TY - JOUR
T1 - Post-transplantation cyclophosphamide versus antithymocyte globulin in patients with acute myeloid leukemia undergoing allogeneic stem cell transplantation from HLA-identical sibling donors
T2 - A retrospective analysis from the Acute Leukemia Working Party of the European Society for Blood and Marrow Transplantation
AU - Battipaglia, Giorgia
AU - Labopin, Myriam
AU - Hamladji, Rose Marie
AU - Blaise, Didier
AU - Chevallier, Patrice
AU - Brissot, Eolia
AU - Gerbitz, Armin
AU - Socié, Gerard
AU - Afanasyev, Boris
AU - Ciceri, Fabio
AU - Meijer, Ellen
AU - Koc, Yener
AU - Cornelissen, Jan J.
AU - Huynh, Anne
AU - Ozdogu, Hakan
AU - Maertens, Johan
AU - Paul, Franciane
AU - Labussière-Wallet, Hélène
AU - Ruggeri, Annalisa
AU - Aljurf, Mahmoud
AU - Bazarbachi, Ali
AU - Savani, Bipin
AU - Nagler, Arnon
AU - Mohty, Mohamad
N1 - Publisher Copyright:
© 2020 American Cancer Society
PY - 2021/1/15
Y1 - 2021/1/15
N2 - 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.
AB - 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.
KW - acute myeloid leukemia
KW - allogeneic hematopoietic transplantation
KW - antithymocyte globulin
KW - graft-versus-host disease
KW - post-transplantation cyclophosphamide
UR - http://www.scopus.com/inward/record.url?scp=85094193837&partnerID=8YFLogxK
U2 - 10.1002/cncr.33255
DO - 10.1002/cncr.33255
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C2 - 33119152
AN - SCOPUS:85094193837
SN - 0008-543X
VL - 127
SP - 209
EP - 218
JO - Cancer
JF - Cancer
IS - 2
ER -