4.6 Article

Impact of type of reduced-intensity conditioning regimen on the outcomes of allogeneic haematopoietic cell transplantation in classical Hodgkin lymphoma

Journal

BRITISH JOURNAL OF HAEMATOLOGY
Volume 190, Issue 4, Pages 573-582

Publisher

WILEY
DOI: 10.1111/bjh.16664

Keywords

reduced-intensity conditioning; allogeneic hematopoietic cell transplant; classical Hodgkin lymphoma

Categories

Funding

  1. Public Health Service Grant from the National Cancer Institute (NCI) [5U24CA076518]
  2. National Heart, Lung and Blood Institute (NHLBI) [5U24CA076518]
  3. National Institute of Allergy and Infectious Diseases (NIAID) [5U24CA076518]
  4. NHLBI [4U10HL069294]
  5. NCI [4U10HL069294]
  6. Health Resources and Services Administration (HRSA/DHHS) [HHSH250201200016C]
  7. Office of Naval Research [N00014-17-1-2388, N00014-16-1-2020]
  8. Actinium Pharmaceuticals, Inc.
  9. Amgen, Inc.
  10. Amneal Biosciences
  11. Angiocrine Bioscience, Inc.
  12. Astellas Pharma US
  13. Atara Biotherapeutics, Inc.
  14. Be the Match Foundation
  15. bluebird bio, Inc.
  16. Bristol Myers Squibb Oncology
  17. Celgene Corporation
  18. Cerus Corporation
  19. Chimerix, Inc.
  20. Fred Hutchinson Cancer Research Center
  21. Gamida Cell Ltd.
  22. Gilead Sciences, Inc.
  23. HistoGenetics, Inc.
  24. Immucor
  25. Janssen Scientific Affairs, LLC
  26. Jazz Pharmaceuticals, Inc.
  27. Juno Therapeutics
  28. Karyopharm Therapeutics, Inc.
  29. Kite Pharma, Inc.
  30. Medac, GmbH
  31. MedImmune
  32. Medical College of Wisconsin
  33. Merck Co, Inc.
  34. Mesoblast
  35. MesoScale Diagnostics, Inc.
  36. Millennium, the Takeda Oncology Co.
  37. Miltenyi Biotec, Inc.
  38. National Marrow Donor Program
  39. Neovii Biotech NA, Inc.
  40. Novartis Pharmaceuticals Corporation
  41. Otsuka Pharmaceutical Co, Ltd. - Japan
  42. PCORI
  43. Pfizer, Inc
  44. Pharmacyclics, LLC
  45. PIRCHE AG
  46. Sanofi Genzyme
  47. Seattle Genetics
  48. Shire
  49. Spectrum Pharmaceuticals, Inc.
  50. St. Baldrick's Foundation
  51. Sunesis Pharmaceuticals, Inc.
  52. Swedish Orphan Biovitrum, Inc.
  53. Takeda Oncology
  54. Telomere Diagnostics, Inc.
  55. University of Minnesota
  56. Incyte Corporation

Ask authors/readers for more resources

Reduced-intensity conditioning (RIC) allogeneic haematopoietic cell transplantation (allo-HCT) is a curative option for select relapsed/refractory Hodgkin lymphoma (HL) patients; however, there are sparse data to support superiority of any particular conditioning regimen. We analyzed 492 adult patients undergoing human leucocyte antigen (HLA)-matched sibling or unrelated donor allo-HCT for HL between 2008 and 2016, utilizing RIC with either fludarabine/busulfan (Flu/Bu), fludarabine/melphalan (Flu/Mel140) or fludarabine/cyclophosphamide (Flu/Cy). Multivariable regression analysis was performed using a significance level of <0 center dot 01. There were no significant differences between regimens in risk for non-relapse mortality (NRM) (P = 0 center dot 54), relapse/progression (P = 0 center dot 02) or progression-free survival (PFS) (P = 0 center dot 14). Flu/Cy conditioning was associated with decreased risk of mortality in the first 11 months after allo-HCT (HR = 0 center dot 28; 95% CI = 0 center dot 10-0 center dot 73; P = 0 center dot 009), but beyond 11 months post allo-HCT it was associated with a significantly higher risk of mortality, (HR = 2 center dot 46; 95% CI = 0 center dot 1.32-4 center dot 61; P = 0 center dot 005). Four-year adjusted overall survival (OS) was similar across regimens at 62% for Flu/Bu, 59% for Flu/Mel140 and 55% for Flu/Cy (P = 0 center dot 64), respectively. These data confirm the choice of RIC for allo-HCT in HL does not influence risk of relapse, NRM or PFS. Although no OS benefit was seen between Flu/Bu and Flu/Mel 140; Flu/Cy was associated with a significantly higher risk of mortality beyond 11 months from allo-HCT (possibly due to late NRM events).

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available