4.5 Article

Impact of depth of clinical response on outcomes of acute myeloid leukemia patients in first complete remission who undergo allogeneic hematopoietic cell transplantation

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BONE MARROW TRANSPLANTATION
卷 56, 期 9, 页码 2108-2117

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SPRINGERNATURE
DOI: 10.1038/s41409-021-01261-6

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资金

  1. Public Health Service from the National Cancer Institute (NCI) [U24CA076518]
  2. Public Health Service from the National Heart, Lung and Blood Institute (NHLBI) [U24CA076518]
  3. Public Health Service from the National Institute of Allergy and Infectious Diseases (NIAID) [U24CA076518]
  4. NHLBI [U24HL138660, OT3HL147741, U01HL128568]
  5. NCI [U24HL138660]
  6. Health Resources and Services Administration (HRSA) [HHSH250201700006C, HHSH250201700007C]
  7. Office of Naval Research [N00014-20-1-2705, N00014-20-12832]
  8. BARDA
  9. Be the Match Foundation
  10. Boston Children's Hospital
  11. Dana Farber
  12. St. Baldrick's Foundation
  13. Stanford University
  14. Medical College of Wisconsin the National Marrow Donor Program
  15. Actinium Pharmaceuticals, Inc.
  16. Adienne SA
  17. Allovir, Inc.
  18. Amgen, Inc.
  19. Angiocrine Bioscience
  20. Astellas Pharma US
  21. bluebird bio, Inc.
  22. Bristol Myers Squibb Co.
  23. Celgene Corp.
  24. CSL Behring
  25. CytoSen Therapeutics, Inc.
  26. Daiichi Sankyo Co., Ltd.
  27. ExcellThera
  28. Fate Therapeutics
  29. Gamida-Cell, Ltd.
  30. Genentech Inc
  31. Incyte Corporation
  32. Janssen/Johnson Johnson
  33. Jazz Pharmaceuticals, Inc.
  34. Kiadis Pharma
  35. Kite, a Gilead Company
  36. Kyowa Kirin
  37. Legend Biotech
  38. Magenta Therapeutics
  39. Merck Sharp Dohme Corp.
  40. Millennium, the Takeda Oncology Co.
  41. Miltenyi Biotec, Inc.
  42. Novartis Pharmaceuticals Corporation
  43. Omeros Corporation
  44. Oncoimmune, Inc.
  45. Orca Biosystems, Inc.
  46. Pfizer, Inc.
  47. Pharmacyclics, LLC
  48. Sanofi Genzyme
  49. Stemcyte
  50. Takeda Pharma
  51. Vor Biopharma
  52. Xenikos BV
  53. [P01CA111412]
  54. [R01CA152108]
  55. [R01CA215134]
  56. [R01CA218285]
  57. [R01CA231141]
  58. [R01AI128775]
  59. [R01HL126589]
  60. [R01HL129472]
  61. [R01HL130388]
  62. [R01HL131731]
  63. [U01AI069197]
  64. [U01AI126612]
  65. [UG1HL06924]

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The study found that in AML patients, those in CRi had increased risk of death compared to those in CR, along with higher non-relapse mortality, shorter disease-free survival, and increased relapse. Detectable MRD was associated with shorter overall survival, shorter disease-free survival, higher non-relapse mortality, and increased relapse. The detrimental effects of CRi and MRD were independent.
Acute myeloid leukemia (AML) patients often undergo allogeneic hematopoietic cell transplantation (alloHCT) in first complete remission (CR). We examined the effect of depth of clinical response, including incomplete count recovery (CRi) and/or measurable residual disease (MRD), in patients from the Center for International Blood and Marrow Transplantation Research (CIBMTR) registry. We identified 2492 adult patients (1799 CR and 693 CRi) who underwent alloHCT between January 1, 2007 and December 31, 2015. The primary outcome was overall survival (OS). Multivariable analysis was performed to adjust for patient-, disease-, and transplant-related factors. Baseline characteristics were similar. Patients in CRi compared to those in CR had an increased likelihood of death (HR: 1.27; 95% confidence interval: 1.13-1.43). Compared to CR, CRi was significantly associated with increased non-relapse mortality (NRM), shorter disease-free survival (DFS), and a trend toward increased relapse. Detectable MRD was associated with shorter OS, shorter DFS, higher NRM, and increased relapse compared to absence of MRD. The deleterious effects of CRi and MRD were independent. In this large CIBMTR cohort, survival outcomes differ among AML patients based on depth of CR and presence of MRD at the time of alloHCT. Further studies should focus on optimizing post-alloHCT outcomes for patients with responses less than CR.

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