

The present disclosure generally relates to compositions and methods for identifying cell therapy patients who are likely or unlikely to experience toxicity following cell therapy. The methods are based on the discovery that pre-treatment covariates such as serum IL-15 and MCP-1 levels in the patient, or viability of the cells being administered, can be used to predict the likelihood of developing such toxicity. Once a patient is identified as likely or unlikely to experience toxicity, compositions and methods for monitoring and managing toxicity are also provided.

Description

[Technical Field]

[0001] (CROSS-REFERENCE TO RELATED APPLICATIONS) This application claims priority to U.S. Provisional Patent Application No. 63 / 227,677, filed July 30, 2021, and U.S. Provisional Patent Application No. 63 / 279,615, filed November 15, 2021, the entire contents of each of which are incorporated herein by reference.

[0002] FIELD OF THE INVENTION The present disclosure relates to methods for determining whether a patient is likely or unlikely to experience toxicity following cell therapy treatment. [Background technology]

[0003] Chimeric antigen receptor T cells (also known as CAR T cells) are T cells genetically engineered to produce an artificial T cell receptor for use in immunotherapy. CAR-T therapy has the potential to improve the management of lymphomas and possibly solid tumors. Two anti-CD19 CAR T cell products, axicabtagene ciloleucel (axi-cel) and tisagenlecleucel, have been approved for the management of relapsed / refractory large B-cell lymphoma.

[0004] However, CAR-T therapy is associated with two common toxicities, cytokine release syndrome (CRS) and immune effector cell-associated neurotoxicity syndrome (ICANS), which are typically observed acutely after therapy. In addition, delayed toxicities include prolonged cytopenias and on-target off-tumor effects.

[0005] CRS is a systemic inflammatory response triggered by the release of cytokines following activation of CAR-T cells in response to tumor recognition. CAR-T cells also activate bystander immune cells, such as macrophages, which then release proinflammatory cytokines, likely contributing to the pathophysiology of CRS. CRS typically occurs with symptoms of fever, muscle pain, stiffness, fatigue, and loss of appetite. CRS can also lead to multiple organ dysfunction.

[0006] ICANS can occur during CRS or, more commonly, after CRS has subsided. ICANS typically manifests as toxic encephalopathy with word-finding difficulties, aphasia, and confusion, but in more severe cases can progress to decreased level of consciousness, coma, seizures, motor paralysis, and cerebral edema. Cytokines, chemokines, and the degree of CAR-T cell proliferation are associated with the severity of neurotoxicity.

[0007] Monitoring for CRS and neurotoxicity is required for patients receiving CAR-T infusions. Given the potential severity of toxicity, such monitoring must be performed daily for seven days at a certified medical facility. In addition, patients are instructed to remain near a certified medical facility for at least four weeks after the infusion. Such monitoring incurs significant costs.

[0008] There is a strong need for methods to predict the onset of such toxicity so that only those who require toxicity treatment need remain in the facility, which could help reduce unnecessary hospitalizations, and those predicted to be more likely to experience toxicity can receive appropriate treatment or prevention for toxicity. Summary of the Invention

[0009] The present disclosure provides compositions and methods for identifying cell therapy patients who are likely or unlikely to experience toxicity after cell therapy. The methods are based on the discovery that pre-treatment covariates, such as serum IL-15 and MCP-1 levels in the patient, or the viability of the administered cells, can be used to predict the likelihood of developing such toxicity. Once a patient has been identified as likely or unlikely to experience toxicity, compositions and methods for monitoring and managing toxicity are also provided.

[0010] One embodiment provides a method for identifying a patient as likely or unlikely to experience toxicity after cell therapy, comprising measuring a level of IL-15 (Interleukin-15) or MCP-1 (monocyte chemoattractant protein-1) in a blood sample from the patient, and identifying the patient as likely to experience toxicity after cell therapy if the IL-15 or MCP-1 level is higher than a corresponding reference level, or identifying the patient as not likely to experience toxicity after cell therapy if the IL-15 or MCP-1 level is lower than the corresponding reference level, wherein the cell therapy comprises administration of immune cells.

[0011] In some embodiments, the immune cells comprise T cells. In some embodiments, the T cells are engineered to express a chimeric antigen receptor (CAR). In some embodiments, the CAR has binding specificity for the CD19 (cluster of differentiation 19) protein. In some embodiments, the cell therapy comprises axicabtagenecilloreucel.

[0012] In some embodiments, the blood sample is a serum sample. In some embodiments, the blood sample is obtained from the patient prior to cell therapy. In some embodiments, the blood sample is obtained after the patient has undergone a preconditioning treatment. In some embodiments, the preconditioning treatment reduces lymphocytes in the patient. In some embodiments, the preconditioning comprises intravenous (iv) administration of cyclophosphamide and fludarabine given 5, 4, and / or 3 days prior to cell therapy.

[0013] In some embodiments, the toxicity is selected from the group consisting of cytokine release syndrome (CRS), a neurologic event (NE), and combinations thereof. In some embodiments, the toxicity is early-onset toxicity. In some embodiments, the early-onset toxicity occurs within 4 days after cell therapy.

[0014] In some embodiments, the reference levels for IL-15 or MCP-1 are determined from patients who experience toxicity after cell therapy and patients who do not experience toxicity after cell therapy.

[0015] In some embodiments, the method further comprises measuring the viability of cells used in the cell therapy, and if the IL-15 or MCP-1 levels are higher than the corresponding reference levels and the cell viability is higher than the reference cell viability, the patient is identified as likely to experience toxicity after the cell therapy, or if the IL-15 or MCP-1 levels are lower than the corresponding reference levels and the cell viability is lower than the reference cell viability, the patient is identified as not likely to experience toxicity after the cell therapy.

[0016] In some embodiments, a patient is identified as likely to experience toxicity after cell therapy if the IL-15 and MCP-1 levels are higher than the corresponding reference levels and the cell viability is higher than the reference cell viability, or a patient is identified as not likely to experience toxicity after cell therapy if the IL-15 and MCP-1 levels are lower than the corresponding reference levels and the cell viability is lower than the reference cell viability.

[0017] In some embodiments, the method further comprises obtaining one or more of the patient's baseline hemoglobin, baseline tumor burden, baseline LDH, baseline creatinine, and baseline calcium levels.

[0018] In some embodiments, the method further comprises monitoring the patient for toxicity at a medical care facility if the patient is identified as likely to experience toxicity.

[0019] In some embodiments, the method further comprises preventing or treating toxicity in the patient if the patient is identified as likely to experience toxicity. In some embodiments, the treating or preventing comprises administering an agent selected from the group consisting of an antihistamine, a corticosteroid, an antihypotensive, an IL-6 inhibitor, a GM-CSF inhibitor, and a nonsteroidal anti-inflammatory drug. In some embodiments, the treating or preventing comprises administering an agent selected from the group consisting of tocilizumab, dexamethasone, levetiracetam, lenzilumab, methylprednisolone, anakinra, siltuximab, ruxolitinib, cyclophosphamide, IVIG (intravenous immunoglobulin), and ATG (antithymocyte globulin).

[0020] In some embodiments, the method further comprises releasing the patient from the medical care facility after no more than two days in the medical care facility if the patient is identified as not likely to experience toxicity.

[0021] Also provided in one embodiment is a kit or package useful for identifying patients likely to experience toxicity following cell therapy, the kit or package comprising polynucleotide primers or probes or antibodies for measuring expression levels of IL-15 and MCP-1 in a biological sample.

[0022] Also provided in one embodiment is a method for preventing or treating toxicity in a patient undergoing cell therapy, comprising administering to the patient an agent that prevents or treats cytokine release syndrome (CRS) or a neurological event (NE), wherein the patient has been identified as likely to experience toxicity following cell therapy based on a level of IL-15 (interleukin-15) or MCP-1 (monocyte chemotactic protein-1) in a blood sample from the patient being higher than a corresponding reference level.

[0023] In some embodiments, the agent is selected from the group consisting of an antihistamine, a corticosteroid, an antihypotensive, an IL-6 inhibitor, a GM-CSF inhibitor, and a nonsteroidal anti-inflammatory drug. In some embodiments, the agent is selected from the group consisting of tocilizumab, dexamethasone, levetiracetam, lenzilumab, methylprednisolone, anakinra, siltuximab, ruxolitinib, cyclophosphamide, IVIG (intravenous immunoglobulin), and ATG (antithymocyte globulin).

[0024] Also provided in one embodiment is a computer program product for use with a computer system, the computer program product including a computer-readable storage medium and a computer program mechanism embedded therein, the computer mechanism including executable instructions for performing a method for identifying a patient as likely to experience toxicity following cell therapy, the instructions including: (i) obtaining a level of IL-15 (interleukin-15) or MCP-1 (monocyte chemoattractant protein-1) in a blood sample from the patient; and (ii) comparing the level to a corresponding reference level, wherein the patient is identified as likely to experience toxicity following cell therapy if the IL-15 or MCP-1 level is higher than the corresponding reference level, and the cell therapy includes administration of immune cells. [Brief explanation of the drawings]

[0025] [Figure 1] Indicates the patient's condition in definition C.

[0026] [Figure 2] Figure 1 shows the ROC of BPM with cell viability + IL-15 + MCP-1 for outpatient A3, where BPM is RFCRUS and the optimal cutoff is 0.538.

[0027] [Figure 3] Boxplot of predictions for training data, BPM, with cell viability + IL-15 + MCP-1 for outpatient A3.

[0028] [Figure 4] Figure 1 shows the box plot of the predicted for BPM, study data with cell viability + IL-15 + MCP-1 for outpatient A3.

[0029] [Figure 5]1 shows the decision tree for Cell Viability + IL-15 + MCP-1 for training data with outpatient A3, where subjects on leaves with an "N" are classified as "inpatients" and subjects on leaves with a "Y" are classified as "outpatients."

[0030] [Figure 6] 1 shows the decision tree for Cell Viability + IL-15 + MCP-1 for study data with outpatient A3, where subjects on leaves with an "N" are classified as "inpatients" and subjects on leaves with a "Y" are classified as "outpatients."

[0031] [Figure 7] 1 shows partial dependence plots (based on balanced RFs) showing that higher cell viability, IL-15, and MCP-1 are associated with a higher likelihood of early toxicity.

[0032] [Figure 8] FIG. 1 is a schematic diagram illustrating computing components that may be used to implement various features of the embodiments described in this disclosure. DETAILED DESCRIPTION OF THE INVENTION

[0033] definition

[0034] The following description describes exemplary embodiments of the present technology, however, it should be recognized that such description is not intended to limit the scope of the present disclosure, but is instead provided as a description of exemplary embodiments. definition

[0035] As used herein, the following words, phrases, and symbols are generally intended to have the meanings set forth below, unless the context in which they are used indicates otherwise.

[0036] As used herein, certain terms may have the following defined meanings: As used in this specification and claims, the singular forms "a," "an," and "the" include singular and plural references unless the context clearly dictates otherwise. For example, the term "a cell" includes a single cell as well as a plurality of cells, including mixtures thereof.

[0037] All numerical designations, e.g., pH, temperature, time, concentration, and molecular weight, including ranges, are approximations that are varied (+) or (-) in increments of 0.1. It is understood, although not always explicitly stated, that all numerical designations are preceded by the term "about." The term "about" includes the exact value "X" as well as fractional increments of "X," such as "X+0.1" or "X-0.1." It is also understood, although not always explicitly stated, that the reagents described herein are exemplary only, and that equivalents of such are known in the art.

[0038] The term "immunotherapy" refers to the treatment of a subject suffering from a disease or at risk of suffering from or experiencing a recurrence of a disease by methods that involve inducing, enhancing, suppressing, or otherwise modifying an immune response. Examples of immunotherapy include, but are not limited to, T cell therapy. T cell therapy can include adoptive T cell therapy, tumor-infiltrating lymphocyte (TIL) immunotherapy, autologous cell therapy, engineered autologous cell therapy (eACT™), and allogeneic T cell transplantation. However, one skilled in the art will recognize that the conditioning methods disclosed herein enhance the effectiveness of any transplanted T cell therapy. Examples of T cell therapy are described in U.S. Patent Application Publication Nos. 2014 / 0154228 and 2002 / 0006409, U.S. Patent No. 7,741,465, U.S. Patent No. 6,319,494, U.S. Patent No. 5,728,388, and WO 2008 / 081035. In some embodiments, the immunotherapy comprises CAR T cell therapy. In some embodiments, the CAR T cell therapy product is administered via infusion.

[0039] T cells for immunotherapy can be derived from any source known in the art. For example, T cells can be differentiated in vitro from a hematopoietic stem cell population, or T cells can be obtained from a subject. T cells can be obtained, for example, from peripheral blood mononuclear cells (PBMCs), bone marrow, lymph node tissue, umbilical cord blood, thymus tissue, tissue from an infection site, ascites, pleural effusion, spleen tissue, and tumors. In addition, T cells can be derived from one or more T cell lines available in the art. T cells can also be obtained from a unit of blood drawn from a subject using various techniques known to those skilled in the art, such as FICOLL™ separation and / or apheresis. Additional methods for isolating T cells for T cell therapy are disclosed in U.S. Patent Application Publication No. 2013 / 0287748, which is incorporated herein by reference in its entirety.

[0040] As used herein, "cytokine" refers to a non-antibody protein released by one cell in response to contact with a specific antigen, where the cytokine interacts with a second cell and mediates a response in the second cell. As used herein, "cytokine" refers to a protein released by one cell population that acts on another cell as an intercellular mediator. Cytokines can be endogenously expressed by cells or administered to a subject. Cytokines can be released by immune cells, including macrophages, B cells, T cells, and mast cells, to propagate an immune response. Cytokines can induce various responses in recipient cells. Cytokines can include homeostatic cytokines, chemokines, proinflammatory cytokines, effectors, and acute phase proteins. For example, homeostatic cytokines, including interleukin (IL) 7 and IL-15, can promote immune cell survival and proliferation, and proinflammatory cytokines can promote an inflammatory response. Examples of homeostatic cytokines include, but are not limited to, IL-2, IL-4, IL-5, IL-7, IL-10, IL-12p40, IL-12p70, IL-15, and interferon (IFN) gamma.Examples of proinflammatory cytokines include, but are not limited to, IL-1a, IL-1b, IL-6, IL-13, IL-17a, tumor necrosis factor (TNF)-alpha, TNF-beta, fibroblast growth factor (FGF)2, granulocyte macrophage colony-stimulating factor (GM-CSF), soluble intercellular adhesion molecule 1 (sICAM-1), soluble vascular adhesion molecule 1 (sVCAM-1), vascular endothelial growth factor (VEGF), VEGF-C, VEGF-D, and placental growth factor (PLGF). Examples of effectors include, but are not limited to, granzyme A, granzyme B, soluble Fas ligand (sFasL), and perforin. Examples of acute phase proteins include, but are not limited to, C-reactive protein (CRP) and serum amyloid A (SAA).

[0041] A "chemokine" is a type of cytokine that mediates chemotaxis or directional movement of cells. Examples of chemokines include, but are not limited to, IL-8, IL-16, eotaxin, eotaxin-3, macrophage-derived chemokine (MDC or CCL22), monocyte chemotactic protein 1 (MCP-1 or CCL2), MCP-4, macrophage inflammatory protein 1α (MIP-1α, MIP-1a), MIP-1β (MIP-1b), gamma-inducible protein 10 (IP-10), and thymus and activation-regulated chemokine (TARC or CCL17).

[0042] The terms "genetically engineered" or "engineered" refer to methods of modifying the genome of a cell, such as, but not limited to, deleting a coding or non-coding region or portion thereof, or inserting a coding region or portion thereof. In some embodiments, the cell being modified is a lymphocyte, e.g., a T cell, which can be obtained from either a patient or a donor. The cell can be modified to express an exogenous construct, such as, for example, a chimeric antigen receptor (CAR) or a T cell receptor (TCR), where the exogenous construct is integrated into the genome of the cell.

[0043] As used herein, a "patient" includes any human suffering from cancer (e.g., lymphoma or leukemia). The terms "subject" and "patient" are used interchangeably herein.

[0044] The terms "reduce" and "decrease" are used interchangeably herein and refer to any change below the original. "Reduce" and "decrease" are relative terms and require a comparison between before and after measurement. "Reduce" and "decrease" include complete depletion. Similarly, the term "increase" refers to any change above the original value. "Increase," "higher," and "lower" are relative terms and require a comparison between before and after measurement and / or a comparison between reference standards. In some embodiments, the reference value is obtained from the general population, which may be the general population of patients. In some embodiments, the reference value is derived from a quartile analysis of the general patient population.

[0045] "Treatment" or "treating" a subject refers to any type of intervention or process performed on a subject, or the administration of an active agent to a subject, with the intent of reversing, alleviating, ameliorating, inhibiting, delaying, or preventing the onset, progression, occurrence, severity, or recurrence of a symptom, complication, or condition, or biochemical manifestations associated with a disease. In some embodiments, "treatment" or "treating" encompasses partial remission. In other embodiments, "treatment" or "treating" includes complete remission.

[0046] The present disclosure further provides diagnostic, prognostic, and therapeutic methods based at least in part on determining the expression levels of the genes of interest identified herein.

[0047] For example, information obtained using the diagnostic assays described herein is useful in determining whether a subject is likely to suffer from or develop a disease (e.g., cytokine release syndrome), or whether they are suitable for treatment. Based on the diagnostic / prognostic information, a physician can recommend a treatment protocol.

[0048] As used throughout, the term "likely" refers to a higher probability of occurrence than a higher probability of not occurring, alternatively, a higher probability of occurrence relative to a given average control. As a non-limiting example, a patient who is likely to experience toxicity after cell therapy refers to a patient who has a higher probability of experiencing toxicity than a patient who does not experience toxicity. Alternatively, a patient who is likely to experience toxicity after cell therapy refers to a patient who has a higher statistical chance of experiencing toxicity compared to the average occurrence of toxicity in a patient population treated with cell therapy. Those skilled in the art will recognize additional definitions in addition to those set forth above.

[0049] It will be understood that the information obtained using the diagnostic assays described herein can be used alone or in combination with other information, including, but not limited to, behavioral assessments, genotypes or expression levels of other genes, clinical chemistry parameters, histopathological parameters, or the age, sex, and weight of the subject. Prediction and management of early-onset acute toxicity

[0050] For cancer patients receiving current CAR-T therapy, daily monitoring for signs and symptoms of CRS and neurotoxicity at an accredited medical center after CAR-T infusion is required. Patients with grade 3 or higher cytokine release syndrome (CRS) and neurologic events (NE) require intensive inpatient management.

[0051] Using machine learning techniques, the present disclosure describes compositions and methods for predicting early-onset acute toxicity in patients receiving CAR-T therapy. Based on such predictions, the present disclosure also provides methods for preventing and, if necessary, treating toxicity in patients at risk of experiencing toxicity.

[0052] As demonstrated in the Examples, multivariate analysis and machine learning from data obtained from evaluable patients in patients participating in clinical trials for CAR-T therapy yielded several comparable predictive models for early-onset CRS or NE, with the best-performing models having a receiver operating characteristic (ROC) AUC (area under the ROC curve) greater than 0.8 in training and greater than 0.7 in testing.

[0053] When used alone, each of these covariates independently correlated with the likelihood of developing toxicity. Collectively, the predictive power is further increased. Exemplary covariates include, but are not limited to, product cell viability (or simply cell viability), serum IL-15 levels on day 0 before infusion, and serum MCP-1 (CCL2) levels on day 0 before infusion. Additional exemplary covariates include hemoglobin levels, albumin levels, red blood cell count, and ferritin levels (on day 0 before infusion); blood concentrations (levels) of urate, calcium, phosphate, creatinine, chloride, LDH (lactate dehydrogenase), and IL-17 (baseline); and red blood cell count, white blood cell count, neutrophil count, and basophil count (baseline).

[0054] According to one embodiment of the present disclosure, a method is provided for identifying a patient as likely to experience toxicity after cell therapy. In some embodiments, the method involves measuring the level of IL-15 (interleukin-15) in a patient sample. It has been discovered herein that a higher level of IL-15 correlates with a higher incidence of toxicity after cell therapy. Thus, the method further involves identifying the patient as likely to experience toxicity after cell therapy if the IL-15 level is higher than a reference level (or cutoff level).

[0055] According to one embodiment of the present disclosure, a method is provided for identifying a patient as likely to experience toxicity after cell therapy. In some embodiments, the method involves measuring the level of MCP-1 (monocyte chemoattractant protein-1) in a patient sample. It has been discovered herein that a higher level of MCP-1 correlates with a higher incidence of toxicity after cell therapy. Accordingly, the method further involves identifying a patient as likely to experience toxicity after cell therapy if the IL-15 level is higher than a reference level (or cutoff level).

[0056] According to one embodiment of the present disclosure, a method for identifying a patient as likely to experience toxicity after cell therapy is provided. In some embodiments, the method involves measuring cell viability. It has been discovered herein that a higher viability of infused cells correlates with a higher incidence of toxicity after cell therapy. Thus, the method further involves identifying a patient as likely to experience toxicity after cell therapy if the cell viability is higher than a reference level (or cutoff level).

[0057] In some embodiments, measurements useful for predicting the onset of toxicity are any one or more of the following: blood hemoglobin levels, albumin levels, red blood cell count, and ferritin levels (day 0 pre-infusion); blood concentrations (levels) of urate, calcium, phosphate, creatinine, chloride, LDH (lactate dehydrogenase), and IL-17 (baseline); and covariates of red blood cell count, white blood cell count, neutrophil count, and basophil count (baseline).

[0058] In some embodiments, the blood covariate (e.g., IL-15) is measured in a blood sample obtained from the patient, which in some embodiments is a serum sample.

[0059] In some embodiments, blood samples are obtained from patients at designated time points. For example, for baseline covariates, blood samples are drawn before cell therapy begins. For day 0 covariates, blood samples are drawn on day 0, the day the infusion is administered. In some embodiments, blood samples are drawn before the infusion.

[0060] In some embodiments, the patient receives a preconditioning treatment prior to cell therapy, and thus day 0 is after the preconditioning treatment. In some embodiments, the preconditioning is leukocyte-depleting or lymphocyte-depleting. An exemplary lymphocyte-depleting regimen is intravenous cyclophosphamide 500 mg / m 2 and fludarabine 30 mg / m 2 and two other treatments, both given on days 5, 4, and 3 prior to the start of CAR-T infusion.

[0061] Reference levels (cutoff values) for any of the above-mentioned covariates, IL-15 level, MCP-1 level, and cell viability, can be determined experimentally or from historical data using methods known in the art. The reference level for each corresponding covariate can be determined before or after measurement. In some embodiments, the reference level best separates (distinguishes) patients with different toxicity outcomes after the same cell therapy.

[0062] In some embodiments, the reference level is a specific number, such as 0.1 ng / mL. However, in some embodiments, the reference level is implicit in multiple reference standards. For example, a measured level can be compared to the number of multiple reference numbers, each labeled toxic or non-toxic, using a nearest neighbor method. If the measured level is closer to the reference level associated with a patient experiencing toxicity, the measured level predicts that the patient is likely to experience toxicity as well. In this example, a specific reference level is not derived from the reference number, but a comparison is effectively made.

[0063] In some embodiments, the reference level is implicit in the formula used to calculate the probability based on the measured level. For example, a linear or quadratic discriminant analysis formula can be developed based on training data and used to determine a probability number taking the measured level as input.

[0064] In some embodiments, covariates can be used in combination. For example, a patient is identified as likely to experience toxicity after cell therapy when both IL-15 and MCP-1 levels are higher than their corresponding reference levels. In some embodiments, a patient is identified as likely to experience toxicity after cell therapy when both IL-15 and cell viability are higher than their corresponding reference levels. In some embodiments, a patient is identified as likely to experience toxicity after cell therapy when both MCP-1 and cell viability are higher than their corresponding reference levels. In some embodiments, a patient is identified as likely to experience toxicity after cell therapy when IL-15, MCP-1, and cell viability are all higher than their corresponding reference levels. In some embodiments, one or more additional covariates are also included.

[0065] In some embodiments, the reference level (plasma concentration) for IL-15 is 20pg / mL, 21pg / mL, 22pg / mL, 23pg / mL, 24pg / mL, 25pg / mL, 26pg / mL, 27pg / mL, 28pg / mL, 29pg / mL, 30pg / mL, 31pg / mL, 32pg / mL, 33pg / mL, 34pg / mL, 35pg / mL, 36pg / mL, 37pg / mL, 38pg / mL, 39pg / mL, 40pg / mL, 41pg / mL, 42pg / mL, 43pg / mL, 44pg / mL, 45pg / mL, 46pg / mL, 47pg / mL, 48pg / mL, 49pg / mL, or 50pg / mL. In an exemplary embodiment, the reference level for IL-15 is 28 pg / mL.

[0066] In some embodiments, the reference levels (plasma concentrations) for CCL2 are 600pg / mL, 620pg / mL, 640pg / mL, 650pg / mL, 660pg / mL, 680pg / mL, 700pg / mL, 720pg / mL, 740pg / mL, 750pg / mL, 760pg / mL, 780pg / mL, 800pg / mL, 820pg / mL, 840pg / mL, 850pg / mL, 860pg / mL, 880pg / mL, 900pg / mL, 920pg / mL, 940pg / mL, 950pg / mL, 960pg / mL, 980pg / mL, 1000pg / mL, 1020pg / mL, 1040pg / mL, 1060pg / mL, 1080pg / mL, 1100pg / mL, 1120pg / mL, 1140pg / mL, 1160pg / mL, 1180pg / mL, 1180pg / mL, 1190pg / mL, 1200pg / mL, 1220pg / mL, 1240pg / mL, 1260pg / mL, 1280pg / mL, 1280pg / mL, 1300pg / mL, 1320pg / mL, 1340pg / mL, 1360pg / mL, 1380pg / mL, 1360pg / mL, 1380pg / mL, 1400pg / mL, 1400pg / mL, 1420pg / mL, 1040pg / mL, 1050pg / mL, 1060pg / mL, 1080pg / mL, 1100pg / mL, 1120pg / mL, 1140 pg / mL, 1150pg / mL, 1160pg / mL, 1180pg / mL, 1200pg / mL, 1220pg / mL, 1240pg / mL, 1 250pg / mL, 1260pg / mL, 1280pg / mL, 1300pg / mL, 1320pg / mL, 1340pg / mL, 1350pg / m L, 1360pg / mL, 1380pg / mL, 1400pg / mL, 1420pg / mL, 1440pg / mL, or 1450pg / mL.

[0067] In some embodiments, the reference level for product cell viability is 93%, 93.5%, 94%, 94.5%, 95%, 95.5%, 96%, 96.5%, or 97%. In an exemplary embodiment, the reference level for product cell viability is 95%.

[0068] In some embodiments, the cell therapy is a therapy involving the administration of immune cells, which may be, but are not limited to, T cells, natural killer (NK) cells, monocytes, or macrophages.

[0069] In some embodiments, immune cells are engineered to express chimeric antigen receptors (CARs), resulting in the production of, but not limited to, CAR-T cells, CAR-NK cells, etc. In some embodiments, the CAR has binding specificity for a tumor antigen.

[0070] A "tumor antigen" is an antigenic substance produced in tumor cells, i.e., it provokes an immune response in the host. Tumor antigens are useful for identifying tumor cells and are potential candidates for use in cancer therapy. Normal proteins in the body are not antigenic. However, certain proteins are produced or overexpressed during tumor formation and therefore appear to be "foreign" to the body. This may include normal proteins that are well isolated from the immune system, proteins that are normally produced in very small amounts, proteins that are normally produced only at certain developmental stages, or proteins whose structure has been altered by mutation.

[0071] Numerous tumor antigens are known in the art, and new tumor antigens can be readily identified by screening. Non-limiting examples of tumor antigens include EGFR, Her2, EpCAM, CD19, CD20, CD30, CD33, CD47, CD52, CD133, CD73, CEA, gpA33, mucin, TAG-72, CIX, PSMA, folate binding protein, GD2, GD3, GM2, VEGF, VEGFR, integrin, αVβ3, α5β1, ERBB2, ERBB3, MET, IGF1R, EPHA3, TRAILR1, TRAILR2, RANKL, FAP, and tenascin.

[0072] In some embodiments, the CAR has specificity for any of the tumor antigens discussed above, or for any one or more of CD19, CD20, CLL-1, TACI, MAGE, HPV-associated protein, GPC-3, and BCMA. In some embodiments, the CAR has bispecificity for two or more antigens (e.g., CD19 and CD20).

[0073] In some embodiments, the CAR has specificity for CD19 (cluster of differentiation 19). An exemplary cell therapy targeting CD19 is axicabtagene ciloreucel. Axicabtagene ciloreucel, sold under the trade name Yescarta®, is a treatment for large B-cell lymphoma that has failed conventional therapies.

[0074] In some embodiments, the toxicity is selected from the group consisting of cytokine release syndrome (CRS), neurological events (NE), and combinations thereof. In some embodiments, the toxicity is early-onset toxicity. In some embodiments, early-onset toxicity occurs within 5 days, 4 days, 3 days, or 2 days after cell therapy.

[0075] Key symptoms of CRS include fever, hypotension, tachycardia, hypoxia, chills, and headache. Serious events that may be associated with CRS include cardiac arrhythmias (including atrial fibrillation and ventricular tachycardia), cardiac arrest, heart failure, renal failure, capillary leak syndrome, hypotension, hypoxia, multiple organ failure, and hemophagocytic lymphohistiocytosis / macrophage activation syndrome (MAS). CRS can be classified into four different grades: grades 1 to 4.

[0076] The most common neurotoxicities include encephalopathy, headache, tremors, dizziness, delirium, aphasia, and insomnia. Serious events include leukoencephalopathy and seizures. Neurotoxicity can be classified into four different grades, grades 1 to 4.

[0077] Patients can be identified as likely to experience toxicity, the type and grade of toxicity, and therefore monitoring, prevention, and treatment can be provided to the patient.

[0078] Currently, monitoring is required for all patients receiving CAR-T therapy at medical facilities, which results in significant costs. Using this technology, patients identified as not likely to experience toxicity can be monitored in an outpatient setting. Patients identified as likely to experience toxicity can be monitored as inpatients.

[0079] Preventive and / or therapeutic measures can also be taken for patients identified as likely to experience toxicity. Depending on the predicted toxicity, appropriate preventive / therapeutic measures can be taken. For example, for predicted CRS, tocilizumab 8 mg / kg can be administered intravenously over 1 hour (not to exceed 800 mg). Alternatively, dexamethasone 10 mg can be administered intravenously once daily. Methylprednisolone can also be used for more severe CRS.

[0080] For anticipated neurotoxicity, tocilizumab, dexamethasone, levetiracetam, corticosteroids, and / or methylprednisolone can be used. Alternative prophylactic / treatment options include anakinra, siltuximab, ruxolitinib, cyclophosphamide, IVIG (intravenous immunoglobulin), and ATG (antithymocyte globulin).

[0081] It is also known that severe CRS can be prevented by antihistamines or corticosteroids. Treatment for less severe CRS is symptomatic, addressing symptoms such as fever, muscle pain, or fatigue. Moderate CRS requires oxygen therapy and the administration of fluids and antihypertensive agents to increase blood pressure. For moderate to severe CRS, the use of immunosuppressants such as corticosteroids may be useful.

[0082] IL-6 inhibitors (e.g., anti-IL-6 antibodies such as tocilizumab) are known to be useful in preventing / treating CRS. GM-CSF inhibitors (e.g., anti-GM-CSF antibodies such as lenzilumab) may also be effective in preventing or managing cytokine release by reducing myeloid cell activation and decreasing the production of IL-1, IL-6, MCP-1, MIP-1, and IP-10.

[0083] Tocilizumab, dexamethasone, levetiracetam, lenzilumab, methylprednisolone, anakinra, siltuximab, ruxolitinib, cyclophosphamide, IVIG (intravenous immunoglobulin), and ATG (antithymocyte globulin).

[0084] Certain embodiments of the present disclosure relate to a method for identifying a patient as likely or unlikely to experience toxicity after cell therapy, the method comprising measuring a level of at least one of IL-15 (interleukin-15) and MCP-1 (monocyte chemoattractant protein-1) in a blood sample from the patient, and identifying the patient as likely to experience toxicity after cell therapy if the level of IL-15 or MCP-1 is higher than a corresponding reference level, or identifying the patient as not likely to experience toxicity after cell therapy if the level of IL-15 or MCP-1 is lower than the corresponding reference level. In certain such embodiments, the cell therapy comprises administration of immune cells.

[0085] Certain embodiments of the present disclosure relate to the above method, further comprising preventing or treating toxicity in the patient if the patient is identified as likely to experience toxicity.

[0086] Certain embodiments of the present disclosure relate to the above methods, wherein the treatment or prevention comprises administration of an agent selected from the group consisting of antihistamines, corticosteroids, antihypotensive agents, IL-6 inhibitors, GM-CSF inhibitors, and nonsteroidal anti-inflammatory drugs.

[0087] Certain embodiments of the present disclosure relate to the above methods, wherein the treatment or prevention comprises administration of an agent selected from the group consisting of tocilizumab, dexamethasone, levetiracetam, lenzilumab, methylprednisolone, anakinra, siltuximab, ruxolitinib, cyclophosphamide, IVIG (intravenous immunoglobulin), and ATG (antithymocyte globulin).

[0088] Certain embodiments of the present disclosure relate to the above method, wherein the immune cells comprise T cells engineered to express a chimeric antigen receptor (CAR).

[0089] Certain embodiments of the present disclosure relate to the above method, wherein the CAR has binding specificity for the CD19 (cluster of differentiation 19) protein.

[0090] Certain embodiments of the present disclosure relate to the above method, wherein the blood sample is a serum sample obtained from the patient prior to cell therapy.

[0091] Certain embodiments of the present disclosure relate to the above method, wherein the blood sample is obtained after the patient has undergone preconditioning treatment.

[0092] Certain embodiments of the present disclosure relate to the above method, wherein the preconditioning treatment reduces lymphocytes in the patient.

[0093] Certain embodiments of the present disclosure relate to the above method, wherein the toxicity is selected from the group consisting of cytokine release syndrome (CRS), neurological events (NE), and combinations thereof.

[0094] Certain embodiments of the present disclosure relate to the above method, wherein the toxicity is early-onset toxicity.

[0095] Certain embodiments of the present disclosure relate to the above method, wherein the early toxicity occurs within four days after cell therapy.

[0096] Certain embodiments of the present disclosure relate to the above methods, wherein the reference levels for IL-15 or MCP-1 are determined from patients who experience toxicity after cell therapy and patients who do not experience toxicity after cell therapy.

[0097] Certain embodiments of the present disclosure relate to the above methods, further comprising measuring the viability of cells used in the cell therapy, wherein if the IL-15 or MCP-1 levels are higher than the corresponding reference levels and the cell viability is higher than the reference cell viability, the patient is identified as likely to experience toxicity after the cell therapy, or if the IL-15 or MCP-1 levels are lower than the corresponding reference levels and the cell viability is lower than the reference cell viability, the patient is identified as not likely to experience toxicity after the cell therapy.

[0098] Certain embodiments of the present disclosure relate to the above method, further comprising obtaining one or more levels of baseline hemoglobin, baseline tumor burden, baseline LDH, baseline creatinine, and baseline calcium for the patient.

[0099] Certain embodiments of the present disclosure relate to a method for preventing or treating toxicity in a patient receiving cell therapy, comprising identifying a patient as likely or unlikely to experience toxicity following cell therapy by measuring the level of at least one of IL-15 (interleukin-15) and MCP-1 (monocyte chemoattractant protein-1) in a blood sample from the patient, and identifying the patient as likely to experience toxicity following cell therapy if the level of IL-15 or MCP-1 is higher than a corresponding reference level, or identifying the patient as not likely to experience toxicity following cell therapy if the level of IL-15 or MCP-1 is lower than the corresponding reference level. In such an embodiment, if the patient is identified as likely to experience toxicity following cell therapy, administering to the patient an agent that prevents or treats cytokine release syndrome (CRS) or a neurological event (NE).

[0100] Certain embodiments of the present disclosure relate to the above method, wherein the agent is selected from the group consisting of an antihistamine, a corticosteroid, an antihypotensive agent, an IL-6 inhibitor, a GM-CSF inhibitor, and a nonsteroidal anti-inflammatory drug.

[0101] Certain embodiments of the present disclosure relate to the above method, wherein the agent is selected from the group consisting of tocilizumab, dexamethasone, levetiracetam, lenzilumab, methylprednisolone, anakinra, siltuximab, ruxolitinib, cyclophosphamide, IVIG (intravenous immunoglobulin), and ATG (antithymocyte globulin).

[0102] Certain embodiments of the present disclosure relate to the above methods, further comprising measuring the viability of cells used in the cell therapy, wherein if the IL-15 or MCP-1 levels are higher than the corresponding reference levels and the cell viability is higher than the reference cell viability, the patient is identified as likely to experience toxicity after the cell therapy, or if the IL-15 or MCP-1 levels are lower than the corresponding reference levels and the cell viability is lower than the reference cell viability, the patient is identified as not likely to experience toxicity after the cell therapy.

[0103] Certain embodiments of the present disclosure relate to the above method, further comprising obtaining one or more levels of baseline hemoglobin, baseline tumor burden, baseline LDH, baseline creatinine, and baseline calcium for the patient. Kits and packages, software programs

[0104] The methods described herein can be carried out by utilizing pre-packaged diagnostic kits, such as those described below, that include at least one probe or primer nucleic acid described herein, which can be conveniently used, for example, to determine whether a subject has or is at risk of experiencing toxicity following cell therapy.

[0105] Accordingly, certain embodiments of the present disclosure relate to kits or packages useful for identifying patients likely to experience toxicity following cell therapy, the kits or packages comprising polynucleotide primers or probes or antibodies for measuring expression levels of IL-15 and MCP-1 in biological samples.

[0106] Diagnostic procedures can be performed in situ directly using mRNA isolated from cells or on tissue sections (fixed and / or frozen) of primary tissues, such as biopsies obtained from biopsies or resections, so that nucleic acid purification is not required. Nucleic acid reagents can be used as probes and / or primers for such in situ procedures.

[0107] In one embodiment, a kit or package useful for identifying patients who are or are not likely to experience toxicity following cell therapy is provided, the kit or package comprising polynucleotide primers or probes or antibodies for measuring expression levels of IL-15 and MCP-1 in a biological sample. In some embodiments, the kit or package further comprises an agent for measuring cell viability.

[0108] In one embodiment, the kit further comprises instructions for use. In one aspect, the kit comprises a manual comprising reference gene expression levels.

[0109] 8 is a block diagram illustrating a computer system 800 in which any embodiment of the present and related technology may be implemented. The computer system 800 includes a bus 802 or other communication mechanism for communicating information, and one or more hardware processors 804 coupled with the bus 802 for processing information. The hardware processors 804 may be, for example, one or more general-purpose microprocessors.

[0110] Computer system 800 also includes a main memory 806, such as a random access memory (RAM), cache, and / or other dynamic storage device, coupled to bus 802 for storing information and instructions executed by processor 804. Main memory 806 may also be used for storing temporary variables or other intermediate information during execution of instructions to be executed by processor 804. Such instructions, when stored on storage media accessible to processor 804, render computer system 800 a special-purpose machine that is customized to perform the operations specified in the instructions.

[0111] Computer system 800 further includes a read only memory (ROM) 808 or other static storage device coupled to bus 802 for storing static information and instructions for processor 804. A storage device 810, such as a magnetic disk, optical disk, or USB thumb drive (flash drive), is provided and coupled to bus 802 for storing information and instructions.

[0112] Computer system 800 may be coupled via bus 802 to a display 812, such as an LED or LCD display (or touch screen), for displaying information to a computer user. An input device 814, including alphanumeric and other keys, is coupled to bus 802 for communicating information and command selections to processor 804. Another type of user input device is a cursor control 816, such as a mouse, trackball, or cursor direction keys, for communicating directional information and command selections to processor 804 and for controlling cursor movement on display 812. In some embodiments, the same directional information and command selections as cursor control may be implemented via receiving touches on a touch screen without a cursor. Additional data may be retrieved from external data storage 818.

[0113] Computer system 800 may include a user interface module for implementing a GUI, which may be stored on a mass storage device as executable software code executed by a computing device. This and other modules may include, by way of example, components such as software components, object-oriented software components, class components, and task components, processes, functions, attributes, procedures, subroutines, segments of program code, drivers, firmware, microcode, circuits, data, databases, data structures, tables, arrays, and variables.

[0114] Generally, as used herein, the term "module" refers to logic embodied in hardware or firmware, or a collection of software instructions, possibly having entry and exit points, written in a programming language such as, for example, Java, C, or C++. Software modules may be compiled and linked into executable programs installed in dynamic link libraries, or may be written in an interpreted programming language such as, for example, BASIC, Perl, or Python. It will be understood that software modules may be callable from other modules or from themselves, and / or may be invoked in response to detected events or interrupts. Software modules configured to run on a computing device may be provided on a computer-readable medium such as a compact disc, digital video disc, flash drive, magnetic disk, or any other tangible medium, or as a digital download (which may originally be stored in a compressed or installable format that requires installation, decompression, or decryption before execution). Such software code may be partially or completely stored on the memory device of the running computing device for execution by the computing device. Software instructions may be embedded in firmware, such as an EPROM. It will further be understood that a hardware module may be composed of connected logic units such as gates and flip-flops, and / or may be composed of programmable units such as programmable gate arrays or processors. The modules or computing device functionality described herein are preferably implemented as software modules, but may also be represented in hardware or firmware. In general, modules described herein refer to logical modules that may be combined with other modules or divided into sub-modules, regardless of their physical organization or storage.In some embodiments, coding for the desired analysis is done in R Core Team (2019); language and environment for statistical computing (R Foundation for Statistical Computing, Vienna, Austria).

[0115] Computer system 800 may implement the techniques described herein using customized hardwired logic, one or more ASICs or FPGAs, firmware, and / or program logic that, in combination with the computer system, make computer system 800 a special-purpose machine or program. According to one embodiment, the techniques herein are performed by computer system 800 in response to processor 804 executing one or more sequences of one or more instructions contained in main memory 806. Such instructions may be read into main memory 806 from another storage medium, such as storage device 810. Execution of the sequences of instructions contained in main memory 806 causes processor 804 to perform the process steps described herein. In alternative embodiments, hardwired circuitry may be used in place of or in combination with software instructions.

[0116] As used herein, the term "non-transitory media" and similar terms refer to any medium that stores data and / or instructions that cause a machine to operate in a specific fashion. Such non-transitory media may include non-volatile media and / or volatile media. Non-volatile media include, for example, optical or magnetic disks, such as storage device 810. Volatile media includes dynamic memory, such as main memory 806. Common forms of non-transitory media include, for example, floppy disks, flexible disks, hard disks, solid-state drives, magnetic tape, or any other magnetic data storage medium, CD-ROMs, any other optical data storage medium, any physical medium with a pattern of holes, RAM, PROMs, and EPROMs, FLASH-EPROMs, NVRAMs, any other memory chips or cartridges, and network versions thereof.

[0117] Non-transitory media is distinct from but may be used in conjunction with transmission media. Transmission media involves transferring information between non-transitory media. For example, transmission media includes coaxial cables, copper wire and fiber optics, including the wires that comprise bus 802. Transmission media can also take the form of acoustic or light waves, such as those generated during radio wave and infrared data communications.

[0118] Various forms of media may be involved in carrying one or more sequences of one or more instructions to processor 804 for execution. For example, the instructions may initially be carried on a magnetic disk or solid state drive of a remote computer. The remote computer may load the instructions into its dynamic memory and use a component control to send the instructions over a telephone line. A component control local to computer system 800 may receive the data on the telephone line and use an infrared transmitter to convert the data to an infrared signal. An infrared detector can receive the data carried in the infrared signal and appropriate circuitry can place the data on bus 802. Bus 802 carries the data to main memory 806, from which processor 804 retrieves and executes the instructions. Instructions received by main memory 806 may be retrieved and executed. The instructions received by main memory 806 may optionally be stored on storage device 810 either before or after execution by processor 804.

[0119] Computer system 800 also includes a communication interface 818 coupled to bus 802. The communication interface 818 provides a two-way data communication coupling to one or more network links that are connected to one or more local networks. For example, the communication interface 818 may be an integrated services digital network (ISDN) card, a cable component control, a satellite component control, or a component control providing a data communication connection to a corresponding type of telephone line. As another example, the communication interface 818 may be a local area network (LAN) card that provides a data communication connection to a compatible LAN (or WAN component for communicating with a WAN). Wireless links may also be implemented. In any such implementation, the communication interface 818 sends and receives electrical, electromagnetic, or optical signals that carry digital data streams representing various types of information.

[0120] A network link typically provides data communication through one or more networks to other data devices. For example, a network link may provide a connection through a local network to a host computer or data equipment operated by an Internet Service Provider (ISP). The ISP then provides data communication services through the worldwide packet data communication network now commonly referred to as the "Internet." Both the local network and the Internet use electrical, electromagnetic or optical signals that carry digital data streams. The signals through the various networks and the signals on the network link and through communication interface 818, which carry the digital data to and from computer system 800, are exemplary forms of transmission media.

[0121] Computer system 800 can send messages and receive data, including program code, through the network(s), network link and communication interface 818. In the Internet example, a server might transmit a requested code for an application program through the Internet, an ISP, a local network and communication interface 818.

[0122] The received code may be executed by processor 804 as it is received and / or stored in storage device 810 or other non-volatile storage for later execution. Each of the processes, methods, and algorithms described in the previous sections may be embodied in, and fully or partially automated by, code modules executed by one or more computer systems or computer processors, including computer hardware. The processes and algorithms may be implemented partially or wholly in application-specific circuitry.

[0123] The various features and processes described above may be used independently of one another or may be combined in various ways. All possible combinations and subcombinations are intended to fall within the scope of the present disclosure. In addition, certain method or process blocks may be omitted in some implementations. The methods and processes described herein are also not limited to any particular order, and the associated blocks or states may be performed in other orders as appropriate. For example, the described blocks or states may be performed in an order other than the order specifically disclosed, or multiple blocks or states may be combined into a single block or state. Example blocks or states may be performed serially, in parallel, or in some other manner. Blocks or states may be added to or removed from the disclosed example embodiments. The example systems and components described herein may be configured differently from that described. For example, elements may be added, removed, or rearranged compared to the disclosed example embodiments.

[0124] Any process descriptions, elements, or blocks in the flow diagrams described herein and / or shown in the accompanying drawings should be understood as potentially representing modules, segments, or portions of code that comprise one or more executable instructions for implementing specific logical functions or steps in the process. As will be appreciated by those skilled in the art, alternative implementations are included within the scope of the embodiments described herein in which elements or functions are omitted and may be performed in a different order than that shown or discussed, including substantially concurrently or in reverse order, depending on the functionality involved.

[0125] It should be emphasized that many variations and modifications may be made to the above-described embodiments, and that the elements thereof should be understood as being among other acceptable examples. All such modifications and variations are intended to be included herein within the scope of the present disclosure. The foregoing description details certain specific embodiments of the present invention. However, no matter how detailed the above may be in the text, it will be understood that the present invention can be practiced in many ways. Also, as noted above, the use of a particular term when describing a particular feature or aspect of the present invention should not be construed as implying that the term has been redefined herein to be limited to including any specific characteristics of the feature or aspect of the invention to which the term relates. Therefore, the scope of the embodiments should be construed according to the appended claims and any equivalents thereof.

[0126] Various operations of the example methods described herein may be performed, at least in part, by one or more processors that are temporarily (e.g., by software) or permanently configured to perform the associated operations. Similarly, the methods described herein may be at least partially processor-implemented, with a particular processor or processors being an example of hardware. For example, at least some of the operations of the methods may be performed by one or more processors. Furthermore, one or more processors may also operate to support execution of the associated operations in a "cloud computing" environment or as "software as a service" (SaaS). For example, at least some of the operations may be performed by a group of computers (as examples of machines that include processors), and these operations are accessible via a network (e.g., the Internet) and one or more suitable interfaces (e.g., application program interfaces (APIs)). [Section 1] 1. A method for identifying a patient as likely or unlikely to experience toxicity following cell therapy, comprising: measuring the level of at least one of IL-15 (interleukin-15) and MCP-1 (monocyte chemotactic protein-1) in a blood sample from the patient; identifying the patient as likely to experience toxicity following the cell therapy if the level of IL-15 or MCP-1 is higher than a corresponding reference level, or identifying the patient as not likely to experience toxicity following the cell therapy if the level of IL-15 or MCP-1 is lower than a corresponding reference level; The method, wherein the cell therapy comprises administration of immune cells. [Section 2] 2. The method of claim 1, further comprising preventing or treating toxicity in said patient if said patient is identified as likely to experience said toxicity. [Section 3] Item 3. The method according to item 2, wherein the treatment or prevention comprises administering a drug selected from the group consisting of antihistamines, corticosteroids, antihypotensive agents, IL-6 inhibitors, GM-CSF inhibitors, and nonsteroidal anti-inflammatory drugs. [Section 4] Item 4. The method according to Item 3, wherein the treatment or prevention comprises administration of a drug selected from the group consisting of tocilizumab, dexamethasone, levetiracetam, lenzilumab, methylprednisolone, anakinra, siltuximab, ruxolitinib, cyclophosphamide, IVIG (intravenous immunoglobulin), and ATG (antithymocyte globulin). [Section 5] Item 5. The method according to any one of Items 1 to 4, wherein the immune cells comprise T cells engineered to express a chimeric antigen receptor (CAR). [Section 6] The method of paragraph 5, wherein the CAR has binding specificity for CD19 (cluster of differentiation 19) protein. [Section 7] Item 7. The method according to any one of Items 1 to 6, wherein the blood sample is a serum sample obtained from the patient before the cell therapy. [Section 8] Item 8. The method of item 7, wherein the blood sample is obtained after the patient has undergone preconditioning treatment. [Section 9] The method of paragraph 8, wherein the preconditioning treatment reduces lymphocytes in the patient. [Section 10] Item 10. The method according to any one of items 1 to 9, wherein the toxicity is selected from the group consisting of cytokine release syndrome (CRS), neurological events (NE), and combinations thereof. [Section 11] Item 11. The method of item 10, wherein the toxicity is early-onset toxicity. [Section 12] Item 12. The method of paragraph 11, wherein the early toxicity occurs within 4 days after the cell therapy. [Section 13] Item 13. The method according to any one of Items 1 to 12, wherein the reference levels for IL-15 or MCP-1 are determined from patients who experience the toxicity after the cell therapy and patients who do not experience the toxicity after the cell therapy. [Section 14] Item 14. The method according to any one of Items 1 to 13, further comprising measuring the viability of cells used in the cell therapy, wherein if the IL-15 or MCP-1 level is higher than the corresponding reference level and the cell viability is higher than the reference cell viability, the patient is identified as having a high likelihood of experiencing toxicity after the cell therapy, or if the IL-15 or MCP-1 level is lower than the corresponding reference level and the cell viability is lower than the reference cell viability, the patient is identified as not having a high likelihood of experiencing toxicity after the cell therapy. [Section 15] 15. The method of any one of paragraphs 1 to 14, further comprising obtaining one or more levels of baseline hemoglobin, baseline tumor burden, baseline LDH, baseline creatinine, and baseline calcium for the patient. [Section 16] 1. A method for preventing or treating toxicity in a patient receiving cell therapy, comprising: identifying the patient as likely or unlikely to experience toxicity following cell therapy; measuring the level of at least one of IL-15 (interleukin-15) and MCP-1 (monocyte chemotactic protein-1) in a blood sample from the patient; identifying the patient as likely to experience toxicity following the cell therapy if the level of IL-15 or MCP-1 is higher than a corresponding reference level, or identifying the patient as not likely to experience toxicity following the cell therapy if the level of IL-15 or MCP-1 is lower than a corresponding reference level; and if the patient is identified as likely to experience toxicity following the cell therapy, administering to the patient an agent that prevents or treats cytokine release syndrome (CRS) or a neurological event (NE). [Section 17] Item 17. The method according to Item 16, wherein the drug is selected from the group consisting of antihistamines, corticosteroids, antihypotensive agents, IL-6 inhibitors, GM-CSF inhibitors, and nonsteroidal anti-inflammatory drugs. [Section 18] Item 17. The method of item 16, wherein the drug is selected from the group consisting of tocilizumab, dexamethasone, levetiracetam, lenzilumab, methylprednisolone, anakinra, siltuximab, ruxolitinib, cyclophosphamide, IVIG (intravenous immunoglobulin), and ATG (antithymocyte globulin). [Section 19] 17. The method of claim 16, further comprising measuring the viability of cells used in the cell therapy, wherein if the IL-15 or MCP-1 level is higher than the corresponding reference level and the cell viability is higher than the reference cell viability, the patient is identified as having a high likelihood of experiencing toxicity after the cell therapy, or if the IL-15 or MCP-1 level is lower than the corresponding reference level and the cell viability is lower than the reference cell viability, the patient is identified as not having a high likelihood of experiencing toxicity after the cell therapy. [Section 20] 20. The method of any one of paragraphs 16 to 19, further comprising obtaining one or more levels of baseline hemoglobin, baseline tumor burden, baseline LDH, baseline creatinine, and baseline calcium for the patient. [Section 21] A kit or package useful for identifying patients who are likely to experience toxicity after cell therapy, the kit or package comprising polynucleotide primers or probes or antibodies for measuring the expression levels of IL-15 and MCP-1 in a biological sample. [Example]

[0127] The following examples are included to demonstrate specific embodiments of the present disclosure. It should be understood by those skilled in the art that the techniques disclosed in the following examples represent well-functioning techniques in the practice of the present disclosure and can therefore be considered to constitute specific modes for its practice. However, those skilled in the art should, in light of the present disclosure, understand that many changes can be made in the specific embodiments disclosed that will still achieve similar or similar results without departing from the spirit and scope of the present disclosure. Example 1: Prediction of premature cytokine release syndrome and neurological events after axicabtagene ciloreucel in large B-cell lymphoma based on machine learning algorithms

[0128] In the clinical trial ZUMA-1, a pivotal study of axi-cel in patients with refractory large B-cell lymphoma (LBCL), grade 3 or higher cytokine release syndrome (CRS) and neurologic events (NE) occurred in 13% and 28% of patients, respectively, requiring intensive inpatient management. With increasing safety experience, management of CRS and NE has been evaluated in several exploratory safety management cohorts in ZUMA-1. Cohort 4 evaluated the use of levetiracetam prophylaxis and early corticosteroids and / or tocilizumab on the incidence and severity of CRS and NE. The impact of adding prophylactic corticosteroids to the toxicity management regimen in Cohort 4 was evaluated in Cohort 6. Of note, some treated patients had early-onset versus late-onset CRS or NE, warranting separate management. To facilitate toxicity management, this example developed a predictive algorithm for early-onset acute toxicity (within 3–4 days after axi-cel) based on machine learning from ZUMA-1 data.

[0129] Methods: This post-hoc analysis included patients from cohorts 1, 2, 4, and 6 of ZUMA-1's phase 1 and phase 2 trials. Covariates (>1500; 227 measured before axi-cel infusion) included baseline product, patient, and tumor characteristics, and inflammatory soluble blood biomarker levels. Data from patients in cohorts 1, 2, and 4 were randomly divided into a training set (70%) and a test set (30%). Univariate and multivariate analyses and clinical feasibility considerations were applied to select a subset of covariates for further analysis. Machine learning (e.g., logistic regression, random forest, XGBoost, and AdaBoost classifiers) was applied to three categories of covariates (1, clinical; 2, mechanistic [e.g., product attributes, inflammatory blood biomarkers]; 3, hybrid of 1 and 2) to construct the best-performing model (predictive performance assessed by the area under the curve [AUC] for the test data). The optimal cutoff for the prediction score was selected by receiver operating characteristic (ROC) or classification tree analysis. Data from patients in Cohort 6 were included to validate the best-performing model generated using the training data.

[0130] Results: Multivariate analysis and machine learning from data obtained from 149 evaluable patients in cohorts 1, 2, and 4 of ZUMA-1 yielded several comparable predictive models for early-onset CRS or NE (best-performing models with ROC AUCs of >0.8 in training and >0.7 in testing). Covariates in the best-performing models included product cell viability, centrally measured IL-15 and CCL2 (MCP-1) serum levels on day 0 (before axi-cel treatment) and locally measured blood counts, blood chemistry analytes, tumor burden, and serum lactate dehydrogenase levels. The best-performing models with fewer than five covariates contained only mechanistic covariates or hybrid mixes of covariates. A three-covariate mechanistic model (product cell viability and day 0 IL-15 and CCL2 (MCP-1) serum levels, all positively associated with early toxicity) performed comparably to the larger best-performing model (ROC AUC >0.7 in the study). Classification trees partitioned based on day 0 IL-15 and product cell viability showed potential for stratifying patients by early versus late onset toxicity (specificity >0.85).

[0131] Machine learning applied to covariates measured before axi-cel infusion yielded predictive models of early-onset CRS or NE that could be used for toxicity prediction, monitoring, and management. High-performance hybrid or mechanistic models confirmed the importance of conditioning-related increases in T cell viability (product cytocompatibility) and factors (IL-15 and CCL2) that influence toxicity. Example 2: Premature Cytokine Release Syndrome and Prediction of Neurological Events

[0132] This example describes the data used to build the algorithm in Example 1 and the procedures for developing the predictive algorithm, including feature screening and selection, multivariate modeling, model evaluation, and classification of a test population by the predictive algorithm. data

[0133] All analyses were performed on the safety analysis set of ZUMA1 patients (i.e., received any dose of axicabtageneciloleucel) with a cutoff date of November 6, 2019.

[0134] Populations included: (a) Phase 1 at the 36-month cutoff and Cohort 1 and Cohort 2 in Phase 2 (Phase 1 had 7 subjects with DLBCL, PMBCL, or TFL; Phase 2 Cohort 1 had 77 subjects with refractory DLBCL; Phase 2 Cohort 2 had 24 subjects with refractory PMBCL and TFL); (b) Phase 2 Cohort 3 (38 subjects with relapsed or refractory transplant-ineligible DLBCL, PMBCL, or TFL); and (c) Phase 2 Cohort 4 (41 subjects with relapsed or refractory DLBCL, PMBCL, TFL, or HGBCL after two or more lines of systemic therapy).

[0135] The following time frames were considered: 1, day 0, day 1, day 2; 2, day 0, day 1, day 2, day 3; and day 0, day 1, day 2, day 3, day 4. For each of the above time frames, the following three outpatient definitions were defined (see Figure 1 and Table 1): Definition A: Patients who meet both (a) worst grade 1 or no CRS (i.e., worst CRS grade 1 or less) and (b) no neurological events (NE) during a given time frame; Definition B: Patients without any episodes of CRS or NE during a given time frame; Definition C (proposed by Medical Affairs and Clinical Research).

[0136] Patients who did not meet the above "outpatient" criteria were assigned as "inpatients" for each definition. [Table 1] Note: In definition C, the time frame is a condition of the "outpatient" or "inpatient" definition. For example, if days 0-2 are given, all criteria are confirmed within days 0, 1, and 2 after infusion. Covariate and feature selection

[0137] Covariates (or >1500 measured before axi-cel infusion 227) included baseline product, patient and tumor characteristics, and inflammatory soluble blood biomarker levels. Major categories of covariates or analytes included: Baseline characteristics, such as ECOG performance, disease type, disease stage, International prognostic index (IPI) category, tumor burden, etc.; laboratory analytes in both chemistry and hematology; serum cytokines and inflammatory markers; Product characteristics, including product cell viability, CD4 and CD8 counts and percentages, as well as CD4 / CD8 ratios, phenotypes / regated phenotypes for CD4 and CD8, IFN-gamma in co-culture, etc.; and Cell proliferation information, including cell doubling time (in days) and proliferation rate.

[0138] The data were randomly split into a training set (e.g., 70% of the samples) to fit the model, and a test set (e.g., the remaining 30% of the samples) was used to provide an unbiased assessment of model performance. Univariate Screening

[0139] Univariate analyses of each covariate are performed one at a time, where the association of the covariate with outpatient / inpatient status is assessed, and those variables that pass screening criteria are selected for use in multivariate modeling. Analytical approach to feature selection

[0140] After performing K-Nearest Neighbor (KNN) imputation for missing data, the following statistical and model-based approaches were applied to features that passed univariate screening. Features were ranked and the top-ranked features were selected by each of these approaches. Features selected by three, four, or all five of the methods described below can be considered "analytically significant" features.

[0141] Weight of evidence and information value: Weight of evidence (WOE) + information value (IV) is a simple method used to estimate the predictive power of a feature for an outcome of interest. WOE divides the data for each feature into a number of bins (e.g., j = 10 bins) and calculates the predictive power (i.e., "evidence") of the feature for the outcome within each bin. Then, for each feature, IV combines the WOEs of all bins into a single score, which is IV = Σ j (Proportion of non-events j -Percentage of events j ) * WOE j Features with higher IV values ​​are selected as candidates for the machine learning model (e.g., an IV value of 0.3 or greater or 0.5 or greater is considered "moderately good" or "good," respectively).

[0142] SelectkBest by analysis of variance: SelectkBest is a univariate feature selection method used to identify features that best explain outcome. Specifically, for each feature, an analysis of variance (ANOVA) was performed and the corresponding F-statistic, which represents the ratio of explained to unexplained variation between the feature and outcome, was calculated. The SelectKBest function then selected the feature with the k highest scores, e.g., lowest p-value, as the "best" feature.

[0143] Extra Trees Classifier: Extra Trees Classifier (also known as Extremely Randomized Trees) is a type of ensemble learning technique that aggregates the results of many uncorrelated decision trees into a "forest" to output a classification result. Gini importance can be used to select the features (e.g., 30 features) that have the highest importance in predicting outcome.

[0144] Recursive Feature Elimination (RFE): Recursive feature elimination (RFE) is applied to the fitted model with importance weights assigned to the features (e.g., model coefficients, importance attributes) to eliminate the worst performing features for the model until the desired number of features is achieved. The top ranked features, e.g., 30 features, may be selected for model building.

[0145] RFE-based logistic regression: RFE was applied to a logistic regression model with variable importance defined by the model coefficients.

[0146] RFE-based random forest: RFE was applied to models estimated using random forest, where splits were determined using a specific criterion (e.g., the Gini index was used as the default) and variable importance was assessed using feature importance scores. Feature selection by subject matter experts (SMEs)

[0147] Subject matter experts (SMEs) will review the list of analytically significant features from the univariate and multivariate approaches, consider clinical feasibility, and provide the following three categories of covariates for further analysis: clinical covariates, e.g., tumor-related (LDH, volume), disease stage, blood counts (WBC, RBC), cell-related analytes (Hgb), analytes related to metabolic status; mechanistic covariates, such as product cell viability, IL-15 on day 0, MCP-1 on day 0, cytokines, chemokines, and other product attributes; and Hybrid (clinical + mechanical) covariates.

[0148] A list of covariates was generated as imported candidates for classification model building. Multivariate modeling with machine learning algorithms

[0149] Five machine learning algorithms were applied to the covariates in each of these lists (clinical covariates, mechanical covariates, and hybrid). All classification algorithms rely on a set of hyperparameters that are "tuned" to find the combination that results in optimal performance. The model with the best predictive performance among the five machine learning algorithms was considered the best performing model (BPM). A brief description of these machine learning algorithms follows:

[0150] Logistic Regression: Logistic regression is a parametric method that models the log-odds of the probability of a binary event occurring as a linear combination of features. Our approach uses a random undersampled dataset that is fed into a logistic regression algorithm, which we call LOGREGRUS (Logistic Regression with Random Under Sampling).

[0151] Random Forest: Random forest is an ensemble learning method designed to reduce the variance that can result from a single model (i.e., a decision tree). Random forest classification utilizes bootstrap aggregation (bagging), a technique that first bootstraps training data, makes predictions, and then aggregates the results from individual models to make overall more accurate predictions. This example used a randomly undersampled dataset fed into the random forest algorithm, called RFCRUS (Random Forest Classifier with Random Under Sampling).

[0152] Extreme Gradient Boosting (XGBoost): Boosting is an ensemble machine learning technique in which many weak learners (e.g., decision trees) are iteratively combined to form a final strong learner. Models are added sequentially until no further improvement can be made. Gradient boosting refers to an implementation of boosting that uses any differentiable loss function and a gradient descent optimization algorithm. Extreme Gradient Boosting refers to a fast and efficient implementation of the gradient boosting algorithm. This example used a randomly undersampled dataset fed into XGBoost, called XGBCRUS (XGBoost Classifier with Random Under Sampling).

[0153] Balanced Random Forest Classifier (BRFC): A Balanced Random Forest Classifier (BRFC) differs from a Random Forest classifier in that it uses a balanced bootstrap sample of the training data, which differs from a random under-sampled dataset fed to a Random Forest algorithm because it does not pre-process the training data before learning the Random Forest classifier.

[0154] Random Under-Sampling Boosting Classifier (RUSBoost): Adaptive boosting (AdaBoost) is an ensemble boosting machine learning method that attempts to combine multiple weak classifiers (i.e., decision strains) into a single strong classifier. It adaptively reweights training samples based on classifications from previous learners, with more weight given to misclassified samples. The final prediction is a weighted average of all weak learners, with more weight given to strong learners. Random Under-Sampling Boost (RUSBoost) adapts AdaBoost to cases with imbalanced data by randomly undersampling at each iteration of the boosting algorithm. Model evaluation

[0155] Receiver Operating Characteristic (ROC) and AUC: Receiver operating characteristic (ROC) curves are a method for evaluating and comparing the performance of classification models. The false positive and true positive rates for a classifier are evaluated over a grid of possible (predicted probability) cutpoints that define whether an observation is classified as an event or non-event, and these values ​​are plotted. The area under the ROC curve (AUC) can also be calculated.

[0156] Tables 2-6 show selected covariates and AUC from BPM, where BPM is selected as having the highest AUC from the test data among the five machine learning algorithms. [Table 2] Covariates that were positively and negatively associated with all nine outpatient definitions are indicated by ↑ and ↓, respectively. Covariates that had different directions of association across the nine outpatient definitions were

number

[0157] Once the best covariates were identified, the present example applied two approaches to classify the test population: The performance of the classification on the test population was measured by a confusion matrix.

[0158] Confusion Matrix: A confusion matrix for a classifier summarizes the number of correct and incorrect predictions per class in the form of a contingency table. A confusion matrix is ​​useful for understanding the predictive accuracy of a classifier and the types of errors it is likely to make. Accuracy (accuracy represents the proportion of observations that are correctly classified into the true class, either positive or negative), sensitivity (true positive rate), and specificity (true negative rate) are calculated from the numbers in the confusion matrix. Model-based approach

[0159] In this example, BPM was applied to the training data to obtain predicted probabilities, and then an ROC curve was created based on the predicted probabilities of subjects from the training data, and the optimal cut-off point was selected as the cut-off value at which the Youden index was maximized (Youden index = sensitivity + specificity - 1). Subjects with predicted probabilities above this cut-off value were classified as "outpatients". Other patients were classified as "inpatients".

[0160] BPM for A3: For the minimal mechanistic model for outpatient-defined A3 (with covariates of cell viability + IL-15 on day 0 + MCP-1 on day 0), this example selected Random Forest (RF) as the best-performing algorithm. The ROC and boxplots (RFCRUS, optimal cutoff: 0.538) of BPM are shown in Figures 2 and 3 along with cell viability + IL-15 + MCP-1 for outpatient A3. The confusion matrix is ​​shown in Table 7. [Table 7] Sensitivity: 0.7115, specificity: 0.7500, accuracy: 0.7308 Subjects with a predicted probability greater than 0.538 are classified as "outpatients"

[0161] Test data with cell viability + IL-15 + MCP-1 for outpatient A3, boxplot of predictions for BPM is shown in Figure 4. The confusion matrix is ​​shown in Table 7. [Table 8] Sensitivity: 0.7000, specificity: 0.7143, accuracy: 0.7073 Subjects with a predicted probability greater than 0.538 are classified as "outpatients" Tree-based approach

[0162] This example then constructed a decision tree by splitting the best selected covariates in the training data, which constituted the root node of the tree, into subsets that constituted successors. The splitting was based on a set of splitting rules based on classification features. A decision tree can be described as a combination of splits on the best selected covariates to classify subjects to achieve high accuracy. The resulting decision tree is illustrated in Figure 5 (training data) and Figure 6 (test data). The corresponding confusion matrices are shown in Tables 9 and 10. [Table 9] Sensitivity: 0.6275, specificity: 0.7500, accuracy: 0.6916 [Table 10] Sensitivity: 0.6000, specificity: 0.9048, accuracy: 0.7561 Direction

[0163] This example then used partial dependence plots to show the relationship between oncotoxicity and covariates by leveraging the effects of other covariates in the machine learning model. The plots are presented in Figure 7. The plots suggest that the cutoff values ​​for cell viability are approximately 95%, for IL-15 are approximately 28 pg / mL, and for CCL2 are approximately 1300 pg / mL.

[0164] The direction of the covariates associated with the onset of toxicity can also be indicated by the estimated coefficients in the logistic regression of outpatient (yes / no) ~ cell viability + IL-15 + MCP-1. Negative coefficients indicate that all three covariates were positively associated with early-onset toxicity (Table 11). [Table 11] * * *

[0165] Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs.

[0166] The invention illustratively described herein may suitably be practiced in the absence of any element or elements, limitation or limitations not specifically disclosed herein. Thus, for example, terms such as "comprising," "including," and "containing" are to be read expansively and not limiting. Furthermore, the terms and phrases used herein are used as terms of description and not of limitation, and there is no intention to use such terms and phrases to exclude any equivalents of the features shown and described, or portions thereof, although it is recognized that various modifications are possible within the scope of the claimed invention.

[0167] Thus, while the present invention has been specifically disclosed in terms of preferred embodiments, it is to be understood that optional features, modifications, improvements, and variations of the invention embodied herein as disclosed herein may be employed by those skilled in the art, and that such modifications, improvements, and variations are deemed to be within the scope of the present invention. The materials, methods, and examples provided herein are representative of preferred embodiments and are illustrative and not intended as limitations on the scope of the invention.

[0168] The invention has been described broadly and generically herein. Each of the narrower species and subgeneric groupings falling within the generic disclosure also form part of the invention. This includes the generic description of the invention with any condition or negative limitation removing any subject matter from the genus, regardless of whether the omitted material is specifically set forth herein.

[0169] Additionally, when features or aspects of the invention are described in terms of a Markush group, those skilled in the art will recognize that the invention is also described in terms of any individual member or subgroup of members of the Markush group.

[0170] All publications, patent applications, patents, and other references mentioned herein are expressly incorporated by reference in their entirety to the same extent as if each were individually incorporated by reference. In case of conflict, the present specification, including definitions, will control.

[0171] While the present disclosure has been described in conjunction with the above embodiments, it should be understood that the foregoing description and examples are intended to be illustrative and not limiting of the scope of the present disclosure. Other aspects, advantages, and modifications within the scope of the present disclosure will be apparent to those skilled in the art to which this disclosure pertains.

Claims

1. 1. A method for identifying a patient as likely or unlikely to experience toxicity following cell therapy, comprising: measuring the level of at least one of IL-15 (interleukin-15) and MCP-1 (monocyte chemotactic protein-1) in a blood sample obtained from the patient prior to the cell therapy; a level of IL-15 or MCP-1 higher than the corresponding reference level indicates that the patient is likely to experience toxicity following the cell therapy; a level of IL-15 or MCP-1 lower than the corresponding reference level indicates that the patient is not likely to experience toxicity following the cell therapy; The method, wherein the cell therapy comprises administration of immune cells.

2. 10. The method of claim 1 for providing prevention or treatment of toxicity to a patient identified as likely to experience said toxicity.

3. 3. The method of claim 2, wherein the prevention or treatment comprises administration of a drug selected from the group consisting of antihistamines, corticosteroids, antihypotensive agents, IL-6 inhibitors, GM-CSF inhibitors, and nonsteroidal anti-inflammatory drugs.

4. 4. The method of claim 3, wherein the prevention or treatment comprises administration of a drug selected from the group consisting of tocilizumab, dexamethasone, levetiracetam, lenzilumab, methylprednisolone, anakinra, siltuximab, ruxolitinib, cyclophosphamide, IVIG (intravenous immunoglobulin), and ATG (antithymocyte globulin).

5. 5. The method of any one of claims 1 to 4, wherein the immune cells comprise T cells engineered to express a chimeric antigen receptor (CAR).

6. 6. The method of claim 5, wherein the CAR has binding specificity for CD19 (cluster of differentiation 19) protein.

7. The method of any one of claims 1 to 4, wherein the blood sample is obtained after a preconditioning treatment of the patient.

8. 8. The method of claim 7, wherein the preconditioning therapy reduces lymphocytes in the patient.

9. 5. The method of any one of claims 1 to 4, wherein the toxicity is selected from the group consisting of cytokine release syndrome (CRS), neurological events (NE), and combinations thereof.

10. 10. The method of claim 9, wherein the toxicity is early-onset toxicity.

11. 11. The method of claim 10, wherein the early toxicity occurs within four days after the cell therapy.

12. 5. The method of any one of claims 1 to 4, wherein the reference levels for IL-15 or MCP-1 are determined from patients who experience said toxicity after said cell therapy and patients who do not experience said toxicity after said cell therapy.

13. measuring the viability of cells used in the cell therapy, where a level of IL-15 or MCP-1 higher than the corresponding reference level and a cell viability higher than the reference cell viability indicate that the patient is likely to experience toxicity following the cell therapy; 5. The method of any one of claims 1 to 4, wherein when the level of IL-15 or MCP-1 is lower than the corresponding reference level and the cell viability is lower than the reference cell viability, it indicates that the patient is not likely to experience toxicity following the cell therapy.

14. 5. The method of any one of claims 1-4, further comprising obtaining one or more levels of baseline hemoglobin, baseline tumor burden, baseline LDH, baseline creatinine, and baseline calcium for the patient.

15. 1. A composition for the prevention or treatment of cytokine release syndrome (CRS) or neurological events (NE) in patients identified as likely to experience toxicity following cell therapy, comprising: comprising a drug selected from the group consisting of antihistamines, corticosteroids, antihypotensives, IL-6 inhibitors, GM-CSF inhibitors, and nonsteroidal anti-inflammatory drugs; wherein the patient is identified as likely to experience toxicity after the cell therapy if the level of IL-15 (interleukin-15) or MCP-1 (monocyte chemotactic protein-1) in a blood sample obtained from the patient before the cell therapy is higher than the corresponding reference level, or the patient is identified as not likely to experience toxicity after the cell therapy if the level of IL-15 or MCP-1 in a blood sample obtained from the patient before the cell therapy is lower than the corresponding reference level. The composition.

16. 16. The composition of claim 15, comprising an agent selected from the group consisting of tocilizumab, dexamethasone, levetiracetam, lenzilumab, methylprednisolone, anakinra, siltuximab, ruxolitinib, cyclophosphamide, IVIG (intravenous immunoglobulin), and ATG (antithymocyte globulin).

17. The composition of claim 15, wherein the patient is identified as having a high likelihood of experiencing toxicity after the cell therapy when the IL-15 or MCP-1 level is higher than the corresponding reference level and the viability of cells used in the cell therapy is higher than the reference cell viability, or the patient is identified as not having a high likelihood of experiencing toxicity after the cell therapy when the IL-15 or MCP-1 level is lower than the corresponding reference level and the viability of cells used in the cell therapy is lower than the reference cell viability.

18. 18. The composition of any one of claims 15-17, further comprising obtaining one or more levels of baseline hemoglobin, baseline tumor burden, baseline LDH, baseline creatinine, and baseline calcium for the patient.

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