4.2 Article

Impact of Pretransplant Therapy and Depth of Disease Response before Autologous Transplantation for Multiple Myeloma

Journal

BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION
Volume 21, Issue 2, Pages 335-341

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.bbmt.2014.10.023

Keywords

Myeloma; Primary refractory; Autologous transplant

Funding

  1. National Cancer Institute (NCI) [U24-CA076518]
  2. National Heart, Lung, and Blood Institute (NHLBI)
  3. National Institute of Allergy and Infectious Diseases (NIAID)
  4. NHLBI and NCI [5U10HL069294]
  5. Health Resources and Services Administration [HHSH250201200016C]
  6. Office of Naval Research [N00014-12-1-0142, N00014-13-1-0039]
  7. Office of Naval Research
  8. *Actinium Pharmaceuticals
  9. Allos Therapeutics, Inc.
  10. Amgen, Inc.
  11. Anonymous donation to the Medical College of Wisconsin
  12. Ariad
  13. Be The Match Foundation
  14. *Blue Cross and Blue Shield Association
  15. *Celgene Corporation
  16. Chimerix, Inc.
  17. Fred Hutchinson Cancer Research Center
  18. Fresenius-Biotech North America, Inc.
  19. *Gamida Cell Teva Joint Venture Ltd.
  20. Genentech, Inc.
  21. Gentium SpA
  22. Genzyme Corporation
  23. GlaxoSmithKline
  24. Health Research, Inc. Roswell Park Cancer Institute
  25. HistoGenetics, Inc.
  26. Incyte Corporation
  27. Jeff Gordon Children's Foundation
  28. Kiadis Pharma
  29. Leukemia & Lymphoma Society
  30. Medac GmbH
  31. Medical College of Wisconsin
  32. Merck Co, Inc.
  33. Millennium: The Takeda Oncology Co.
  34. Milliman USA, Inc.
  35. *Miltenyi Biotec, Inc.
  36. National Marrow Donor Program
  37. Onyx Pharmaceuticals
  38. Optum Healthcare Solutions, Inc.
  39. Osiris Therapeutics, Inc.
  40. Otsuka America Pharmaceutical, Inc.
  41. Perkin Elmer, Inc.
  42. *Remedy Informatics
  43. Sanofi US
  44. Seattle Genetics
  45. Sigma-Tau Pharmaceuticals
  46. Soligenix, Inc.
  47. St. Baldrick's Foundation
  48. StemCyte, A Global Cord Blood Therapeutics Co.
  49. Stemsoft Software, Inc.
  50. Swedish Orphan Biovitrum
  51. *Tarix Pharmaceuticals
  52. *Terumo BCT
  53. *Teva Neuroscience, Inc.
  54. *Therakos
  55. University of Minnesota
  56. University of Utah
  57. WellPoint

Ask authors/readers for more resources

Patients with multiple myeloma (MM) who are eligible for autologous stem cell transplantation (ASCT) typically receive a finite period of initial therapy before ASCT. It is not clear if patients with suboptimal (less than a partial) response to initial therapy benefit from additional alternative therapy with intent to maximize pretransplant response. We identified 539 patients with MM who had an ASCT after having achieved less than a partial response (PR) to first-line induction chemotherapy between 1995 and 2010. These patients were then divided into 2 groups: those who received additional salvage chemotherapy before ASCT (n = 324) and those who had no additional salvage chemotherapy immediately before ASCT (n = 215). Additional pretransplant chemotherapy resulted in deepening responses in 68% (complete response in 8% and PR in 60%). On multivariate analysis there was no impact of pretransplant salvage chemotherapy on treatment-related mortality, risk for relapse, progression-free survival, or overall survival. In conclusion, for patients achieving less than a PR to initial induction therapy, including with novel agent combinations, additional pre-ASCT salvage chemotherapy improved the depth of response and pre-ASCT disease status but was not associated with survival benefit. (C) 2015 American Society for Blood and Marrow Transplantation.

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