4.2 Article

Outcomes of Allogeneic Hematopoietic Cell Transplantation in T Cell Prolymphocytic Leukemia: A Contemporary Analysis from the Center for International Blood and Marrow Research

期刊

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jtct.2022.01.017

关键词

Prolymphocytic leukemia; T-PLL; Allogeneic stem cell transplant

资金

  1. National Cancer Institute [U24CA076518]
  2. National Heart, Lung and Blood Institute
  3. National Institute of Allergy and Infectious Diseases
  4. Health Resources and Services Administration [HHSH250201700006C]
  5. Office of Naval Research [N00014-20-1-2705, N00014-20-1-2832]
  6. Be the Match Foundation
  7. Medical College of Wisconsin
  8. National Marrow Donor Program
  9. AbbVie
  10. Accenture
  11. Actinium Pharmaceuticals
  12. Adaptive Biotechnologies
  13. Adienne SA
  14. Allovir
  15. Amgen
  16. Astellas Pharma US
  17. bluebird bio
  18. Bristol Myers Squibb
  19. CareDx
  20. CSL Behring
  21. CytoSen Therapeutics
  22. Daiichi Sankyo
  23. Eurofins Viracor
  24. ExcellThera
  25. Fate Therapeutics
  26. GamidaCell
  27. Genentech
  28. Gilead
  29. GlaxoSmithKline
  30. Incyte
  31. Janssen/Johnson Johnson
  32. Jasper Therapeutics
  33. Jazz Pharmaceuticals
  34. Karyopharm Therapeutics
  35. Kiadis Pharma
  36. Kite Pharma
  37. Kyowa Kirin
  38. Legend
  39. Magenta Therapeutics
  40. Medac
  41. Medexus
  42. Merck Co
  43. Millennium
  44. Miltenyi Biotec
  45. MorphoSys
  46. Novartis Pharmaceuticals
  47. Omeros
  48. Oncopeptides
  49. Orca Biosystems
  50. Ossium Health
  51. Pfizer
  52. Pharmacyclics
  53. Priothera
  54. Sanofi Genzyme
  55. Seagen
  56. Stemcyte
  57. Takeda Pharmaceuticals
  58. Tscan
  59. Vertex
  60. Vor Biopharma
  61. Xenikos BV

向作者/读者索取更多资源

This study analyzed the outcomes of alloHCT in 266 patients with T-PLL and aimed to identify predictors of post-transplantation relapse and survival. The results showed that reduced-intensity conditioning alloHCT was associated with long-term disease-free survival.
T cell prolymphocytic leukemia (T-PLL) is a rare, aggressive malignancy with limited treatment options and poor long-term survival. Previous studies of allogeneic hematopoietic cell transplantation (alloHCT) for T-PLL are limited by small numbers, and descriptions of patient and transplantation characteristics and outcomes after alloHCT are sparse. In this study, we evaluated outcomes of alloHCT in patients with T-PLL and attempted to identify predictors of post-transplantation relapse and survival. We conducted an analysis of data using the Center for International Blood and Marrow Transplant Research database on 266 patients with T-PLL who underwent alloHCT between 2008 and 2018. The 4-year rates of overall survival (OS), disease-free survival (DFS), relapse, and treatment-related mortality (TRM) were 30.0% (95% confidence interval [CI], 23.8% to 36.5%), 25.7% (95% CI, 20% to 32%), 41.9% (95% CI, 35.5% to 48.4%), and 32.4% (95% CI, 26.4% to 38.6%), respectively. In multivariable analyses, 3 variables were associated with inferior OS: receipt of a myeloablative conditioning (MAC) regimen (hazard ratio [HR], 2.18; P <.0001), age >60 years (HR, 1.61; P =.0053), and suboptimal performance status, defined by Karnofsky Performance Status (KPS) <90 (HR, 1.53; P =.0073). Receipt of an MAC regimen also was associated with increased TRM (HR, 3.31; P <.0001), an elevated cumulative incidence of grade II-IV acute graft-versus-host disease (HR, 2.94; P =.0011), and inferior DFS (HR, 1.86; P =.0004). Conditioning intensity was not associated with relapse; however, stable disease/progression was correlated with increased risk of relapse (HR, 2.13; P =.0072). Both in vivo T cell depletion (TCD) as part of conditioning and KPS <90 were associated with worse TRM and inferior DFS. Receipt of total body irradiation had no significant effect on OS, DFS, or TRM. Our data show that reduced-intensity conditioning without in vivo TCD (ie, without antithymocyte globulin or alemtuzumab) before alloHCT was associated with long-term DFS in patients with T-PLL who were age <= 60 years or who had a KPS >90 or chemosensitive disease. (c) 2022 The American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. All rights reserved.

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