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A multicenter retrospective study of polatuzumab vedotin in patients with large B-cell lymphoma after CAR T-cell therapy.
Gouni, Sushanth; Rosenthal, Allison C; Crombie, Jennifer L; Ip, Andrew; Kamdar, Manali K; Hess, Brian; Feng, Lei; Watson, Grace; Ayers, Amy; Neelapu, Sattva S; Khurana, Arushi; Lin, Yi; Iqbal, Madiha; Merryman, Reid W; Strati, Paolo.
Afiliación
  • Gouni S; Department of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX.
  • Rosenthal AC; Division of Hematology-Oncology, Mayo Clinic, Phoenix, AZ.
  • Crombie JL; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
  • Ip A; John Theurer Cancer Center, Hackensack University Medical Center, Hackensack, NJ.
  • Kamdar MK; Blood Disorders Center, University of Colorado, Aurora, CO.
  • Hess B; Division of Haematology, Medical University of South Carolina, Charleston, SC.
  • Feng L; Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX.
  • Watson G; Department of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX.
  • Ayers A; Department of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX.
  • Neelapu SS; Department of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX.
  • Khurana A; Division of Hematology, Mayo Clinic, Rochester, MN; and.
  • Lin Y; Division of Hematology, Mayo Clinic, Rochester, MN; and.
  • Iqbal M; Division of Hematology, Mayo Clinic, Jacksonville, FL.
  • Merryman RW; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
  • Strati P; Department of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX.
Blood Adv ; 6(9): 2757-2762, 2022 05 10.
Article en En | MEDLINE | ID: mdl-35240681
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 = .003) and elevated lactate dehydrogenase levels (hazard ratio, 5.0; 95% CI, 1.4-16; P = .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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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Linfoma de Células B Grandes Difuso / Inmunoconjugados Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Blood Adv Año: 2022 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Linfoma de Células B Grandes Difuso / Inmunoconjugados Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Blood Adv Año: 2022 Tipo del documento: Article Pais de publicación: Estados Unidos