TY - JOUR
T1 - Risk factors for acute GVHD and survival after hematopoietic cell transplantation
AU - Jagasia, Madan
AU - Arora, Mukta
AU - Flowers, Mary E D
AU - Chao, Nelson J.
AU - McCarthy, Philip L.
AU - Cutler, Corey S.
AU - Urbano-Ispizua, Alvaro
AU - Pavletic, Steven Z.
AU - Haagenson, Michael D.
AU - Zhang, Mei Jie
AU - Antin, Joseph H.
AU - Bolwell, Brian J.
AU - Bredeson, Christopher
AU - Cahn, Jean Yves
AU - Cairo, Mitchell
AU - Gale, Robert Peter
AU - Gupta, Vikas
AU - Lee, Stephanie J.
AU - Litzow, Mark
AU - Weisdorf, Daniel J.
AU - Horowitz, Mary M.
AU - Hahn, Theresa
PY - 2012/1/5
Y1 - 2012/1/5
N2 - Risk factors for acute GVHD (AGVHD), overall survival, and transplant-related mortality were evaluated in adults receiving allogeneic hematopoietic cell transplants (1999-2005) from HLA-identical sibling donors (SDs; n = 3191) or unrelated donors (URDs; n = 2370) and reported to the Center for International Blood and Marrow Transplant Research, Minneapolis, MN. To understand the impact of transplant regimen onAGVHD risk, 6 treatment categories were evaluated: (1) myeloablative conditioning (MA) with total body irradiation (TBI) + PBSCs, (2) MA + TBI + BM, (3) MA + nonTBI + PB-SCs, (4) MA + nonTBI + BM, (5) reduced intensity conditioning (RIC) + PBSCs, and (6) RIC + BM. The cumulative incidences of grades B-D AGVHD were 39% (95% confidence interval [CI], 37%-41%) in the SD cohort and 59% (95% CI, 57%-61%) in the URD cohort. Patients receiving SD transplants with MA + nonTBI + BM and RIC + PBSCs had significantly lower risks of grades B-D AGVHD than patients in other treatment categories. Those receiving URD transplants with MA + TBI + BM, MA + nonTBI + BM, RIC + BM, or RIC + PB-SCs had lower risks of grades B-DAGVHD than those in other treatment categories. The 5-year probabilities of survival were 46% (95% CI, 44%-49%) with SD transplants and 33% (95% CI, 31%-35%) with URD transplants. Conditioning intensity, TBI and graft source have a combined effect on risk of AGVHD that must be considered in deciding on a treatment strategy for individual patients.
AB - Risk factors for acute GVHD (AGVHD), overall survival, and transplant-related mortality were evaluated in adults receiving allogeneic hematopoietic cell transplants (1999-2005) from HLA-identical sibling donors (SDs; n = 3191) or unrelated donors (URDs; n = 2370) and reported to the Center for International Blood and Marrow Transplant Research, Minneapolis, MN. To understand the impact of transplant regimen onAGVHD risk, 6 treatment categories were evaluated: (1) myeloablative conditioning (MA) with total body irradiation (TBI) + PBSCs, (2) MA + TBI + BM, (3) MA + nonTBI + PB-SCs, (4) MA + nonTBI + BM, (5) reduced intensity conditioning (RIC) + PBSCs, and (6) RIC + BM. The cumulative incidences of grades B-D AGVHD were 39% (95% confidence interval [CI], 37%-41%) in the SD cohort and 59% (95% CI, 57%-61%) in the URD cohort. Patients receiving SD transplants with MA + nonTBI + BM and RIC + PBSCs had significantly lower risks of grades B-D AGVHD than patients in other treatment categories. Those receiving URD transplants with MA + TBI + BM, MA + nonTBI + BM, RIC + BM, or RIC + PB-SCs had lower risks of grades B-DAGVHD than those in other treatment categories. The 5-year probabilities of survival were 46% (95% CI, 44%-49%) with SD transplants and 33% (95% CI, 31%-35%) with URD transplants. Conditioning intensity, TBI and graft source have a combined effect on risk of AGVHD that must be considered in deciding on a treatment strategy for individual patients.
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U2 - 10.1182/blood-2011-06-364265
DO - 10.1182/blood-2011-06-364265
M3 - Article
C2 - 22010102
AN - SCOPUS:84862908566
SN - 0006-4971
VL - 119
SP - 296
EP - 307
JO - Blood
JF - Blood
IS - 1
ER -