TY - JOUR
T1 - Top advances in lymphoma for 2021
AU - Patel, Dilan A.
AU - Kahl, Brad S.
N1 - Funding Information:
The authors would like to thank the Department of Medicine and Division of Oncology at the Washington University School of Medicine along with the patients, families, and research and support staff for contributing to the advancement of care. No funding sources were used.
Publisher Copyright:
© 2022 American Cancer Society.
PY - 2022
Y1 - 2022
N2 - Chimeric antigen receptor (CAR) T-cell therapy, antibody–drug conjugates, bispecific T-cell redirectors, and agents targeting tonic B-cell receptor signaling have altered the paradigm for three of the most common lymphomas in the year 2021. For diffuse large B-cell lymphoma, the POLARIX study has shown improvement on the standard backbone of rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone in the frontline setting, a feat that had not been achieved despite great efforts over the past 20 years. In the relapsed and refractory setting, two unique CAR T-cell products have displaced autologous transplantation to the third line, and they allow patients with chemotherapy-resistant disease to receive approved therapy earlier. CAR T-cell products, once used exclusively in the aggressive lymphoma arena, are now showing high response rates and durable activity against indolent lymphomas. The investigation of mosunetuzumab in indolent lymphomas offers another option for patients who have received multiple lines of cytotoxic drugs. On the basis of these trends, PI3K inhibitors are being displaced in favor of safer and more durable constructs. In addition, within the past year, the approval and implementation of zanubrutinib for marginal zone lymphoma have filled a need for later line therapy, especially for less fit and elderly patients.
AB - Chimeric antigen receptor (CAR) T-cell therapy, antibody–drug conjugates, bispecific T-cell redirectors, and agents targeting tonic B-cell receptor signaling have altered the paradigm for three of the most common lymphomas in the year 2021. For diffuse large B-cell lymphoma, the POLARIX study has shown improvement on the standard backbone of rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone in the frontline setting, a feat that had not been achieved despite great efforts over the past 20 years. In the relapsed and refractory setting, two unique CAR T-cell products have displaced autologous transplantation to the third line, and they allow patients with chemotherapy-resistant disease to receive approved therapy earlier. CAR T-cell products, once used exclusively in the aggressive lymphoma arena, are now showing high response rates and durable activity against indolent lymphomas. The investigation of mosunetuzumab in indolent lymphomas offers another option for patients who have received multiple lines of cytotoxic drugs. On the basis of these trends, PI3K inhibitors are being displaced in favor of safer and more durable constructs. In addition, within the past year, the approval and implementation of zanubrutinib for marginal zone lymphoma have filled a need for later line therapy, especially for less fit and elderly patients.
KW - BTK inhibitors
KW - CAR T-cell therapy
KW - Diffuse large B-cell lymphoma
KW - bispecific T-cell redirecting agents
KW - follicular lymphoma
KW - marginal zone lymphoma
UR - http://www.scopus.com/inward/record.url?scp=85139391220&partnerID=8YFLogxK
U2 - 10.1002/cncr.34483
DO - 10.1002/cncr.34483
M3 - Comment/debate
C2 - 36201139
AN - SCOPUS:85139391220
SN - 0008-543X
JO - Cancer
JF - Cancer
ER -