TY - JOUR
T1 - A multicenter retrospective study of polatuzumab vedotin in patients with large B-cell lymphoma after CAR T-cell therapy
AU - Gouni, Sushanth
AU - Rosenthal, Allison C.
AU - Crombie, Jennifer L.
AU - Ip, Andrew
AU - Kamdar, Manali K.
AU - Hess, Brian
AU - Feng, Lei
AU - Watson, Grace
AU - Ayers, Amy
AU - Neelapu, Sattva S.
AU - Khurana, Arushi
AU - Lin, Yi
AU - Iqbal, Madiha
AU - Merryman, Reid W.
AU - Strati, Paolo
N1 - Funding Information:
This research was supported in part by The University of Texas Anderson Cancer Center Support Grant from the National Institutes of Health, National Cancer Institute (P30 CA016672), and by the Lymphoma Research Foundation Clinical Research Mentoring Program. The salary of P.S. is supported by the Lymphoma Research Foundation Career Development Award and by the R21 NIH grant.
Publisher Copyright:
© 2022 by The American Society of Hematology.
PY - 2022/5/10
Y1 - 2022/5/10
N2 - Polatuzumab vedotin (PV) is an antibody–drug conjugate targeting CD79b that is approved for patients with relapsed/refractory large B-cell lymphoma (LBCL). Patients who relapse after chimeric antigen receptor (CAR) T-cell therapy were not included in the registration study, and reports of PV use after CAR T cells are limited. This multicenter retrospective analysis included patients with LBCL who relapsed or progressed after CAR T-cell therapy and subsequently received PV with or without rituximab and bendamustine between July 2019 and May 2021. Response to treatment and progression were assessed based on the 2014 Lugano criteria. Fifty-seven patients were included in the study: 18 (32%) patients were primary refractory to CAR T-cell therapy, and 34 (60%) patients received PV-based therapy immediately after CAR T-cell therapy. PV was combined with rituximab in 54 (95%) patients and administered with bendamustine in 35 (61%) patients. A response was achieved in 25 (44%) patients, including complete remission in 8 (14%). No significant association between baseline characteristics and response was observed. After a median follow-up of 47 weeks (95% confidence interval [CI], 40-54), 46 (81%) patients had disease progression or died, and the median progression-free survival was 10 weeks (95% CI, 5-15). On a multivariate analysis, bone marrow involvement (hazard ratio, 5.2; 95% CI, 1.8-15; P 5 .003) and elevated lactate dehydrogenase levels (hazard ratio, 5.0; 95% CI, 1.4-16; P 5 .01) were associated with shorter progression-free survival. Studies aimed at better characterizing the intrinsic mechanism of resistance and identifying optimal consolidation strategies for these patients are warranted.
AB - Polatuzumab vedotin (PV) is an antibody–drug conjugate targeting CD79b that is approved for patients with relapsed/refractory large B-cell lymphoma (LBCL). Patients who relapse after chimeric antigen receptor (CAR) T-cell therapy were not included in the registration study, and reports of PV use after CAR T cells are limited. This multicenter retrospective analysis included patients with LBCL who relapsed or progressed after CAR T-cell therapy and subsequently received PV with or without rituximab and bendamustine between July 2019 and May 2021. Response to treatment and progression were assessed based on the 2014 Lugano criteria. Fifty-seven patients were included in the study: 18 (32%) patients were primary refractory to CAR T-cell therapy, and 34 (60%) patients received PV-based therapy immediately after CAR T-cell therapy. PV was combined with rituximab in 54 (95%) patients and administered with bendamustine in 35 (61%) patients. A response was achieved in 25 (44%) patients, including complete remission in 8 (14%). No significant association between baseline characteristics and response was observed. After a median follow-up of 47 weeks (95% confidence interval [CI], 40-54), 46 (81%) patients had disease progression or died, and the median progression-free survival was 10 weeks (95% CI, 5-15). On a multivariate analysis, bone marrow involvement (hazard ratio, 5.2; 95% CI, 1.8-15; P 5 .003) and elevated lactate dehydrogenase levels (hazard ratio, 5.0; 95% CI, 1.4-16; P 5 .01) were associated with shorter progression-free survival. Studies aimed at better characterizing the intrinsic mechanism of resistance and identifying optimal consolidation strategies for these patients are warranted.
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U2 - 10.1182/bloodadvances.2021006801
DO - 10.1182/bloodadvances.2021006801
M3 - Article
C2 - 35240681
AN - SCOPUS:85130205079
SN - 2473-9529
VL - 6
SP - 2757
EP - 2762
JO - Blood Advances
JF - Blood Advances
IS - 9
ER -