Abstract
BACKGROUND: Graft-versus-host disease (GVHD) is a major complication after allogeneic hematopoietic stem cell transplantation (allo-HSCT). Addition of antithymocyte globulin (ATG) or post-transplantation cyclophosphamide (PTCY) to standard immunosuppressive agents reduces GVHD in different donor settings. METHODS: We compared the outcomes of adults with acute myeloid leukemia undergoing allo-HSCT from HLA-identical sibling donors after the use of PTCY (n = 197) or ATG (n = 1913). RESULTS: Patients in the PTCY group were younger than those in the ATG group (median age, 47 vs 54 years; P <.01). Peripheral blood was the most frequently used stem cell source, being significantly more frequent in the ATG group than in the PTCY group (95% vs 70% P <.01). The conditioning regimen was more frequently myeloablative in the PTCY group than in the ATG group (59% vs 48%; P <.01). Time to neutrophil engraftment was shorter in the ATG group than in the PTCY group (17 vs 20 days; P <.01). No differences were observed according to the other transplantation outcomes, except for chronic GVHD of all grades and extensive chronic GVHD at 2 years, which were significantly lower in the ATG group compared with the PTCY group (P <.02). CONCLUSION: PTCY is feasible in an HLA-identical sibling setting, and despite similar outcomes, ATG may be associated with lower incidence of chronic GVHD.
Original language | English |
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Pages (from-to) | 209-218 |
Number of pages | 10 |
Journal | Cancer |
Volume | 127 |
Issue number | 2 |
DOIs | |
Publication status | Published - 15 Jan 2021 |
Bibliographical note
Funding Information:Johan Maertens has received grants from Gilead Sciences, Merck Sharp & Dohme, and Pfizer; personal fees from Gilead Sciences, Merck Sharp & Dohme, Pfizer, Mundipharma, Cidara, and F2G; and nonfinancial support from Gilead Sciences, Merck Sharp & Dohme, Pfizer, Mundipharma, Cidara, and F2G. Franciane Paul has received personal fees from Novartis. The other authors made no disclosures.
Publisher Copyright:
© 2020 American Cancer Society
Research programs
- EMC OR-01