Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/125705
Title: Reduced-intensity Transplantation For Lymphomas Using Haploidentical Related Donors Versus Hla-matched Sibling Donors: A Center For International Blood And Marrow Transplant Research Analysis
Author: Ghosh, Nilanjan
Karmali, Reem
Rocha, Vanderson
Ahn, Kwang Woo
Digilio, Alyssa
Hari, Parameswaran
Bachanova, Veronika
Bacher, Ulrike
Dahi, Parastoo B.
Lima, Marcos de
D'Souza, Anita
Fenske, Timothy S.
Ganguly, Siddhartha
Kharfan-Dabaja, Mohamed A.
Prestidge, Tim D.
Savani, Bipin N.
Smith, Sonali M.
Sureda, Anna
Waller, Edmund K.
Jaglowski, Samantha
Herrera, Alex F.
Armand, Philippe
Salit, Rachel B.
Wagner-Johnston, Nina D.
Fuchs, Ephraim
Bolanos-Meade, Javier
Hamadani, Mehdi
Keywords: Limfomes
Ciclofosfamida
Lymphomas
Cyclophosphamide
Issue Date: 10-Sep-2016
Publisher: American Society of Clinical Oncology
Abstract: Purpose: Related donor haploidentical hematopoietic cell transplantation (Haplo-HCT) using post-transplantation cyclophosphamide (PT-Cy) is increasingly used in patients lacking HLA-matched sibling donors (MSD). We compared outcomes after Haplo-HCT using PT-Cy with MSD-HCT in patients with lymphoma, using the Center for International Blood and Marrow Transplant Research registry. Materials and Methods: We evaluated 987 adult patients undergoing either Haplo-HCT (n = 180) or MSD-HCT (n = 807) following reduced-intensity conditioning regimens. The haploidentical group received graft-versus-host disease (GVHD) prophylaxis with PT-Cy with or without a calcineurin inhibitor and mycophenolate. The MSD group received calcineurin inhibitor-based GVHD prophylaxis. Results: Median follow-up of survivors was 3 years. The 28-day neutrophil recovery was similar in the two groups (95% v 97%; P = .31). The 28-day platelet recovery was delayed in the haploidentical group compared with the MSD group (63% v 91%; P = .001). Cumulative incidence of grade II to IV acute GVHD at day 100 was similar between the two groups (27% v 25%; P = .84). Cumulative incidence of chronic GVHD at 1 year was significantly lower after Haplo-HCT (12% v 45%; P < .001), and this benefit was confirmed on multivariate analysis (relative risk, 0.21; 95% CI, 0.14 to 0.31; P < .001). For Haplo-HCT v MSD-HCT, 3-year rates of nonrelapse mortality (15% v 13%; P = .41), relapse/progression (37% v 40%; P = .51), progression-free survival (48% v 48%; P = .96), and overall survival (61% v 62%; P = .82) were similar. Multivariate analysis showed no significant difference between Haplo-HCT and MSD-HCT in terms of nonrelapse mortality (P = .06), progression/relapse (P = .10), progression-free survival (P = .83), and overall survival (P = .34). Conclusion: Haplo-HCT with PT-Cy provides survival outcomes comparable to MSD-HCT, with a significantly lower risk of chronic GVHD.
Note: Reproducció del document publicat a: https://doi.org/10.1200/JCO.2015.66.3476
It is part of: Journal of Clinical Oncology, 2016, vol. 34, num. 26, Pp 3141-3149
URI: http://hdl.handle.net/2445/125705
Related resource: https://doi.org/10.1200/JCO.2015.66.3476
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

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