4.6 Article

HLA-matching with PTCy: a reanalysis of a CIBMTR dataset with propensity score matching and donor age

期刊

BLOOD ADVANCES
卷 6, 期 14, 页码 4335-4346

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ELSEVIER
DOI: 10.1182/bloodadvances.2022007741

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资金

  1. National Institutes of Health (NIH) National Cancer Institute (NCI) [P01 CA225618, P30 CA006973]
  2. Public Health Service from National Cancer Institute (NCI) [U24CA076518]
  3. National Heart, Lung, and Blood Institute (NHLBI)
  4. National Institute of Allergy and Infectious Diseases (NIAID)
  5. Health Resources and Services Administration (HRSA) [HHSH250201700006C]
  6. Office of Naval Research [N00014-20-1-2832, N00014-21-1-2954]
  7. Be the Match Foundation
  8. Medical College of Wisconsin
  9. National Marrow Donor Program
  10. AbbVie
  11. Actinium Pharmaceuticals, Inc.
  12. Adaptive Biotechnologies Corporation
  13. Adienne SA
  14. Allogene
  15. Allovir, Inc.
  16. Amgen, Inc.
  17. Anthem
  18. Astellas Pharma US
  19. Atara Biotherapeutics
  20. bluebird bio, inc.
  21. Bristol Myers Squibb Co.
  22. CareDx Inc.
  23. CRISPR
  24. CSL Behring
  25. CytoSen Therapeutics, Inc.
  26. Daiichi Sankyo Co., Ltd.
  27. Eurofins Viracor
  28. DBA Eurofins Transplant Diagnostics
  29. Fate Therapeutics
  30. Gamida-Cell, Ltd.
  31. Gilead
  32. GlaxoSmithKline
  33. HistoGenetics
  34. Incyte Corporation
  35. Iovance
  36. Janssen Research & Development, LLC
  37. Janssen/Johnson Johnson
  38. Jasper Therapeutics
  39. Jazz Pharmaceuticals, Inc.
  40. Kadmon
  41. Karius
  42. Kiadis Pharma
  43. Kite, a Gilead Company
  44. Kyowa Kirin
  45. Legend Biotech
  46. Magenta Therapeutics
  47. Mallinckrodt Pharmaceuticals
  48. Medac GmbH
  49. Medexus
  50. Merck Co.
  51. Millennium
  52. Takeda Oncology Co.
  53. Miltenyi Biotec, Inc.
  54. MorphoSys
  55. Novartis Pharmaceuticals Corporation
  56. Omeros Corporation
  57. OptumHealth
  58. Orca Biosystems, Inc.
  59. Ossium Health, Inc
  60. Pfizer, Inc.
  61. Pharmacyclics, LLC
  62. Priothera
  63. Sanofi Genzyme
  64. Stemcyte
  65. Takeda Pharmaceuticals
  66. Talaris Therapeutics
  67. Terumo Blood and Cell Technologies
  68. TG Therapeutics
  69. Tscan
  70. Vertex
  71. Xenikos BV

向作者/读者索取更多资源

This study compares the outcomes of blood or marrow transplantation using haploidentical donors and HLA-matched donors with different prophylactic methods. The results suggest that there is no significant difference in overall survival, disease-free survival, relapse rate, and nonrelapse mortality between the two groups. The impact of HLA matching on transplant outcomes with posttransplant cyclophosphamide may be less meaningful than previously reported.
Blood or marrow transplantation (BMT) outcomes using haploidentical donors (Haplo) and posttransplant cyclophosphamide (PTCy)-based graft-versus-host disease (GVHD) prophylaxis compare favorably to HLA-matched donors using calcineurin inhibitor-based prophylaxis. A recent Center for International Blood and Marrow Transplant Research analysis of patients receiving homogenous PTCy-based prophylaxis found that, with reduced intensity conditioning, Haplo BMTs had worse outcomes than matched unrelated donor (MUD) BMTs. Due to significant differences between groups, we reanalyzed the dataset using propensity score matching and, additionally, added a donor age variable. After matching MUD BMTs to Haplo BMTs in a 1:5 ratio, no significant differences were found between groups across all measured baseline characteristics. Outcomes analyses demonstrated no significant differences in overall survival (hazard ratio [HR] of mortality with MUD vs Haplo [95% confidence interval], 0.95 [0.65-1.16], P = .75), disease-free survival (HR of relapse or death, 0.98 [0.73-1.18], P = .89), relapse rate (HR, 1.06 [0.77-1.38], P = .69), or nonrelapse mortality (NRM) (HR, 0.85 [0.42-1.13], P = .49) between groups. After stratification by conditioning intensity, MUD BMTs in the reduced-intensity cohort had lower risk of NRM (HR, 0.56 [0.14-0.99], P = .05), with no significant difference in other clinical outcomes. These results suggest the effect of HLA matching on BMT outcomes with PTCy is less meaningful than previously reported. Timely identification of a young, at least half-matched (related or unrelated) donor may be more important than finding a fully matched donor if the latter leads to a delay in BMT or use of an older donor.

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