4.7 Article

Donor, recipient, and transplant characteristics as risk factors after unrelated donor PBSC transplantation: beneficial effects of higher CD34+ cell dose

期刊

BLOOD
卷 114, 期 13, 页码 2606-2616

出版社

AMER SOC HEMATOLOGY
DOI: 10.1182/blood-2009-03-208355

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资金

  1. National Marrow Donor Program and the Health Resources and Services Administration [240-97-0036, 231-02-0007]
  2. National Cancer Institute [U24-CA76518]
  3. National Institute of Allergy and Infectious Diseases
  4. National Heart, Lung and Blood Institute
  5. Office of Naval Research
  6. Health Services Research Administration (DHHS)
  7. Abbott Laboratories
  8. Aetna
  9. American International Group Inc
  10. American Red Cross
  11. Amgen Inc
  12. AnorMED Inc
  13. Astellas Pharma US Inc
  14. Baxter International Inc
  15. Berlex Laboratories Inc
  16. Biogen IDEC Inc
  17. BloodCenter of Wisconsin
  18. Blue Cross and Blue Shield Association
  19. Bristol-Myers Squibb Company
  20. BRT Laboratories Inc
  21. Cangene Corporation
  22. Celgene Corporation
  23. CellGenix Inc
  24. Cell Therapeutics Inc
  25. CelMed Biosciences
  26. Cylex Inc
  27. Cytonome Inc
  28. CytoTherm
  29. DOR BioPharma Inc
  30. Dynal Biotech, an Invitrogen Company
  31. Enzon Pharmaceuticals Inc
  32. Gambro BCT Inc
  33. Gamida Cell Ltd
  34. Genzyme Corporation
  35. Gift of Life Bone Marrow Foundation
  36. GlaxoSmithKline Inc
  37. Histogenetics Inc
  38. HKS Medical Information Systems
  39. Kirin Brewery Co Ltd
  40. Merck Company
  41. The Medical College of Wisconsin
  42. Millennium Pharmaceuticals Inc
  43. Miller Pharmacal Group
  44. Milliman USA Inc
  45. Miltenyi Biotec Inc
  46. MultiPlan Inc
  47. National Marrow Donor Program
  48. Nature Publishing Group
  49. Novartis Pharmaceuticals Inc
  50. Osiris Therapeutics Inc
  51. Pall Medical
  52. Pfizer Inc
  53. Pharmion Corporation
  54. PDL BioPharma, Inc
  55. Roche Laboratories
  56. Sanofi-aventis
  57. Schering Plough Corporation
  58. StemCyte Inc
  59. StemSoft Software Inc
  60. SuperGen, Inc
  61. Sysmex
  62. The Marrow Foundation
  63. THERAKOS Inc
  64. University of Colorado Cord Blood Bank
  65. ViaCell Inc
  66. University of Colorado Cord Blood Bank
  67. ViaCell Inc
  68. ViraCor Laboratories
  69. Wellpoint Inc
  70. Zelos Therapeutics Inc
  71. Bundesministerium fur Bildung und Forschung (Kompetenznetz Akute und chronische Leukamien Germany [01GI9981]

向作者/读者索取更多资源

We report outcomes of 932 recipients of unrelated donor peripheral blood stem cell hematopoietic cell transplantation (URD-PBSC HCT) for acute myeloid leukemia, acute lymphoblastic leukemia, chronic myelogenous leukemia, and myelodysplastic syndrome enrolled on a prospective National Marrow Donor Program trial from 1999 through 2003. Preparative regimens included myeloablative (MA; N = 611), reduced-intensity (RI; N = 160), and nonmyeloablative (NMA; N = 161). For MA recipients, CD34(+) counts greater than 3.8 X 10(6)/kg improved neutrophil and platelet engraftment, whereas improved overall survival (OS) and reduced transplant-related mortality (TRM) were seen for all preparative regimens when CD34(+) cell doses exceeded 4.5 X 10(6)/kg. Higher infused doses of CD34(+) cell dose did not result in increased rates of either acute or chronic graft-versus-host disease (GVHD). Three-year OS and disease-free survival (DFS) of recipients of MA, RI, and NMA approaches were similar (33%, 35%, and 32% OS; 33%, 30%, and 29% DFS, respectively). In summary, recipients of URD-PBSC HCT receiving preparative regimens differing in intensity experienced similar survival. Higher CD34(+) cell doses resulted in more rapid engraftment, less TRM, and better 3-year OS (39% versus 25%, MA, P = .004; 38% versus 21% RI/NMA, P = .004) but did not increase the risk of GVHD. This trial was registered at www.clinicaltrials.gov as #NCT00785525. (Blood. 2009; 114: 2606-2616)

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