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Checkpoint inhibitor-based salvage regimens prior to autologous stem cell transplant improve event-free survival in relapsed/refractory classic Hodgkin lymphoma.
Desai, Sanjal H; Spinner, Michael A; David, Kevin; Bachanova, Veronika; Goyal, Gaurav; Kahl, Brad; Dorritie, Kathleen; Azzi, Jacques; Kenkre, Vaishalee P; Arai, Sally; Chang, Cheryl; Fusco, Brendon; Sumransub, Nuttavut; Hatic, Haris; Saba, Raya; Ibrahim, Uroosa; Harris, Elyse I; Shah, Harsh; Murphy, Jacob; Ansell, Stephen; Jagadish, Deepa; Orellana-Noia, Victor; Diefenbach, Catherine; Iyenger, Siddharth; Rappazzo, K C; Mishra, Rahul; Choi, Yun; Nowakowski, Grzegorz S; Advani, Ranjana H; Micallef, Ivana N.
Afiliación
  • Desai SH; Division of Hematology, Mayo Clinic, Rochester, Minnesota, USA.
  • Spinner MA; Division of Hematology, Oncology and Transplantation, University of Minnesota, Minneapolis, USA.
  • David K; Division of Oncology, Department of Medicine, Stanford University Medical Center, Stanford, California, USA.
  • Bachanova V; Department of Hematology and Medical Oncology, Rutgers Cancer Institute of New Jersey, New Brunswick, New Jersey, USA.
  • Goyal G; Division of Hematology, Oncology and Transplantation, University of Minnesota, Minneapolis, USA.
  • Kahl B; Division of Hematology, Oncology and Transplantation, Department of Medicine, University of Minnesota, Minneapolis, Minnesota, USA.
  • Dorritie K; O'Neal Comprehensive Cancer Center, University of Alabama, Birmingham, Alabama, USA.
  • Azzi J; Division of Hematology and Oncology, Washington University School of Medicine, St. Louis, Missouri, USA.
  • Kenkre VP; Division of Hematology-Oncology, UPMC Hillman Cancer Center, Pittsburgh, Pennsylvania, USA.
  • Arai S; Division of Hematology and Medical Oncology, Icahn School of Medicine Mount Sinai, New York, New York, USA.
  • Chang C; Department of Hematology, University of Wisconsin, Madison, Wisconsin, USA.
  • Fusco B; Division of Oncology, Department of Medicine, Stanford University Medical Center, Stanford, California, USA.
  • Sumransub N; Division of Oncology, Department of Medicine, Stanford University Medical Center, Stanford, California, USA.
  • Hatic H; Department of Hematology and Medical Oncology, Rutgers Cancer Institute of New Jersey, New Brunswick, New Jersey, USA.
  • Saba R; Division of Hematology, Oncology and Transplantation, University of Minnesota, Minneapolis, USA.
  • Ibrahim U; Division of Hematology, Oncology and Transplantation, Department of Medicine, University of Minnesota, Minneapolis, Minnesota, USA.
  • Harris EI; O'Neal Comprehensive Cancer Center, University of Alabama, Birmingham, Alabama, USA.
  • Shah H; Division of Hematology and Oncology, Washington University School of Medicine, St. Louis, Missouri, USA.
  • Murphy J; Division of Hematology and Medical Oncology, Icahn School of Medicine Mount Sinai, New York, New York, USA.
  • Ansell S; Department of Hematology, University of Wisconsin, Madison, Wisconsin, USA.
  • Jagadish D; Division of Hematology, Huntsman Cancer Institute, University of Utah, Salt Lake City, Utah, USA.
  • Orellana-Noia V; Department of Oncology, the Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore, Maryland, USA.
  • Diefenbach C; Division of Hematology, Mayo Clinic, Rochester, Minnesota, USA.
  • Iyenger S; Cleveland Clinic Foundation, Cleveland, Ohio, USA.
  • Rappazzo KC; Division of Hematology and Medical Oncology, Winship Cancer Institute, Emory University, Atlanta, Georgia, USA.
  • Mishra R; Perlmutter Cancer Center, NYU Grossman Medical School, New York, New York, USA.
  • Choi Y; Division of Hematology, Huntsman Cancer Institute, University of Utah, Salt Lake City, Utah, USA.
  • Nowakowski GS; Department of Oncology, the Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore, Maryland, USA.
  • Advani RH; Cleveland Clinic Foundation, Cleveland, Ohio, USA.
  • Micallef IN; Perlmutter Cancer Center, NYU Grossman Medical School, New York, New York, USA.
Am J Hematol ; 98(3): 464-471, 2023 03.
Article en En | MEDLINE | ID: mdl-36629030
ABSTRACT
Clinical trials of novel salvage therapies have encouraging outcomes for relapsed/refractory transplant-eligible classic Hodgkin lymphoma (R/R cHL) but comparison with conventional chemotherapy is lacking. Herein, we report the final analysis of a multicenter retrospective cohort of R/R cHL assessing outcomes by type of salvage therapy before autologous stem cell transplant (ASCT). R/R cHL patients who underwent ASCT at 14 institutions across the United States were included. Outcomes were compared among patients receiving conventional chemotherapy, brentuximab vedotin (BV) + chemotherapy, BV alone, and a checkpoint inhibitor (CPI)-based regimens before ASCT. Study endpoints included event-free survival (EFS), progression-free survival (PFS), and overall survival (OS). All endpoints are defined from relapse. Of 936 patients, 728 received conventional chemotherapy, 73 received BV + chemotherapy, 70 received BV alone, and 65 received CPI-based regimens prior to ASCT. When adjusted for time to relapse, pre-ASCT response and use of BV maintenance, patients receiving CPI-based regimens had superior 2-year EFS compared to conventional chemotherapy, BV + chemotherapy, and BV alone (79.7, 49.6, 62.3, and 36.9%, respectively, p < .0001). Among 649 patients transplanted after 1 line of salvage therapy, CPI-based regimens were associated with superior 2-year PFS compared to conventional chemotherapy (98% vs. 68.8%, hazard ratio 0.1, 95% confidence interval 0.03-0.5, p < .0001). OS did not differ by pre-ASCT salvage regimen. In this large multicenter retrospective study, CPI-based regimens improved EFS and PFS compared to other salvage regimens independent of pre-ASCT response. These data support earlier sequencing of CPI-based regimens in R/R cHL in the pre-ASCT setting.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Enfermedad de Hodgkin / Trasplante de Células Madre Hematopoyéticas Tipo de estudio: Clinical_trials / Observational_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Am J Hematol Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Enfermedad de Hodgkin / Trasplante de Células Madre Hematopoyéticas Tipo de estudio: Clinical_trials / Observational_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Am J Hematol Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos