167 results about "Hematological Tumor" patented technology

The invention discloses a blood tumor patient clinical data analysis method and system based on a knowledge graph, and relates to the technical field of medical information processing. The method comprises the following steps: analyzing an unstructured text by utilizing a natural language processing model, and constructing a standardized entity set; aggregating laboratory indexes through a dynamic window, and constructing a time axis data set for marking a treatment stage; a standardized entity is integrated based on a blood tumor ontology model, a dynamic global knowledge graph is constructed in combination with a clinical causal relationship and a time sequence path, and chain reaction early warning is realized; based on the real-time patient sub-atlas, successful cases with the same molecular features are retrieved in the knowledge atlas to generate a candidate treatment scheme set, a graph neural network trained through an optimization algorithm is utilized to predict the complication risk of each scheme, and finally the optimal treatment scheme is evaluated and selected; according to the method, a clinical data barrier is broken through, dynamic reasoning, advanced risk early warning and personalized scheme optimization of the whole treatment cycle are realized, and the diagnosis and treatment accuracy, safety and medical resource utilization efficiency are remarkably improved.

The invention belongs to the technical field of data analysis, and discloses a clinical data analysis method and system for a hematologic tumor patient. The method comprises the following steps: creating an OPC UA information instance of a clinical data acquisition device, and constructing a blood tumor knowledge graph, a clinical data analysis model and a data acquisition optimization model; collecting real-time clinical data of a hematologic tumor patient, encrypting and uploading the real-time clinical data to the cloud data center; writing the real-time clinical data into the corresponding OPC UA information instance, and extracting real-time OPC UA information data; according to the real-time OPC UA information data and the blood tumor knowledge map, using a clinical data analysis model to perform clinical data analysis; and performing data acquisition optimization by using the data acquisition optimization model according to a real-time clinical data analysis result. According to the invention, the problems of insufficient accuracy, low data processing efficiency and low intelligent degree in the prior art are solved.

The invention provides a hematologic tumor cord blood transplantation treatment prognosis risk assessment method and system based on multi-modal data fusion, a medium and electronic equipment, and relates to the technical field of medical artificial intelligence and clinical decision support systems. The method comprises the following steps: acquiring multi-modal data including unit characteristic data of cord blood of a patient, biomarker data and the like; screening out a simplified feature set from the preprocessed multi-modal data; fusing the simplified features based on three complementary strategies of feature level direct cascade, knowledge graph semantic association and multi-model decision integration; and a prediction model is constructed, and a standardized risk assessment report is generated based on the optimized hierarchical risk levels and is used for assisting clinical decision support. According to the method, accurate layering of the prognosis risk of the hematologic tumor umbilical cord blood transplantation patient is achieved, high-accuracy risk prediction is provided, good interpretability and personalized decision support capacity are achieved, and a scientific basis is provided for clinical practice.

The invention relates to the technical field of disease curative effect evaluation, and discloses a method for evaluating the curative effect of granulocyte deficiency accompanying fever after hematologic tumor chemotherapy based on machine learning, and the method comprises the steps: S1, collecting and preprocessing multi-center medical data, the data comprising structured clinical data and multi-modal unstructured data; s2, a curative effect prediction model is constructed based on a graph neural network, and a central moment constraint-based graph federal learning training model is adopted, wherein a patient graph is constructed as an original graph and an enhanced graph is generated; respectively processing the original image and the enhanced image through a two-channel image convolutional neural network, and extracting a high-order representation vector; constructing an enhanced perception loss function based on the high-order representation vectors of the original image and the enhanced image; combining a federated learning framework with multi-center data to train a model; and S3, predicting a curative effect evaluation result through the trained curative effect prediction model. The accuracy, the stability and the clinical interpretability of curative effect evaluation are improved.

Systems and methods for determining a blood tumor mutational burden (bTMB) for a test subject are provided in which there is obtained, from a panel-enriched sequencing reaction, a plurality of nucleic acid sequences. The plurality of nucleic acid sequences comprises a corresponding sequence for each cell-free DNA fragment in a plurality of cell-free DNA fragments obtained from a liquid biopsy sample from the test subject. Each respective cell-free DNA fragment in the plurality of cell-free DNA fragments corresponds to a respective probe sequence in a plurality of probe sequences used to enrich cell-free DNA fragments in the liquid biopsy sample in the panel-enriched sequencing reaction. There is determined, using the panel-enriched sequencing reaction, that a circulating tumor fraction (ctFE) is above a threshold ctFE value. Responsive to this determination, the bTMB is calculated for the test subject from the panel-enriched sequencing reaction and reported.

The invention relates to a DNMT1-HDAC double-target inhibitor as shown in a formula (I) as well as a preparation method and application thereof, and the DNMT1-HDAC double-target inhibitor not only shows good DNMT1 and HDAC enzyme inhibition activity, but also has remarkable anti-tumor activity on solid tumors and hematoma. As a double-target inhibitor based on DNMT1 and HDACs reported for the first time, the compound has a great prospect in the aspect of cancer treatment; # imgabs0 #

The invention discloses a blood tumor fusion gene minimal residual focus monitoring method, system and equipment, and the key points of the technical scheme are as follows: obtaining fusion gene information and high-throughput sequencing data of all genetic information; under the condition that the high-throughput sequencing data is subjected to PCR without duplicate removal, comparing the high-throughput sequencing data to a reference genome to obtain a first comparison result, screening out a real fusion gene sequence from the first comparison result, and calculating to obtain a first copy number of a fusion gene according to the real fusion gene sequence; a real housekeeping gene sequence is screened out from the first comparison result, and a second copy number of housekeeping genes is calculated according to the real housekeeping gene sequence; dividing the first copy number by the second copy number to obtain the minimal residual focus ratio of the fusion gene. According to the invention, high-sensitivity and high-specificity monitoring of MRD can be realized.

The invention belongs to the technical field of biomedical detection, and discloses a Raman spectrum analysis device for quantitative detection of hematologic tumor markers, which comprises a blood collection centrifugal unit with a self-adaptive load regulation mechanism for monitoring blood density and components in real time, centrifugal force and time parameters are automatically adjusted according to the blood density and components; the optical fiber Raman spectrometer is provided with an automatic wavelength calibration system, and an ultrafast laser pulse transmitter and a high-sensitivity photon counting detector are integrated on the optical fiber Raman spectrometer. Raman scattering signals are enhanced by adopting a quantum entanglement light source and a nonlinear optical crystal; according to the invention, the detection capability on low-concentration tumor markers can be obviously improved. Due to the improvement, the device can accurately detect the existence of the tumor marker at the early stage of cancer, and powerful support is provided for early treatment of a patient.

The invention discloses a hematologic tumor calming treatment and protection intervention method based on potential profile analysis, and relates to the technical field of medical treatment and health information analysis, and the method comprises the following steps: S1, constructing a multi-dimensional intervention feature data set; s2, constructing a profile analysis model according to the feature data set; s3, performing category stability verification according to a section analysis result; s4, screening an intervention reference template according to a stability verification result; s5, matching individual features according to the intervention reference template to form a preset intervention path; s6, constructing a profile-driven path execution and feedback control system by using an intervention preset path; by setting a profile response function modeling model and combining a multi-intervention feature matrix to construct a high-resolution profile function, the problem that an existing profile division model is insufficient in continuous variable processing capacity is effectively solved, the profile structure expression capacity and individual heterogeneity description precision are improved, and the profile division efficiency is improved. The method is suitable for the fine layered modeling requirement under the driving of multi-dimensional intervention features.

The invention relates to a tumor curative effect evaluation method and system based on a medical image, and the method comprises the steps: obtaining a first PET-CT image and a second PET-CT image of a blood system tumor patient before and after the treatment process, and determining the focus change information of a focus region based on the first PET-CT image and the second PET-CT image; performing maximum density projection on the first PET-CT image and / or the second PET-CT image along different directions to generate maximum density projection images of a plurality of visual angles; determining global image information of a focus area based on the maximum density projection images of the multiple visual angles; determining a multi-dimensional score corresponding to the curative effect of the tumor patient based on the global image information; and fusing the focus change information and the multi-dimensional score to generate tumor curative effect evaluation information.

The invention belongs to the technical field of biological medicine, and particularly relates to a culture method and application of a hematological malignant tumor organoid. The culture method comprises the following steps: S01, obtaining a tumor cell sample; s02, preparing a bone marrow microenvironment simulation matrix, and resuspending tumor cells; s03, a specific culture medium is added for hematoma organoid culture; s04, performing phenotype identification on the cultured hematological malignant tumor organoid; and hematological malignant tumor organs with phenotypes close to those of bone marrow cells of the patient are screened out. According to the method system disclosed by the invention, the hematoma organoid is successfully cultured and is further subjected to phenotype identification, and the screened hematoma organoid is close to the cellular immune phenotype of a patient and can be used for accurate detection of clinical patient drug sensitivity and effective test of potential effective target drugs.

The invention provides a human interleukin 2-polyethylene glycol conjugate and use thereof. The human interleukin 2-polyethylene glycol conjugate provided by the invention comprises a recombinant human interleukin 2 containing at least one unnatural amino acid and PEG coupled to the at least one unnatural amino acid. The unnatural amino acid is a compound containing a carbonyl terminal group and having a structure as shown in formula (I) or an enantiomer thereof, and the PEG is coupled to the at least one unnatural amino acid by forming an oxime bond between the carbonyl terminal group and the PEG containing a hydroxylamine terminal group. The human interleukin 2-polyethylene glycol conjugate provided by the invention can be used individually or in combination with other anti-tumor drugs for the treatment of diseases such as solid tumors and hematologic tumors.

The invention relates to the technical field of biological detection, in particular to a biomarker for predicting or diagnosing a Selanisol inhibitor and application of the biomarker. The invention relates to an application of a substance for detecting the expression quantity of a gene. The application comprises an application in a product for predicting or diagnosing the drug resistance of Selanisole, an application in a product for screening or preparing a cancer targeted drug, and an application in a product for predicting the prognosis of a cancer patient. The invention also provides a pharmaceutical composition for treating the drug resistance of the Selanisole. Aiming at the drug resistance of the XPO1 inhibitor, the invention provides a brand new prediction, diagnosis and treatment method.

The invention relates to the field of medical auxiliary instruments, in particular to a hematologic tumor sample transfer box which comprises a box body, a partition plate capable of sliding up and down is arranged in the box body, a fixing assembly is arranged in the box body, and the fixing assembly comprises a first fixing frame, a second fixing frame and a connecting piece which are fixed to the bottom wall in the box body. The first fixing frame is used for limiting one side of the test tube rack; the second fixing frame is arranged in the box body and can slide horizontally; the second fixing frame corresponds to the first fixing frame and is used for limiting the other side of the test tube rack; a connecting piece is arranged between the partition plate and the second fixing frame, and when the partition plate slides upwards, the connecting piece pulls the second fixing frame back into the box body. A springback piece is arranged on one side of the second fixing frame, and when the partition plate resets downwards, the springback piece pops out the second fixing frame; the test tube rack for placing test tube samples can be integrally transferred into the box body and can be automatically locked, so that not only can quick transfer be realized, but also collision damage in the transfer process can be avoided.

Disclosed are Schistosoma japonicum eggs and the ingredients of secretions and excretions thereof, comprising eggs, egg culture supernatant, and egg secreted proteins. (hereinafter referred to as “Schistosoma eggs and secretions and excretions thereof” for short). A Schistosoma infection can significantly inhibit metastatic tumors of organs such as lungs, and an anti-tumor effect is mediated by the “Schistosoma eggs and secretions and excretions thereof”, which have the effect of inhibiting various host tumors, comprising lung cancer, liver cancer, melanoma, and hematological tumors. Two egg secreted proteins having an anti-tumor effect are further identified. The “Schistosoma eggs and secretions and excretions thereof” exert an anti-tumor effect by activating natural immunity such as alveolar macrophages. The “Schistosoma eggs and secretions and excretions thereof” have a potential application value in prevention and treatment of tumors in humans.

The invention discloses a hematologic tumor diagnosis and treatment primer group, a kit and application. The primer group comprises a first primer group and / or a second primer group, the first primer group is used for amplifying IGH, IGDH, IGK and IGL; the first primer group is used for amplifying TRB V-J, TRB D-J, TRG and TRD, the second primer group is used for amplifying TRB V-J, TRB D-J, TRG and TRD, after the primer groups amplify and rearrange sequences, the positive detection of clinical samples can be remarkably improved, the obtained CDR3 sequence can be used for clinical monitoring and can independently evaluate an immune group library of each patient, the immune state of an individual can be accurately reflected, the change condition of tumor cells of the patient can be dynamically monitored, and the clinical detection efficiency can be improved. And the method has good reliability and repeatability.

The present invention provides a transgenic cell and its application. The transgenic cell expresses a chimeric antigen receptor and a chemokine receptor, and the chemokine receptor includes CXCR2 and CXCR6. The transgenic cell can simultaneously express and secrete the chimeric antigen receptor and the chemokine receptor, enabling the transgenic cell to target tumor antigens, improving the ability of CAR-lymphocytes to infiltrate into solid tumors, enhancing the anti-tumor activity of CAR lymphocytes at the same time, and being applied to the treatment of solid tumors and hematological tumors.

The utility model relates to the technical field of blood sample sampling for hematologic tumor experiments, and discloses a blood sample sampling device based on hematologic tumor experiments, which comprises an experiment table, a temporary placing rack is fixedly mounted on one side of the top surface of the experiment table, and a test tube placing table is fixedly mounted in the middle of the top surface of the experiment table. A sterile operation assembly covers the outside of the test tube placement table, a storage cabinet is fixedly connected to the bottom of the experiment table, a separation ventilation plate is fixedly mounted in the middle of the inner side wall of the storage cabinet, and a ventilation fence is fixedly mounted on one side of the interior of the storage cabinet. According to the blood sample sampling device for the hematologic tumor experiment, through the arrangement of the sterile operation assembly, during experimental sampling, an operator samples blood through an operation hole and by wearing a silica gel glove, so that external dust and bacteria are isolated outside a transparent glass cover, and the operation of blood sample sampling in a sterile environment is realized; therefore, the blood sample cannot be polluted during sampling.

The present disclosure provides a group of aromatic (e.g., pyridinyl, pyrimidinyl, pyrazinyl, or phenyl) diamidine analogs and pharmaceutically acceptable salts that are useful for treating a proliferative disease. The proliferative disease may include solid cancer or blood cancer. Compositions, methods of synthesizing the same and methods for treating various cancer using the analogs are disclosed herein. The present disclosure also provides pharmaceutical formulations comprising at least one of the compounds with a pharmaceutically acceptable carrier, diluent or excipient therefor.

The present invention provides therapeutic, diagnostic, and prognostic methods for cancer. The invention provides methods of treating a cancer, methods of determining whether an individual having a cancer is likely to respond to a treatment including an immune checkpoint inhibitor (e.g., a PD-L1 axis binding antagonist), methods of predicting responsiveness of an individual having a cancer to a treatment including an immune checkpoint inhibitor (e.g., a PD-L1 axis binding antagonist), methods of selecting a therapy for an individual having a cancer, methods of providing a prognosis for an individual having a cancer, and methods of monitoring a response of an individual having a cancer, based on a blood tumor mutational burden (bTMB) score or a maximum somatic allele frequency (MSAF) from a sample (e.g., a whole blood sample, a plasma sample, a serum sample, or a combination thereof) from the individual.

The invention relates to the technical field of image recognition, and particularly discloses an auxiliary blood tumor pathological diagnosis system and method based on artificial intelligence, and the system extracts a pathological image group of a patient through a pathological diagnosis auxiliary platform, analyzes the data of each pathological image, and judges the effective feature value of each pathological image; the effective feature values of the pathological images are compared with a predefined effective feature threshold value to obtain a comparison result, and the pathological diagnosis auxiliary platform judges whether the effective features of the pathological images are enhanced or not based on the comparison result; and extracting cell characteristic data in each pathological image according to each pathological image, judging the characteristic complexity of each pathological image, and performing difference analysis on the pathological image group to complete auxiliary blood tumor pathological diagnosis.

The invention relates to the technical field of biological medicine, in particular to an NK cell and application of the NK cell in tumor treatment medicines.The NK cell is prepared through the following method that a, an anti-PD-L1 antibody with the concentration being 20-35 micrograms / mL is used for pretreating a human peripheral blood mononuclear cell; b, in a container coated with the anti-CD16 antibody, a culture medium containing Galunissertib is used for culture, and the concentration of the Galunissertib is 4-6 [mu] M; and step c, transforming and expressing an F158V mutant CD16a receptor of UniProt P08637 through gene engineering. According to the technical scheme, a systematic solution is provided for NK cell therapy of a targeted tumor microenvironment, and wider clinical application in treatment of solid tumors and hematological tumors is expected to be achieved.

The present invention relates to therapeutic treatment of cancer, particularly solid and hematological tumors, with combination therapy using PM14 and a topoisomerase I inhibitor.

The present disclosure provides methods and systems for genomic data representation and estimation of various biomarkers of interest in personalized medicine and particularly in cancer genomics such as molecular residual disease (MRD), tumor fraction (TF), blood tumor mutational burden (bTMB) and clonal hematopoiesis of indeterminate potential (ChIP).

The invention relates to the technical field of tumor examination management, and discloses a blood tumor identification early warning management system based on artificial intelligence, which comprises a switch for providing a hardware support layer, monitoring equipment and wireless equipment, the data storage module, the data acquisition module, the data analysis module, the examination early warning module, the management module, the clinical decision module and the user interface layer are used for examination management. And the data acquisition module is used for acquiring laboratory detection data, iconography examination data and symptom and sign data and feeding back the acquired data to the data analysis module. According to the method, the judgment of triggering early warning is performed on the patient by adopting the multi-modal detection indexes, so that potential patients with hematologic tumors can be identified at the first time, the misdiagnosis risk is reduced, and the effects of timely warning, early diagnosis and early treatment are achieved.

The present invention provides a method and system for early screening of hematologic malignancies based on multi-channel blood scattergrams. The method comprises: obtaining a blood scattergram of a target subject; inputting each of the blood scattergrams into a pre-constructed feature extraction network to obtain deep feature maps output by the feature extraction network corresponding to each of the blood scattergrams; inputting each of the obtained deep feature maps into a pre-trained balanced optimization model to obtain an enhanced feature map output by the balanced optimization model; inputting each of the enhanced feature maps into a pre-trained classifier to obtain a category prediction result output by the classifier; fusing each of the enhanced feature maps to obtain a fused feature map, and obtaining a fused feature category prediction result based on the fused feature map, and obtaining a final category prediction result through weighted calculation. This method implements computer-assisted screening, reduces the empirical dependence of early screening for hematologic malignancies, and improves the accuracy and efficiency of screening results.

The invention provides pyrazolotriazine and pyrazolopyrimidine derivatives as well as a preparation method, a pharmaceutical composition and application thereof. Specifically, the invention provides pyrazolo [1, 5-a] [1, 3, 5] triazine and pyrazolo [1, 5-a] pyrimidine derivatives as shown in a general formula (I) and / or pharmaceutically acceptable salts thereof, pharmaceutical compositions thereof and application of the derivatives as pharmaceutical active agents in drugs for preventing and / or treating diseases related to abnormal activity of CDKs, it is indicated that the compound has a good cell proliferation inhibition effect on solid tumors and hematologic tumors, and potential for treating related cancers and autoimmune diseases is achieved. # imgabs0 #

The invention provides an extraction method of high-performance gamma delta T immune cells and application of the high-performance gamma delta T immune cells in tumors. The method comprises the following steps: firstly, separating mononuclear cells from peripheral blood, carrying out activation induction by using a serum-free culture medium containing zoledronic acid, IL-15 and OKT3, and supplementing a culture medium containing IL-2 according to a specific proportion for multiplication culture from the third day of culture. Through the optimization process, the expression rate of TCR-gamma delta < + > is as high as 96.84%, and gamma delta T cells with high activity are obtained. An in-vivo tumor inhibition experiment shows that the cell has a remarkable growth inhibition effect on liver cancer nude mouse transplanted tumor, the effect is equivalent to that of a positive control drug, and obvious toxic and side effects are not observed. The method is stable in process and clear in component, and a reliable technical basis is provided for clinical transformation of gamma delta T cells in immunotherapy of solid tumors and hematologic tumors.

This invention belongs to the fields of medicinal chemistry and pharmaceutical technology, and relates to 1,4-benzodiazepines and their use in the preparation of antitumor drugs, specifically the use of 1,4-benzodiazepines in the preparation of annexin A3 (ANXA3) degrading agents and in the preparation of drugs for treating cancer. In particular, it discloses the use of 1,4-benzodiazepines, or pharmaceutically acceptable salts thereof, or stereoisomers thereof, or compositions of drugs with these as active ingredients, in the preparation of drugs for the prevention and treatment of tumors. These compounds can bind to the ANXA3 protein, induce ANXA3 protein degradation, inhibit the proliferation, cloning, migration, and invasion of tumor cells, and exert antitumor therapeutic effects in vivo. They can be used to treat solid tumors and hematological malignancies, including breast cancer, cervical cancer, ovarian cancer, colorectal cancer, gastric cancer, pancreatic cancer, lung cancer, esophageal cancer, liver cancer, leukemia, and melanoma.

The present application relates to the technical field of medical devices, in particular to a wound debridement device for blood tumor patients, comprising a handle vertically arranged, an injection part, an adsorption part and a mounting part for clamping medical cotton, the lower end of the handle is provided with a placing cavity, the mounting part is arranged in the placing cavity, the injection part comprises a first cylindrical cavity, a first button, a vertical slide and a first flow channel arranged in the handle, the mounting part comprises a fixing block arranged in the placing cavity and detachably connected with the handle, when the medical cotton is clamped on the handle by the fixing block, part of the medical cotton extends out of the lower end of the handle through the center hole of the fixing block, and the adsorption part comprises a second cylindrical cavity, a second button and an adsorption channel arranged vertically. The present application is simple and fast in operation when debriding the wound of the patient, greatly shortens the debridement time and reduces the labor intensity of medical staff, simultaneously reduces the time of exposing the wound of the patient to the outside, reduces the risk of wound infection and improves the wound healing speed.