4.2 Article

Chronic Graft-versus-Host Disease, Nonrelapse Mortality, and Disease Relapse in Older versus Younger Adults Undergoing Matched Allogeneic Peripheral Blood Hematopoietic Cell Transplantation: A Center for International Blood and Marrow Transplant Research Analysis

Journal

TRANSPLANTATION AND CELLULAR THERAPY
Volume 28, Issue 1, Pages 34-42

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jtct.2021.10.002

Keywords

Allogeneic Hematopoietic Cell; Transplantation; Older Adults; Chronic Graft-Versus-Host; Disease; Non-Relapse Mortality; Relapse

Funding

  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) [HHSH250201700006C]
  5. Health Resources and Services Administration (HRSA) [N00014-20-1-2705, N00014-20-1-2832]
  6. Office of Naval Research
  7. Match Foundation
  8. Medical College of Wisconsin
  9. National Marrow Donor Program
  10. Adaptive Biotechnologies, Adienne SA
  11. Astellas Pharma US, bluebird bio, Bristol Myers Squibb
  12. CareDx
  13. Fate Therapeutics
  14. Karyopharm Therapeutics
  15. Kiadis Pharma
  16. Kite Pharma
  17. Kyowa Kirin
  18. Magenta Therapeutics
  19. Medac
  20. Takeda Pharmaceuticals
  21. Xenikos BV

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In this study, the effect of chronic graft-versus-host disease (cGVHD) on nonrelapse mortality (NRM) and relapse risk was investigated in older adults undergoing allogeneic hematopoietic cell transplantation. The results revealed that cGVHD significantly increased the risk of NRM and decreased the risk of relapse, regardless of age. Older adults had a higher risk of NRM, but the impact of cGVHD on NRM did not differ based on age.
The effect of chronic graft-versus-host disease (cGVHD) on the risk of nonrelapse mortality (NRM) and relapse has not been specifically studied in older adults, who are increasingly undergoing allogeneic hematopoietic cell transplantation (alloHCT) and surviving long-term to develop cGVHD. In this Center for International Blood and Marrow Transplant Research (CIBMTR) analysis, we tested our hypothesis that the risk of NRM was higher with the development of cGVHD, particularly among older adults (age > 60 years). We included 4429 adults age > 40 years who underwent a first HLA-matched peripheral blood stem cell alloHCT for acute myelogenous leukemia or myelodysplastic syndrome between 2008 and 2017. We compared outcomes of 4 groups & mdash;older adults (> 60 years) and younger adults (40 to 59 years) with cGVHD and older and younger adults without cGVHD & mdash;to determine the effect of older age and cGVHD on various outcomes. We used Cox proportional hazard models to determine the risk of NRM, relapse, and overall survival (OS). We treated cGVHD as a time-dependent covariate. The severity of cGVHD was based on the CIBMTR clinical definitions. cGVHD was significantly associated with a higher risk of NRM and lower risk of relapse regardless of age. The risk of NRM was higher for older adults versus younger adults. Adults who developed cGVHD as a group had longer OS compared with age-matched cohorts without cGVHD. Older adults had worse OS regardless of cGVHD. Among adults with cGVHD, clinically moderate or severe cGVHD was associated with a significantly higher risk of NRM and lower risk of relapse; severe cGVHD was associated with shorter OS, whereas mild to moderate cGVHD was associated with longer OS. Among both younger and older adults, the development of cGVHD was associated with a higher risk of NRM, lower risk of relapse, and longer OS. Older adults had a higher risk of NRM, but the increased risk of NRM associated with cGVHD did not differ based on age. The development of mild to moderate cGVHD offered the most favorable balance between minimizing NRM and decreasing the risk of relapse. The relapse risk was lowest for adults with severe cGVHD, but high NRM resulted in shorter OS. Developing strategies to avoid clinically severe cGVHD is critically important. (c) 2021 American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. (c) 2021 The American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. All rights reserved.

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