4.7 Article

Reduced intensity conditioning is superior to nonmyeloablative conditioning for older chronic myelogenous leukemia patients undergoing hematopoietic cell transplant during the tyrosine kinase inhibitor era

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BLOOD
卷 119, 期 17, 页码 4083-4090

出版社

AMER SOC HEMATOLOGY
DOI: 10.1182/blood-2012-02-409763

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资金

  1. US Public Health Service from National Cancer Institute (NCI) [U24-CA76518, 5U01HL069294]
  2. National Heart, Lung, and Blood Institute (NHLBI) [5U01HL069294]
  3. National Institute of Allergy and Infectious Diseases
  4. Health Resources and Services Administration [HHSH234200637015C]
  5. Office of Naval Research [N00014-06-1-0704, N00014-08-1-0058]
  6. AABB (National Blood Foundation)
  7. Allos Inc
  8. Amgen Inc
  9. Astellas Pharma US Inc
  10. Be the Match Foundation
  11. Biogen IDEC
  12. Bio-Marin Pharmaceutical Inc
  13. Biovitrum AB
  14. BloodCenter of Wisconsin
  15. Blue Cross and Blue Shield Association
  16. Bone Marrow Foundation
  17. Buchanan Family Foundation
  18. CaridianBCT
  19. Celgene Corporation
  20. CellGenix GmbH
  21. Children's Leukemia Research Association
  22. ClinImmune Labs
  23. CTI Clinical Trial and Consulting Services
  24. Eisai Inc
  25. Genentech Inc
  26. Genzyme Corporation
  27. Histogenetics Inc
  28. HKS Medical Information Systems
  29. Hospira Inc
  30. Kirin Brewery Co Ltd
  31. The Leukemia & Lymphoma Society
  32. Merck Company
  33. Medical College of Wisconsin
  34. Millennium Pharmaceuticals Inc
  35. Miller Pharmacal Group
  36. Milliman USA Inc
  37. Miltenyi Biotec Inc
  38. National Marrow Donor Program
  39. Nature Publishing Group
  40. Novartis Oncology
  41. Oncology Nursing Society
  42. Osiris Therapeutics Inc
  43. Otsuka America Pharmaceutical Inc
  44. Pall Life Sciences
  45. Pfizer Inc
  46. Schering Corporation
  47. Sigma-Tau Pharmaceuticals
  48. Soligenix Inc
  49. StemCyte Inc
  50. StemSoft Software Inc
  51. Sysmex America Inc
  52. THERAKOS Inc
  53. Vidacare Corporation
  54. ViraCor Laboratories
  55. ViroPharma Inc
  56. Wellpoint Inc

向作者/读者索取更多资源

Tyrosine kinase inhibitors (TKIs) and reduced intensity conditioning (RIC)/nonmyeloablative (NMA) conditioning hematopoietic cell transplants (HCTs) have changed the therapeutic strategy for chronic myelogenous leukemia (CML) patients. We analyzed post-HCT outcomes of 306 CML patients reported to the Center for International Blood and Marrow Transplant Research aged 40 years and older undergoing RIC/NMA HCT from 2001 to 2007: 117 (38%) aged 40 to 49 years, 119 (39%) 50 to 59 years, and 70 (23%) 60 years or older. The majority (74%) had treatment with imatinib before HCT. At HCT, most patients aged 40 to 49 years were in chronic phase (CP) 1 (74%), compared with 31% aged 60 years or older. Siblings were donors for 56% aged 40 to 49 years; older cohorts had more unrelated donors. The majority received peripheral blood grafts and RIC across all age groups. 3 year overall survival (54%, 52%, and 41%), day + 100 grade II-IV acute GVHD (26%, 32%, and 32%), chronic GVHD (58%, 51%, and 43%), and 1-year treatment-related mortality (18%, 20%, and 13%) were similar across ages. The 3-year relapse incidence (36%, 43%, and 66%) and disease-free survival (35%, 32%, and 16%) were inferior in the oldest cohort. Importantly, for CP1 patients, relapse and disease-free survival were similar across age cohorts. Allogeneic RIC HCT for older patients with CML can control relapse with acceptable toxicity and survival in TKI-exposed CML, especially if still in CP1. (Blood. 2012;119(17):4083-4090)

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