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Long-term survival outcomes of reduced-intensity allogeneic or autologous transplantation in relapsed grade 3 follicular lymphoma.
Klyuchnikov, E; Bacher, U; Woo Ahn, K; Carreras, J; Kröger, N M; Hari, P N; Ku, G H; Ayala, E; Chen, A I; Chen, Y-B; Cohen, J B; Freytes, C O; Gale, R P; Kamble, R T; Kharfan-Dabaja, M A; Lazarus, H M; Martino, R; Mussetti, A; Savani, B N; Schouten, H C; Usmani, S Z; Wiernik, P H; Wirk, B; Smith, S M; Sureda, A; Hamadani, M.
Afiliação
  • Klyuchnikov E; Department for Stem Cell Transplantation, University Cancer Center Hamburg, Hamburg, Germany.
  • Bacher U; Department for Hematology/Oncology, Georg August University Göttingen, Göttingen, Germany.
  • Woo Ahn K; CIBMTR (Center for International Blood and Marrow Transplant Research), Department of Medicine, Medical College of Wisconsin, Milwaukee, WI, USA.
  • Carreras J; Division of Biostatistics, Institute for Health and Society, Medical College of Wisconsin, Milwaukee, WI, USA.
  • Kröger NM; CIBMTR (Center for International Blood and Marrow Transplant Research), Department of Medicine, Medical College of Wisconsin, Milwaukee, WI, USA.
  • Hari PN; Department for Stem Cell Transplantation, University Cancer Center Hamburg, Hamburg, Germany.
  • Ku GH; CIBMTR (Center for International Blood and Marrow Transplant Research), Department of Medicine, Medical College of Wisconsin, Milwaukee, WI, USA.
  • Ayala E; Division of Blood and Marrow Transplantation, Department of Medicine, University of California, San Diego, CA, USA.
  • Chen AI; Department of Blood and Marrow Transplantation, H Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.
  • Chen YB; Oregon Health and Science University, Portland, OR, USA.
  • Cohen JB; Division of Hematology/Oncology, Massachusetts General Hospital, Boston, MA, USA.
  • Freytes CO; Department of Hematology and Medical Oncology, Winship Cancer Institute, Emory University School of Medicine, Atlanta, GA, USA.
  • Gale RP; South Texas Veterans Health Care System and University of Texas Health Science Center San Antonio, San Antonio, TX, USA.
  • Kamble RT; Hematology Research Centre, Division of Experimental Medicine, Department of Medicine, Imperial College of London, London, UK.
  • Kharfan-Dabaja MA; Division of Hematology and Oncology, Center for Cell and Gene Therapy, Baylor College of Medicine, Houston, TX, USA.
  • Lazarus HM; Department of Blood and Marrow Transplantation, H Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.
  • Martino R; Seidman Cancer Center, University Hospitals Case Medical Center, Cleveland, OH, USA.
  • Mussetti A; Division of Clinical Hematology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
  • Savani BN; SC Ematologia e Trapianto Midollo Osseo, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
  • Schouten HC; Università degli Studi di Milano, Milan, Italy.
  • Usmani SZ; Division of Hematology/Oncology, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
  • Wiernik PH; Department of Hematology, Academische Ziekenhuis, Maastricht, Netherlands.
  • Wirk B; Department of Hematology - Medical Oncology, Levine Cancer Institute, Carolinas HealthCare System, Charlotte, NC, USA.
  • Smith SM; Our Lady of Mercy Medical Center, Bronx, NY, USA.
  • Sureda A; Division of Bone Marrow Transplant, Seattle Cancer Care Alliance, Seattle, WA, USA.
  • Hamadani M; Section of Hematology/Oncology, The University of Chicago, Chicago, IL, USA.
Bone Marrow Transplant ; 51(1): 58-66, 2016 Jan.
Article em En | MEDLINE | ID: mdl-26437062
Grade 3 follicular lymphoma (FL) has aggressive clinical behavior. To evaluate the optimal first transplantation approach in relapsed/refractory grade 3 FL patients, we compared the long-term outcomes after allogeneic (allo-) vs autologous hematopoietic cell transplantation (auto-HCT) in the rituximab era. A total of 197 patients undergoing first reduced-intensity conditioning (RIC) allo-HCT or first auto-HCT during 2000-2012 were included. Rituximab-naive patients were excluded. Allo-HCT recipients were younger, more heavily pretreated and had a longer interval between diagnosis and HCT. The 5-year probabilities of non-relapse mortality (NRM), relapse/progression, PFS and overall survival (OS) for auto-HCT vs allo-HCT groups were 4% vs 27% (P<0.001), 61% vs 20% (P<0.001), 36% vs 51% (P=0.07) and 59% vs 54% (P=0.7), respectively. On multivariate analysis, auto-HCT was associated with reduced risk of NRM (relative risk (RR)=0.20; P=0.001). Within the first 11 months post HCT, auto- and allo-HCT had similar risks of relapse/progression and PFS. Beyond 11 months, auto-HCT was associated with higher risk of relapse/progression (RR=21.3; P=0.003) and inferior PFS (RR=3.2; P=0.005). In the first 24 months post HCT, auto-HCT was associated with improved OS (RR=0.42; P=0.005), but in long-time survivors (beyond 24 months) it was associated with inferior OS (RR=3.6; P=0.04). RIC allo-HCT as the first transplant approach can provide improved PFS and OS, in long-term survivors.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linfoma Folicular / Transplante de Células-Tronco Hematopoéticas Tipo de estudo: Clinical_trials / Etiology_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linfoma Folicular / Transplante de Células-Tronco Hematopoéticas Tipo de estudo: Clinical_trials / Etiology_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2016 Tipo de documento: Article