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      Matched unrelated donor allogeneic transplantation provides comparable long-term outcome to HLA-identical sibling transplantation in relapsed diffuse large B-cell lymphoma.

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          Abstract

          The objective of this retrospective analysis was to compare outcomes of patients with diffuse large B-cell lymphoma (DLBCL) who received either a matched sibling (sib) or an unrelated donor (URD) allogeneic hematopoietic cell transplantation (allo-HCT). Long-term outcome of 172 DLBCL patients receiving URD-HCT between 2000 and 2007 and reported to the European Group for Blood and Marrow Transplantation, was compared with that of 301 subjects, allografted from sib-HCT. With a median follow-up of 45 months, 3-year PFS approached 35% for both groups; overall survival (OS) was 42% for sib-HCT versus 37% for URD (NS). Multivariate analyses confirmed that donor type was not associated with differences in non-relapse mortality (NRM), relapse rate (RR), PFS or OS. Poor performance status (PS) and refractory disease adversely affected PFS and OS. Prior auto-SCT and multiple previous therapies predicted for shorter PFS. NRM was adversely affected by older age (⩾50 years), poor PS and refractory disease, and RR by time from diagnosis to allo-HCT of <36 months, prior auto-SCT, refractory disease, poor PS and in vivo T-cell depletion with alemtuzumab. This large study shows for the first time that URD-HCT is not inferior to sib-HCT, providing a reasonable therapeutic approach for DLBCL patients, having no HLA-identical sibling available.

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          Author and article information

          Journal
          Bone Marrow Transplant.
          Bone marrow transplantation
          1476-5365
          0268-3369
          May 2014
          : 49
          : 5
          Affiliations
          [1 ] Department of Hematology & Bone Marrow Transplantation, Ramban Medical Center, Haifa, Israel.
          [2 ] Clinical Hematology Division, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
          [3 ] Clinical Hematology, Hopital Pitie Salpetriere, Paris, France.
          [4 ] Abteilung Hematologie und Onkologie, Universitätsklinikum Göttingen, Gottingen, Germany.
          [5 ] Department of Hematology & Bone Marrow Transplantation, Chaim Sheba Medical Center, Tel-Hashomer, Israel.
          [6 ] Service Hematologie Adulte, Hôpital Necker, Paris, France.
          [7 ] Department of Haematology, University Medical Centre, Utrecht, The Netherlands.
          [8 ] Service de Maladies du Sang, Hopital Claude Huriez, Lille, France.
          [9 ] Centre for Clinical Haematology, Queen Elizabeth Hospital, Birmingham, UK.
          [10 ] Department of Hematology, Radboud University-Nijmegen Medical Centre, Nijmegen, The Netherlands.
          [11 ] Division of Hematology, Oncology and Hemostasiology, University Hospital Leipzig, Leipzig, Germany.
          [12 ] Department of Haematology, University College London Hospital, London, UK.
          [13 ] Unit de Transplantation et de Therapie Cellulaire, Institut Paoli Calmettes, Marseille, France.
          [14 ] CHU Dept. Hematologie, Hopital de Purpan, Toulouse, France.
          [15 ] BMT Unit, Department of Internal Medicine, University of Saarland, Saarbrucken, Germany.
          [16 ] Department of Hematology, University Hospital, Basel, Switzerland.
          [17 ] Department of Hematology, Nottingham City Hospital, Nottingham, UK.
          [18 ] Medizinische Klinik u. Poliklinik V, University of Heidelberg, Heidelberg, Germany.
          [19 ] Department of Haematology, Addenbrookes Hospital, Cambridge University, Cambridge, UK.
          Article
          bmt20144
          10.1038/bmt.2014.4
          24510071
          51d9e619-0f95-4918-adff-61451347cf1d
          History

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