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PD-1 blockade for relapsed lymphoma post-allogeneic hematopoietic cell transplant: high response rate but frequent GVHD.
Haverkos, Bradley M; Abbott, Diana; Hamadani, Mehdi; Armand, Philippe; Flowers, Mary E; Merryman, Reid; Kamdar, Manali; Kanate, Abraham Sebastian; Saad, Ayman; Mehta, Amitkumar; Ganguly, Siddhartha; Fenske, Timothy S; Hari, Parameswaran; Lowsky, Robert; Andritsos, Leslie; Jagasia, Madan; Bashey, Asad; Brown, Stacey; Bachanova, Veronika; Stephens, Deborah; Mineishi, Shin; Nakamura, Ryotaro; Chen, Yi-Bin; Blazar, Bruce R; Gutman, Jonathan; Devine, Steven M.
Afiliação
  • Haverkos BM; Division of Hematology, University of Colorado School of Medicine, Denver, CO.
  • Abbott D; Division of Biostatistics, University of Colorado, Denver, CO.
  • Hamadani M; Division of Hematology and Oncology, Medical College of Wisconsin and Center for International Blood and Marrow Transplant Research, Milwaukee, WI.
  • Armand P; Division of Hematology, Dana-Farber Cancer Institute, Boston, MA.
  • Flowers ME; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
  • Merryman R; Division of Hematology, Dana-Farber Cancer Institute, Boston, MA.
  • Kamdar M; Division of Hematology, University of Colorado School of Medicine, Denver, CO.
  • Kanate AS; Osborn Hematopoietic Malignancy and Transplantation Program, West Virginia University, Morgantown, WV.
  • Saad A; Blood and Marrow Transplant Program, University of Alabama at Birmingham, Birmingham, AL.
  • Mehta A; Blood and Marrow Transplant Program, University of Alabama at Birmingham, Birmingham, AL.
  • Ganguly S; Division of Hematologic Malignancies and Cellular Therapeutics, University of Kansas Medical Center, Kansas City, KS.
  • Fenske TS; Division of Hematology and Oncology, Medical College of Wisconsin and Center for International Blood and Marrow Transplant Research, Milwaukee, WI.
  • Hari P; Division of Hematology and Oncology, Medical College of Wisconsin and Center for International Blood and Marrow Transplant Research, Milwaukee, WI.
  • Lowsky R; Division of Blood and Marrow Transplantation, Stanford University, Stanford, CA.
  • Andritsos L; Division of Hematology, The Ohio State University, Columbus, OH.
  • Jagasia M; Division of Hematology-Oncology, Vanderbilt University Medical Center, Nashville, TN.
  • Bashey A; Blood and Marrow Transplant Program, Northside Hospital, Atlanta, GA.
  • Brown S; Blood and Marrow Transplant Program, Northside Hospital, Atlanta, GA.
  • Bachanova V; Division of Hematology, Oncology and Transplantation, University of Minnesota, Minneapolis, MN.
  • Stephens D; Division of Hematology and Hematologic Malignancies, University of Utah, Salt Lake City, UT.
  • Mineishi S; Division of Hematology, Penn State Cancer Institute, Hershey, PA.
  • Nakamura R; Division of Hematology, City of Hope, Los Angeles, CA.
  • Chen YB; Massachusetts General Hospital, Boston, MA; and.
  • Blazar BR; Division of Pediatric Blood and Marrow Transplantation, University of Minnesota, Minneapolis, MN.
  • Gutman J; Division of Hematology, University of Colorado School of Medicine, Denver, CO.
  • Devine SM; Division of Hematology, The Ohio State University, Columbus, OH.
Blood ; 130(2): 221-228, 2017 07 13.
Article em En | MEDLINE | ID: mdl-28468799
ABSTRACT
Given the limited treatment options for relapsed lymphoma post-allogeneic hematopoietic cell transplantation (post-allo-HCT) and the success of programmed death 1 (PD-1) blockade in classical Hodgkin lymphoma (cHL) patients, anti-PD-1 monoclonal antibodies (mAbs) are increasingly being used off-label after allo-HCT. To characterize the safety and efficacy of PD-1 blockade in this setting, we conducted a multicenter retrospective analysis of 31 lymphoma patients receiving anti-PD-1 mAbs for relapse post-allo-HCT. Twenty-nine (94%) patients had cHL and 27 had ≥1 salvage therapy post-allo-HCT and prior to anti-PD-1 treatment. Median follow-up was 428 days (range, 133-833) after the first dose of anti-PD-1. Overall response rate was 77% (15 complete responses and 8 partial responses) in 30 evaluable patients. At last follow-up, 11 of 31 patients progressed and 21 of 31 (68%) remain alive, with 8 (26%) deaths related to new-onset graft-versus-host disease (GVHD) after anti-PD-1. Seventeen (55%) patients developed treatment-emergent GVHD after initiation of anti-PD-1 (6 acute, 4 overlap, and 7 chronic), with onset after a median of 1, 2, and 2 doses, respectively. GVHD severity was grade III-IV acute or severe chronic in 9 patients. Only 2 of these 17 patients achieved complete response to GVHD treatment, and 14 of 17 required ≥2 systemic therapies. In conclusion, PD-1 blockade in relapsed cHL allo-HCT patients appears to be highly efficacious but frequently complicated by rapid onset of severe and treatment-refractory GVHD. PD-1 blockade post-allo-HCT should be studied further but cannot be recommended for routine use outside of a clinical trial.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Hodgkin / Transplante de Células-Tronco Hematopoéticas / Anticorpos Monoclonais Humanizados / Receptor de Morte Celular Programada 1 / Doença Enxerto-Hospedeiro / Anticorpos Monoclonais Tipo de estudo: Observational_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Hodgkin / Transplante de Células-Tronco Hematopoéticas / Anticorpos Monoclonais Humanizados / Receptor de Morte Celular Programada 1 / Doença Enxerto-Hospedeiro / Anticorpos Monoclonais Tipo de estudo: Observational_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article