
Chimeric antigen receptor T-cell (CAR T-cells) therapies which are genetically modified T lymphocyte targeting tumor antigens have modified therapeutic landscape in hematology. Aggressive B cells lymphoma are currently treated in daily practice with anti-CD19 CAR T. In indolent B cell lymphomas, their efficacy has been established by recent clinical trials. Longer follow-up evaluation is needed to determine their added value in a field where approved strategies already provide high long-term survival rates. They will also be challenged by another immunotherapy with bispecific antibodies. In chronic lymphoid leukemia, early phase trials have identified several limitations related to the immune context of this disease, but associations with targeted therapy like ibrutinib are very promising. In this moving therapeutic landscape, molecular and cellular engineering progress will increase the capacities of these new cellular-based therapies.
Lymphoma, B-Cell, Receptors, Chimeric Antigen, CAR T-cells, Immunothérapie, Adenine, T-Lymphocytes, Antigens, CD19, Leukemia, Lymphocytic, Chronic, B-Cell, [SDV] Life Sciences [q-bio], Cellules CAR-T, Clinical Trials, Phase II as Topic, LNH indolents, Piperidines, Antigens, Neoplasm, Antibodies, Bispecific, Humans, Immunotherapy, Genetic Engineering, Indolent NHL, Cell Engineering, CLL, LLC
Lymphoma, B-Cell, Receptors, Chimeric Antigen, CAR T-cells, Immunothérapie, Adenine, T-Lymphocytes, Antigens, CD19, Leukemia, Lymphocytic, Chronic, B-Cell, [SDV] Life Sciences [q-bio], Cellules CAR-T, Clinical Trials, Phase II as Topic, LNH indolents, Piperidines, Antigens, Neoplasm, Antibodies, Bispecific, Humans, Immunotherapy, Genetic Engineering, Indolent NHL, Cell Engineering, CLL, LLC
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