4.6 Article

Reduced intensity conditioning for acute myeloid leukemia using melphalan- vs busulfan-based regimens: a CIBMTR report

期刊

BLOOD ADVANCES
卷 4, 期 13, 页码 3180-3190

出版社

AMER SOC HEMATOLOGY
DOI: 10.1182/bloodadvances.2019001266

关键词

-

资金

  1. National Institutes of Health, National Cancer Institute (NCI)
  2. National Heart, Lung, and Blood Institute (NHLBI)
  3. National Institute of Allergy and Infectious Diseases (NIAID) [U24CA076518]
  4. NHLBI
  5. NCI [5P01CA111412, R01CA152108, 1R01CA231141, U24HL138660]
  6. Health Resources and Services Administration [HHSH250201700006C]
  7. Office of Naval Research [N0001418-1-2888, N00014-17-1-2850]
  8. HRSA subaward [SC1MC31881-01-00]
  9. NHLBI [R01HL131731, R01HL126589, 5R01HL129472, 1R01HL131731, OT3HL147741, R21HL140314, U01HL128568]
  10. National Institute of Allergy and Infectious Diseases [1U01AI126612]
  11. Actinium Pharmaceuticals Inc.
  12. Adaptive Biotechnologies
  13. Allovir Inc.
  14. Amgen Inc.
  15. Anthem Inc.
  16. HistoGenetics Inc.
  17. Astellas Pharma US
  18. Atara Biotherapeutics Inc.
  19. BARDA
  20. Be the Match Foundation
  21. bluebird bio Inc.
  22. Boston Children's Hospital
  23. Bristol Myers Squibb Co.
  24. Celgene Corp.
  25. Children's Hospital of Los Angeles
  26. Chimerix Inc.
  27. City of Hope Medical Center
  28. CSL Behring
  29. CytoSen Therapeutics Inc.
  30. Daiichi Sankyo Co. Ltd.
  31. Dana Farber Cancer Institute
  32. Enterprise Science and Computing Inc.
  33. Fred Hutchinson Cancer Research Center
  34. Gamida-Cell Ltd.
  35. Genzyme
  36. Gilead Sciences Inc.
  37. GlaxoSmithKline
  38. Immucor
  39. Incyte Corporation
  40. Janssen Biotech Inc.
  41. Janssen Pharmaceuticals Inc.
  42. Janssen Research & Development LLC
  43. Janssen Scientific Affairs LLC
  44. Japan Hematopoietic Cell Transplantation Data Center
  45. Jazz Pharmaceuticals Inc.
  46. Karius Inc.
  47. Karyopharm Therapeutics Inc.
  48. Kite (a Gilead Company)
  49. Kyowa Kirin
  50. Magenta Therapeutics
  51. Mayo Clinic
  52. Foundation Rochester
  53. Medac GmbH
  54. Mediware
  55. Memorial Sloan-Kettering Cancer Center
  56. Merck Company Inc.
  57. Mesoblast
  58. MesoScale Diagnostics Inc.
  59. Millennium
  60. Takeda Oncology Co.
  61. Miltenyi Biotec Inc.
  62. Mundipharma EDO
  63. National Marrow Donor Program
  64. Novartis Oncology
  65. Novartis Pharmaceuticals Corporation
  66. Omeros Corporation
  67. Oncoimmune Inc.
  68. OptumHealth
  69. Orca Biosystems Inc.
  70. PCORI
  71. Pfizer Inc.
  72. Phamacyclics LLC
  73. PIRCHE AG
  74. Regeneron Pharmaceuticals Inc.
  75. REGiMMUNE Corp.
  76. Sanofi Genzyme
  77. Seattle Genetics
  78. Shire
  79. Sobi Inc.
  80. Spectrum Pharmaceuticals Inc.
  81. St. Baldrick's Foundation
  82. Swedish Orphan Biovitrum Inc.
  83. Takeda Oncology
  84. Medical College of Wisconsin
  85. University of Minnesota
  86. University of Pittsburgh
  87. University of Texas-MD Anderson
  88. University of Wisconsin-Madison
  89. Viracor Eurofins
  90. Xenikos BV
  91. NATIONAL CANCER INSTITUTE [ZIACP010190] Funding Source: NIH RePORTER

向作者/读者索取更多资源

There is a lack of large comparative study on the outcomes of reduced intensity conditioning (RIC) in acute myeloid leukemia (AML) transplantation using fludarabine/busulfan (FB) and fludarabine/melphalan (FM) regimens. Adult AML patients from Center for International Blood and Marrow Transplant Research who received first RIC allo-transplant between 2001 and 2015 were studied. Patients were excluded if they received cord blood or identical twin transplant, total body irradiation in conditioning, or graft-versus-host disease (GVHD) prophylaxis with in vitro T-cell depletion. Primary outcome was overall survival (OS), secondary end points were leukemia-free survival (LFS), nonrelapse mortality (NRM), relapse, and GVHD. Multivariate survival model was used with adjustment for patient, leukemia, and transplant-related factors. A total of 622 patients received FM and 791 received FB RIC. Compared with FB, the FM group had fewer transplant in complete remission (CR), fewer matched sibling donors, and less usage of anti-thymocyte globulin or alemtuzumab. More patients in the FM group received marrow grafts and had transplantation before 2005. OS was significantly lower within the first 3 months posttransplant in the FM group (hazard ratio [HR] = 1.82, P < .001), but was marginally superior beyond 3 months (HR = 0.87, P = .05). LFS was better with FM compared with FB (HR = 0.89, P = .05). NRM was significantly increased in the FM group during the first 3 months of posttransplant (HR = 3.85, P < .001). Long-term relapse was lower with FM (HR = 0.65, P < .001). Analysis restricted to patients with CR showed comparable results. In conclusion, compared with FB, the FM RIC showed a marginally superior long-term OS and LFS and a lower relapse rate. A lower OS early posttransplant within 3 months was largely the result of a higher early NRM.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据