4.2 Article

Allogeneic Transplantation to Treat Therapy-Related Myelodysplastic Syndrome and Acute Myelogenous Leukemia in Adults

期刊

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jtct.2021.08.010

关键词

Allogeneic transplantation; Acute myelogenous leukemia; Myelodysplasia

资金

  1. Public Health Service [U24CA076518]
  2. National Cancer Institute (NCI)
  3. National Heart, Lung and Blood Institute (NHLBI)
  4. National Institute of Allergy and Infectious Diseases (NIAID)
  5. NHLBI [OT3HL147741, R21 HL140314, U01HL128568, R01 HL131731, R01 HL126589, U24HL138660]
  6. NCI [U24CA233032]
  7. Health Resources and Services Administration (HRSA) [HHSH250201700006C]
  8. Office of Naval Research [N00014-18-1-2888, N00014-17-1-2850]
  9. HRSA [SC1MC31881-01-00]
  10. NIH [5P01CA111412, 5R01HL129472, R01CA152108, 1R01HL131731, 1U01AI126612, 1R01CA231141]
  11. Actinium Pharmaceuticals
  12. Adaptive Biotechnologies
  13. Amgen
  14. Allovir

向作者/读者索取更多资源

The prognosis for patients with therapy-related myeloid neoplasm, including myelodysplastic syndrome (t-MDS) and acute myelogenous leukemia (t-AML), is poor. Although modern supportive care and conditioning regimens have improved outcomes, the major cause of treatment failure remains relapse. Caution is advised when recommending allogeneic hematopoietic cell transplantation, and more effective antineoplastic approaches are needed.
Patients who develop therapy-related myeloid neoplasm, either myelodysplastic syndrome (t-MDS) or acute myelogenous leukemia (t-AML), have a poor prognosis. An earlier Center for International Blood and Marrow Transplant Research (CIBMTR) analysis of 868 allogeneic hematopoietic cell transplantations (allo-HCTs) performed between 1990 and 2004 showed a 5-year overall survival (OS) and disease-free survival (DFS) of 22% and 21%, respectively. Modern supportive care, graft-versus-host disease prophylaxis, and reduced-intensity conditioning (RIC) regimens have led to improved outcomes. Therefore, the CIBMTR analyzed 1531 allo-HCTs performed in adults with t-MDS (n = 759) or t-AML (n = 772) between and 2000 and 2014. The median age was 59 years (range, 18 to 74 years) for the patients with t-MDS and 52 years (range, 18 to 77 years) for those with tAML. Twenty-four percent of patients with t-MDS and 11% of those with t-AML had undergone a previous autologous (auto-) HCT. A myeloablative conditioning (MAC) regimen was used in 49% of patients with t-MDS and 61% of patients with t-AML. Nonrelapse mortality at 5 years was 34% (95% confidence interval [CI], 30% to 37%) for patients with t-MDS and 34% (95% CI, 30% to 37%) for those with t-AML. Relapse rates at 5 years in the 2 groups were 46% (95% CI, 43% to 50%) and 43% (95% CI, 40% to 47%). Five-year OS and DFS were 27% (95% CI, 23% to 31%) and 19% (95% CI, 16% to 23%), respectively, for patients with t-MDS and 25% (95% CI, 22% to 28%) and 23% (95% CI, 20% to 26%), respectively, for those with t-AML. In multivariate analysis, OS and DFS were significantly better in young patients with low-risk t-MDS and those with t-AML undergoing HCT with MAC while in first complete remission, but worse for those with previous auto-HCT, higher-risk cytogenetics or Revised International Prognostic Scoring System score, and a partially matched unrelated donor. Relapse remains the major cause of treatment failure, with little improvement seen over the past 2 decades. These data mandate caution when recommending allo-HCT in these conditions and indicate the need for more effective antineoplastic approaches before and after allo-HCT. (C) 2021 Published by Elsevier Inc. on behalf of The American Society for Transplantation and Cellular Therapy.

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