4.7 Article

Risk factors for acute GVHD and survival after hematopoietic cell transplantation

期刊

BLOOD
卷 119, 期 1, 页码 296-307

出版社

AMER SOC HEMATOLOGY
DOI: 10.1182/blood-2011-06-364265

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资金

  1. National Cancer Institute (NCI) [U24-CA76518]
  2. National Heart, Lung, and Blood Institute (NHLBI)
  3. National Institute of Allergy and Infectious Diseases (NIAID)
  4. NHLBI [5U01HL069294]
  5. NCI
  6. Health Resources and Services Administration [HHSH234200637015C]
  7. Office of Naval Research [N00014-061-0704, N00014-08-1-0058]
  8. Allos Inc
  9. Amgen Inc
  10. Angioblast
  11. Ariad
  12. Be the Match Foundation
  13. Blue Cross and Blue Shield Association
  14. Buchanan Family Foundation
  15. CaridianBCT
  16. Celgene Corporation
  17. CellGenix, GmbH
  18. Children's Leukemia Research Association
  19. Fresenius-Biotech North America Inc
  20. Gamida Cell Teva Joint Venture Ltd
  21. Genentech Inc
  22. Genzyme Corporation
  23. GlaxoSmithKline
  24. Kiadis Pharma
  25. Leukemia & Lymphoma Society
  26. Medical College of Wisconsin
  27. Millennium Pharmaceuticals Inc
  28. Milliman USA Inc
  29. Miltenyi Biotec Inc
  30. National Marrow Donor Program
  31. Optum Healthcare Solutions Inc
  32. Otsuka America Pharmaceutical Inc
  33. Seattle Genetics
  34. Sigma-Tau Pharmaceuticals
  35. Soligenix Inc
  36. Swedish Orphan Biovitrum
  37. THERAKOS Inc
  38. Wellpoint Inc

向作者/读者索取更多资源

Risk factors for acute GVHD (AGVHD), overall survival, and transplant-related mortality were evaluated in adults receiving allogeneic hematopoietic cell transplants (19992005) 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 on AGVHD risk, 6 treatment categories were evaluated: (1) myeloablative conditioning (MA) with total body irradiation (TBI) + PBSCs, (2) MA + TBI + BM, (3) MA + nonTBI + PBSCs, (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, orRIC + PBSCs had lower risks of grades B-D AGVHD 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. (Blood. 2012; 119(1): 296-307)

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