TY - JOUR
T1 - Advances in chimeric antigen receptor T cells
AU - Beyar-Katz, Ofrat
AU - Gill, Saar
N1 - Publisher Copyright:
© 2020 Lippincott Williams and Wilkins. All rights reserved.
PY - 2020/11/1
Y1 - 2020/11/1
N2 - Purpose of reviewTo discuss the important advances in CAR T cell therapy over the past year, focusing on clinical results where available.Recent findingsApproximately 30 years after they were first conceived of and 15 years after the first small-scale single-center clinical trials, the past 3 years represent a major milestone in the development of CAR T cells. In the United States, the Food and Drug Administration (FDA) approved Tisagenlecleucel for the treatment of relapsed/refractory B-ALL and Axicabtagene Ciloleucel, for adults with relapsed/refractory diffuse large B cell lymphoma (R/R DLBCL) in 2017. Tisagenlecleucel received a second indication in adults with R/R DLBCL in 2018. Regulatory approval for CAR T cells was then granted in Europe, Canada, Australia, and Japan. Most recently, in July 2020 the FDA granted regulatory approval to a third CAR T cell product, Brexucabtagene Autoleucel for mantle cell lymphoma. All products target the CD19 antigen but differ in the costimulatory molecule within the CAR construct. Currently, it is unknown whether there are any differences in clinical activity or toxicity between these products.SummaryThe CAR T cell the platform is evolving at a rapid pace and is expected to further improve the therapeutic outcomes of hematological malignancies.
AB - Purpose of reviewTo discuss the important advances in CAR T cell therapy over the past year, focusing on clinical results where available.Recent findingsApproximately 30 years after they were first conceived of and 15 years after the first small-scale single-center clinical trials, the past 3 years represent a major milestone in the development of CAR T cells. In the United States, the Food and Drug Administration (FDA) approved Tisagenlecleucel for the treatment of relapsed/refractory B-ALL and Axicabtagene Ciloleucel, for adults with relapsed/refractory diffuse large B cell lymphoma (R/R DLBCL) in 2017. Tisagenlecleucel received a second indication in adults with R/R DLBCL in 2018. Regulatory approval for CAR T cells was then granted in Europe, Canada, Australia, and Japan. Most recently, in July 2020 the FDA granted regulatory approval to a third CAR T cell product, Brexucabtagene Autoleucel for mantle cell lymphoma. All products target the CD19 antigen but differ in the costimulatory molecule within the CAR construct. Currently, it is unknown whether there are any differences in clinical activity or toxicity between these products.SummaryThe CAR T cell the platform is evolving at a rapid pace and is expected to further improve the therapeutic outcomes of hematological malignancies.
KW - chimeric antigen receptor T cells
KW - leukemia
KW - lymphoma
KW - multiple myeloma
UR - http://www.scopus.com/inward/record.url?scp=85092682366&partnerID=8YFLogxK
U2 - 10.1097/MOH.0000000000000614
DO - 10.1097/MOH.0000000000000614
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C2 - 32925186
AN - SCOPUS:85092682366
SN - 1065-6251
VL - 27
SP - 368
EP - 377
JO - Current Opinion in Hematology
JF - Current Opinion in Hematology
IS - 6
ER -