4.6 Article

Outcome of allogeneic transplantation for mature T-cell lymphomas: impact of donor source and disease characteristics

Journal

BLOOD ADVANCES
Volume 6, Issue 3, Pages 920-930

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ELSEVIER

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Funding

  1. CIBMTR
  2. EBMT
  3. Public Health Service grant from the National Cancer Institute [U24CA076518]
  4. National Heart, Lung, and Blood Institute
  5. National Institute of Allergy and Infectious Diseases
  6. Health Resources and Services Administration [HHSH250201700006C]
  7. Office of Naval Research [N00014-20-1-2705, N00014-20-1-2832]
  8. Be the Match Founda-tion
  9. Medical College of Wisconsin
  10. National Marrow Donor Program
  11. Actinium Phar-maceuticals
  12. ADIENNE
  13. AlloVir
  14. Amgen
  15. Angiocrine Bioscience
  16. Astellas Pharma US
  17. bluebird bio
  18. Bristol Myers Squibb
  19. Celgene
  20. CSL Behring
  21. CytoSen Therapeutics
  22. Daiichi Sankyo Company
  23. ExCellThera
  24. Fate Therapeutics
  25. Gamida Cell
  26. Genentech
  27. Incyte Corporation
  28. Janssen/Johnson Johnson
  29. Jazz Pharmaceuticals
  30. Kia-dis Pharma
  31. Kite
  32. Gilead Company
  33. Kyowa Kirin
  34. Legend Biotech
  35. Magenta Therapeutics
  36. Merck Sharp Dohme
  37. Millennium
  38. Takeda Oncology
  39. Miltenyi Biotec
  40. Novartis Pharmaceuticals
  41. Omeros
  42. OncoImmune
  43. Orca Biosystems
  44. Pfizer
  45. Pharmacyclics
  46. Sanofi Gen-zyme
  47. StemCyte
  48. Takeda Pharma
  49. Vor Biopharma
  50. Xenikos BV

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This study evaluated the outcomes of different types of allo-HCT in mature T-cell lymphomas and found no significant differences in survival and progression between the different groups. Results suggest that haplo-HCT can be comparable to matched sibling donor HCT.
Mature T-cell lymphomas constitute the most common indication for allogeneic hematopoietic cell transplantation (allo-HCT) of all lymphomas. Large studies evaluating contemporary outcomes of allo-HCT in mature T-cell lymphomas relative to commonly used donor sources are not available. Included in this registry study were adult patients who had undergone allo-HCT for anaplastic large cell lymphoma, angioimmunoblastic T-cell lymphoma (AITL), or peripheral T-cell lymphoma not otherwise specified (PTCL-NOS) between 2008 and 2018. Hematopoietic cell transplantation (HCT) platforms compared were posttransplant cyclophosphamidebased haploidentical (haplo-)HCT, matched sibling donor (MSD) HCT, matched unrelated donor HCT with in vivo T-cell depletion (MUD TCD+), and matched unrelated donor HCT without in vivo T-cell depletion (MUD TCD-). Coprimary end points were overall survival (OS) and progression-free survival (PFS); secondary end points included nonrelapse mortality (NRM), and relapse/progression incidence (RI). A total of 1942 patients were eligible (237 haplo-HCT; 911 MSD; 468 MUD TCD+; 326 MUD TCD-). Cohorts were comparable for baseline characteristics with the exception of higher proportions of patients with decreased performance status (PS) and marrow graft recipients in the haplo-HCT group. Using univariate and multivariate comparisons, OS, PFS, RI, and NRM were not significantly different among the haplo-HCT, MSD, MUD TCD+, and MUD TCD- cohorts, with 3-year OS and PFS of 60%, 63%, 59%, and 64%, respectively, and 50%, 50%, 48%, and 52%, respectively. Significant predictors of inferior OS and PFS on multivariate analysis were active disease status at HCT and decreased PS. AITL was associated with significantly reduced relapse risk and better PFS compared with PTCL-NOS. Allo-HCT can provide durable PFS in patients with mature T-cell lymphoma (TCL). Outcomes of haplo-HCT were comparable to those of matched donor allo-HCT.

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