4.2 Article

Transplantation Conditioning Regimens and Outcomes after Allogeneic Hematopoietic Cell Transplantation in Children and Adolescents with Acute Lymphoblastic Leukemia

Journal

BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION
Volume 19, Issue 2, Pages 255-259

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.bbmt.2012.09.019

Keywords

TBI dose; Leukemia recurrence

Funding

  1. Public Health Service Grant/Cooperative Agreement [U24-CA76518]
  2. National Cancer Institute, National Heart, Lung and Blood Institute
  3. National Institute of Allergy and Infectious Diseases [5U01HL069294]
  4. National Heart, Lung and Blood Institute and National Cancer Institute
  5. Health Resources and Services Administration [HHSH234200637015C]
  6. Office of Naval Research [N00014-06-1-0704, N00014-08-1-0058]
  7. Allos
  8. Amgen
  9. Angioblast
  10. Ariad
  11. Be the Match Foundation
  12. Blue Cross and Blue Shield Association
  13. Buchanan Family Foundation
  14. Caridian BCT
  15. Celgene
  16. Celgene, CellGenix
  17. Children's Leukemia Research Association
  18. Fresenius-Biotech North America
  19. Gamida Cell Teva Joint Venture
  20. Genentech
  21. Genzyme
  22. GlaxoSmithKline
  23. HistoGenetics
  24. Kiadis Pharma
  25. Medical College of Wisconsin
  26. Merck Co
  27. Millennium: Takeda Oncology
  28. Milliman USA
  29. Miltenyi Biotec
  30. National Marrow Donor Program
  31. Optum Healthcare Solutions
  32. Osiris Therapeutics
  33. Otsuka America Pharmaceutical
  34. RemedyMD
  35. Sanofi, Seattle Genetics
  36. Sigma-Tau Pharmaceuticals
  37. Soligenix
  38. StemCyte
  39. Stemsoft Software
  40. Swedish Orphan Biovitrum
  41. Tarix Pharmaceuticals
  42. Teva Neuroscience
  43. Therakos

Ask authors/readers for more resources

Relapse is common after hematopoietic stem cell transplantation (HSCT) for acute lymphoblastic leukemia (ALL). Although 1200 cGy total body irradiation (TBI) and cyclophosphamide (Cy) is the standard conditioning regimen, attempts to reduce relapse have led to the addition of a second chemotherapeutic agent and/or higher dose of TBI. We examined HSCT outcomes in patients age <18 years with ALL in second or subsequent remission or in relapse at transplantation. Most transplantations were performed with the patient in remission. Patients received grafts from an HLA-matched sibling or unrelated donor. Four treatment groups were created: (1) Cy + TBI <= 1200 cGy (n = 304), (2) Cy + etoposide + TBI <= 1200 cGy (n = 108), (3) Cy + TBI >= 1300 cGy (n = 327), and (4) Cy + etoPoside + TBI >= 1300 cGy (n = 26). Neither TBI > 1200 cGy nor the addition of etoposide resulted in fewer relapses. The 5-year probability of relapse was 30% for group 1, 28% for group 2, 35% for group 3, and 31% for group 4. However, transplantation-related mortality was higher (35% versus 25%, P = .02) and overall survival lower (36% versus 48%, P = .03) in group 4 compared with group 3. Our findings indicate that compared with the standard regimen, neither TBI > 1200 cGy nor the addition of etoposide improves survival after HSCT for ALL. (C) 2013 American Society for Blood and Marrow Transplantation.

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