4.7 Article

Better leukemia-free and overall survival in AML in first remission following cyclophosphamide in combination with busulfan compared with TBI

期刊

BLOOD
卷 122, 期 24, 页码 3863-3870

出版社

AMER SOC HEMATOLOGY
DOI: 10.1182/blood-2013-07-514448

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资金

  1. National Cancer Institute [U24- CA76518, HHSH234200637015C]
  2. National Heart, Lung and Blood Institute
  3. National Institute of Allergy and Infectious Diseases
  4. National Heart, Lung and Blood Institute [5U01HL069294]
  5. Health Resources and Services Administration (HRSA/DHHS)
  6. Office of Naval Research [N00014-06-1-0704, N00014-08-1-0058]
  7. Allos, Inc.
  8. Amgen, Inc.
  9. Angioblast
  10. Ariad
  11. Be the Match Foundation
  12. Blue Cross
  13. Blue Shield Association
  14. Buchanan Family Foundation
  15. CaridianBCT
  16. Celgene Corporation
  17. CellGenix
  18. GmbH
  19. Children's Leukemia Research Association
  20. Fresenius-Biotech North America, Inc.
  21. Gamida Cell Teva Joint Venture Ltd.
  22. Genentech, Inc.
  23. Genzyme Corporation
  24. GlaxoSmithKline
  25. Kiadis Pharma
  26. Leukemia & Lymphoma Society
  27. Medical College of Wisconsin
  28. Millennium Pharmaceuticals, Inc.
  29. Milliman USA, Inc.
  30. Miltenyi Biotec, Inc.
  31. National Marrow Donor Program
  32. Optum Healthcare Solutions, Inc.
  33. Otsuka America Pharmaceutical, Inc.
  34. Seattle Genetics
  35. Sigma-tau Pharmaceuticals
  36. Soligenix, Inc.
  37. Swedish Orphan Biovitrum
  38. THERAKOS, Inc.
  39. Wellpoint, Inc.

向作者/读者索取更多资源

Cyclophosphamide combined with total body irradiation (Cy/TBI) or busulfan (BuCy) are the most widely used myeloablative conditioning regimens for allotransplants. Recent data regarding their comparative effectiveness are lacking. We analyzed data from the Center for International Blood and Marrow Transplant Research for 1230 subjects receiving a first hematopoietic cell transplant from a human leukocyte antigen-matched sibling or from an unrelated donor during the years 2000 to 2006 for acute myeloid leukemia (AML) in first complete remission (CR) after conditioning with Cy/TBI or oral or intravenous (IV) BuCy. Multivariate analysis showed significantly less nonrelapse mortality (relative risk [RR] = 0.58; 95% confidence interval [CI]: 0.39-0.86; P = .007), and relapse after, but not before, 1 year posttransplant (RR = 0.23; 95% CI: 0.08-0.65; P = .006), and better leukemia-free survival (RR = 0.70; 95% CI: 0.55-0.88; P = .003) and survival (RR = 0.68; 95% CI: 0.52-0.88; P = .003) in persons receiving IV, but not oral, Bu compared with TBI. In combination with Cy, IV Bu is associated with superior outcomes compared with TBI in patients with AML in first CR. (Blood. 2013;122(24):3863-3870)

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