4.2 Article

Autologous Transplantation in Follicular Lymphoma with Early Therapy Failure: A National LymphoCare Study and Center for International Blood and Marrow Transplant Research Analysis

Journal

BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION
Volume 24, Issue 6, Pages 1163-1171

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.bbmt.2017.12.771

Keywords

Follicular lymphoma; Early therapy failure; Autologous transplantation; Early transplant; Rituximab; Chemoimmunotherapy

Funding

  1. Public Health Service from the National Cancer Institute [U24-CA076518]
  2. Public Health Service from the National Heart, Lung, and Blood Institute [U24-CA076518]
  3. Public Health Service from the National Institute of Allergy and Infectious Diseases [U24-CA076518]
  4. National Heart, Lung, and Blood Institute [5U10HL069294]
  5. National Cancer Institute [5U10HL069294]
  6. Health Resources and Services Administration [HHSH250201200016C]
  7. Actinium Pharmaceuticals
  8. Karyopharm Therapeutics
  9. Amgen, Inc.
  10. Ariad
  11. Be The Match Foundation
  12. Blue Cross
  13. Celgene Corporation
  14. Chimerix, Inc.
  15. Fred Hutchinson Cancer Research Center
  16. Fresenius-Biotech North America, Inc.
  17. Gamida Cell Teva Joint Venture Ltd.
  18. Genentech, Inc.
  19. Gentium SpA
  20. Genzyme Corporation
  21. GlaxoSmithKline
  22. Health Research, Inc.
  23. 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
  35. National Marrow Donor Program
  36. Onyx Pharmaceuticals
  37. Optum Healthcare Solutions, Inc.
  38. Osiris Therapeutics
  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. Blue Shield Association
  58. Office of Naval Research [N00014-13-1-0039, N00014-14-1-0028]
  59. NATIONAL CANCER INSTITUTE [U24CA076518, P50CA097274, P30CA086862] Funding Source: NIH RePORTER
  60. NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [U10HL069294] Funding Source: NIH RePORTER

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Patients with follicular lymphoma (FL) experiencing early therapy failure (ETF) within 2 years of frontline chemoimmunotherapy have poor overall survival (OS). We analyzed data from the Center for International Blood and Marrow Transplant Research (CIBMTR) and the National LymphoCare Study (NLCS) to determine whether autologous hematopoietic cell transplant (autoHCT) can improve outcomes in this high-risk FL subgroup. ETF was defined as failure to achieve at least partial response after frontline chemoimmunotherapy or lymphoma progression within 2 years of frontline chemoimmunotherapy. We identified 2 groups: the nonautoHCT cohort (patients from the NLCS with ETF not undergoing autoHCT) and the autoHCT cohort (CIBMTR patients with ETF undergoing autoHCT). All patients received rituximab-based chemotherapy as frontline treatment; 174 non-autoHCT patients and 175 autoHCT patients were identified and analyzed. There was no difference in 5-year OS between the 2 groups (60% versus 67%, respectively; P = .16). A planned subgroup analysis showed that patients with ETF receiving autoHCT soon after treatment failure (<= 1 year of ETF; n = 123) had higher 5-year OS than those without autoHCT (73% versus 60%, P = .05). On multivariate analysis, early use of autoHCT was associated with significantly reduced mortality (hazard ratio, .63; 95% confidence interval, .42 to .94; P= .02). Patients with FL experiencing ETF after frontline chemoimmunotherapy lack optimal therapy. We demonstrate improved OS when receiving autoHCT within 1 year of treatment failure. Results from this unique collaboration between the NLCS and CIBMTR support consideration of early consolidation with autoHCT in select FL patients experiencing ETF. (C) 2017 American Society for Blood and Marrow Transplantation.

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