<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12(2)</volume><submitter>Roex G</submitter><pubmed_abstract>Chimeric antigen receptor (CAR)-T-cell therapy is an innovative form of adoptive cell therapy that has revolutionized the treatment of certain hematological malignancies, including B-cell non-Hodgkin lymphoma (NHL) and B-cell acute lymphoblastic leukemia (ALL). The treatment is currently also being studied in other B-cell neoplasms, including multiple myeloma (MM) and chronic lymphocytic leukemia (CLL). CD19 and B-cell maturation antigen (BCMA) have been the most popular target antigens for CAR-T-cell immunotherapy of these malignancies. This review will discuss the efficacy and toxicity data from the pivotal clinical studies of CD19- and BCMA-targeted CAR-T-cell therapies in relapsed/refractory B-cell malignancies (NHL, ALL, CLL) and MM, respectively.</pubmed_abstract><journal>Pharmaceutics</journal><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7076393</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Chimeric Antigen Receptor-T-Cell Therapy for B-Cell Hematological Malignancies: An Update of the Pivotal Clinical Trial Data.</pubmed_title><pmcid>PMC7076393</pmcid><pubmed_authors>Lewalle P</pubmed_authors><pubmed_authors>Feys T</pubmed_authors><pubmed_authors>Beguin Y</pubmed_authors><pubmed_authors>Kerre T</pubmed_authors><pubmed_authors>Bron D</pubmed_authors><pubmed_authors>Anguille S</pubmed_authors><pubmed_authors>Poire X</pubmed_authors><pubmed_authors>Roex G</pubmed_authors><pubmed_authors>Vandenberghe P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Chimeric Antigen Receptor-T-Cell Therapy for B-Cell Hematological Malignancies: An Update of the Pivotal Clinical Trial Data.</name><description>Chimeric antigen receptor (CAR)-T-cell therapy is an innovative form of adoptive cell therapy that has revolutionized the treatment of certain hematological malignancies, including B-cell non-Hodgkin lymphoma (NHL) and B-cell acute lymphoblastic leukemia (ALL). The treatment is currently also being studied in other B-cell neoplasms, including multiple myeloma (MM) and chronic lymphocytic leukemia (CLL). CD19 and B-cell maturation antigen (BCMA) have been the most popular target antigens for CAR-T-cell immunotherapy of these malignancies. This review will discuss the efficacy and toxicity data from the pivotal clinical studies of CD19- and BCMA-targeted CAR-T-cell therapies in relapsed/refractory B-cell malignancies (NHL, ALL, CLL) and MM, respectively.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Feb</publication><modification>2020-11-19T12:34:39Z</modification><creation>2020-05-22T14:09:22Z</creation></dates><accession>S-EPMC7076393</accession><cross_references><pubmed>32102267</pubmed><doi>10.3390/pharmaceutics12020194</doi></cross_references></HashMap>