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Risk factors for acute GVHD and survival after hematopoietic cell transplantation

  • Madan Jagasia
  • , Mukta Arora
  • , Mary E D Flowers
  • , Nelson J. Chao
  • , Philip L. McCarthy
  • , Corey S. Cutler
  • , Alvaro Urbano-Ispizua
  • , Steven Z. Pavletic
  • , Michael D. Haagenson
  • , Mei Jie Zhang
  • , Joseph H. Antin
  • , Brian J. Bolwell
  • , Christopher Bredeson
  • , Jean Yves Cahn
  • , Mitchell Cairo
  • , Robert Peter Gale
  • , Vikas Gupta
  • , Stephanie J. Lee
  • , Mark Litzow
  • , Daniel J. Weisdorf
  • Mary M. Horowitz, Theresa Hahn

Research output: Contribution to journalArticlepeer-review

Abstract

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.

Original languageEnglish (US)
Pages (from-to)296-307
Number of pages12
JournalBlood
Volume119
Issue number1
DOIs
StatePublished - Jan 5 2012

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