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The graft-versus-leukemia effect using matched unrelated donors is not superior to HLA-identical siblings for hematopoietic stem cell transplantation

Ringden, O (author)
Karolinska Institutet
Pavletic, SZ (author)
Anasetti, C (author)
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Barrett, AJ (author)
Wang, T (author)
Wang, D (author)
Antin, JH (author)
Di Bartolomeo, P (author)
Bolwell, BJ (author)
Bredeson, C (author)
Cairo, MS (author)
Gale, RP (author)
Gupta, V (author)
Hahn, T (author)
Hale, GA (author)
Halter, J (author)
Jagasia, M (author)
Litzow, MR (author)
Locatelli, F (author)
Marks, DI (author)
McCarthy, PL (author)
Cowan, MJ (author)
Petersdorf, EW (author)
Russell, JA (author)
Schiller, GJ (author)
Schouten, H (author)
Spellman, S (author)
Verdonck, LF (author)
Wingard, JR (author)
Horowitz, MM (author)
Arora, M (author)
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 (creator_code:org_t)
American Society of Hematology, 2009
2009
English.
In: Blood. - : American Society of Hematology. - 1528-0020 .- 0006-4971. ; 113:13, s. 3110-3118
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Do some patients benefit from an unrelated donor (URD) transplant because of a stronger graft-versus-leukemia (GVL) effect? We analyzed 4099 patients with acute myeloid leukemia (AML), acute lymphoblastic leukemia (ALL), and chronic myeloid leukemia (CML) undergoing a myeloablative allogeneic hematopoietic cell transplantation (HCT) from an URD (8/8 human leukocyte antigen [HLA]–matched, n = 941) or HLA-identical sibling donor (n = 3158) between 1995 and 2004 reported to the CIBMTR. In the Cox regression model, acute and chronic GVHD were added as time-dependent variables. In multivariate analysis, URD transplant recipients had a higher risk for transplantation-related mortality (TRM; relative risk [RR], 2.76; P < .001) and relapse (RR, 1.50; P < .002) in patients with AML, but not ALL or CML. Chronic GVHD was associated with a lower relapse risk in all diagnoses. Leukemia-free survival (LFS) was decreased in patients with AML without acute GVHD receiving a URD transplant (RR, 2.02; P < .001) but was comparable to those receiving HLA-identical sibling transplants in patients with ALL and CML. In patients without GVHD, multivariate analysis showed similar risk of relapse but decreased LFS for URD transplants for all 3 diagnoses. In conclusion, risk of relapse was the same (ALL, CML) or worse (AML) in URD transplant recipients compared with HLA-identical sibling transplant recipients, suggesting a similar GVL effect.

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