4.2 Article

Autologous/Allogeneic Hematopoietic Cell Transplantation versus Tandem Autologous Transplantation for Multiple Myeloma: Comparison of Long-Term Postrelapse Survival

Journal

BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION
Volume 24, Issue 3, Pages 478-485

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.bbmt.2017.10.024

Keywords

Allogeneic transplantation; Myeloma; Relapse; Survival

Funding

  1. National Cancer Institute (NCI) [U24-CA076518]
  2. National Heart, Lung, and Blood Institute (NHLBI) [U24-CA076518]
  3. National Institute of Allergy and Infectious Diseases [U24-CA076518]
  4. NHLBI [5U10HL069294]
  5. NCI [5U10HL069294]
  6. Health Resources and Services Administration [HHSH250201200016C]
  7. Office of Naval Research [N00014-13-1-0039, N00014-14-1-0028]
  8. Actinium Pharmaceuticals
  9. Allos Therapeutics, Inc.
  10. Amgen, Inc.
  11. Ariad
  12. Be the Match Foundation
  13. Blue Cross and Blue Shield Association
  14. Celgene Corporation
  15. Chimerix, Inc.
  16. Fred Hutchinson Cancer Research Center
  17. Fresenius-Biotech North America, Inc.
  18. Gamida Cell Teva Joint Venture Ltd.
  19. Genentech, Inc.
  20. Gentium SpA
  21. Genzyme Corporation
  22. GlaxoSmithKline
  23. Health Research, Inc. Roswell Park Cancer Institute
  24. HistoGenetics, Inc.
  25. Incyte Corporation
  26. Jeff Gordon Children's Foundation
  27. Kiadis Pharma
  28. Leukemia & Lymphoma Society
  29. Medac GmbH
  30. Medical College of Wisconsin
  31. Merck Co, Inc.
  32. Millennium: The Takeda Oncology Co.
  33. Milliman USA, Inc.
  34. Miltenyi Biotec, Inc.
  35. National Marrow Donor Program
  36. Onyx Pharmaceuticals
  37. Optum Healthcare Solutions, Inc.
  38. Osiris Therapeutics, Inc.
  39. Otsuka America Pharmaceutical, Inc.
  40. Perkin Elmer, Inc.
  41. Remedy Informatics
  42. Sanofi US
  43. Seattle Genetics
  44. Sigma-Tau Pharmaceuticals
  45. Soligenix, Inc.
  46. St. Baldrick's Foundation
  47. StemCyte, A Global Cord Blood Therapeutics Co.
  48. Stemsoft Software, Inc.
  49. Swedish Orphan Biovitrum
  50. Tarix Pharmaceuticals
  51. TerumoBCT
  52. Teva Neuroscience, Inc.
  53. THERAKOS, Inc.
  54. University of Minnesota
  55. University of Utah
  56. Wellpoint, Inc.
  57. NATIONAL CANCER INSTITUTE [U24CA076518] Funding Source: NIH RePORTER
  58. NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [U10HL069294] Funding Source: NIH RePORTER

Ask authors/readers for more resources

We compared postrelapse overall survival (OS) after autologous/allogeneic (auto/alto) versus tandem autologous (auto/auto) hematopoietic cell transplantation (HCT) in patients with multiple myeloma (MM). Postrelapse survival of patients receiving an auto/auto or auto/alto HCT for MM and prospectively reported to the Center for International Blood and Marrow Transplant Research between 2000 and 2010 were analyzed. Relapse occurred in 404 patients (72.4%) in the auto/auto group and in 178 patients (67.4%) in the auto/alto group after a median follow-up of 8.5 years. Relapse occurred before 6 months after a second HCT in 46% of the auto/ allo patients, compared with 26% of the auto/auto patients. The 6-year postrelapse survival was better in the auto/alto group compared with the auto/auto group (44% versus 35%; P=.05). Mortality due to MM was 69% (n=101) in the auto/allo group and 83% (n=229) deaths in auto/auto group. In multivariate analysis, both cohorts had a similar risk of death in the first year after relapse (hazard ratio [FIR],.72; P=.12); however, for time points beyond 12 months after relapse, overall survival was superior in the auto/allo cohort (HR for death in auto/auto=1.55; P=.005). Other factors associated with superior survival were enrollment in a clinical trial for HCT, male sex, and use of novel agents at induction before HCT. Our findings shown superior survival after relapse in auto/allo HCT recipients compared with auto/auto HCT recipients. This likely reflects a better response to salvage therapy, such as immunomodulatory drugs, potentiated by a donor-derived immunologic milieu. Further augmentation of the post-allo-HCT immune system with new immunotherapies, such as monoclonal antibodies, checkpoint inhibitors, and others, merit investigation. (C) 2017 American Society for Blood and Marrow Transplantation.

Authors

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

Reviews

Primary Rating

4.2
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available