Abstract
Older age and a high burden of comorbidities often drive the selection of low-intensity conditioning regimens in allogeneic hematopoietic stem cell transplantation recipients. However, the impact of comorbidities in the low-intensity conditioning setting is unclear. We sought to determine the contribution of individual comorbidities and their cumulative burden on the risk of nonrelapse mortality (NRM) among patients receiving low-intensity regimens. In a retrospective analysis of adults (≥18 years) who underwent transplantation for acute myeloid leukemia in the first complete remission between 2008 and 2018, we studied recipients of low-intensity regimens as defined by the transplantation conditioning intensity (TCI) scale. Multivariable Cox models were constructed to study associations of comorbidities with NRM. Comorbidities identified as putative risk factors in the low-TCI setting were included in combined multivariable regression models assessed for overall survival, NRM, and relapse. A total of 1663 patients with a median age of 61 years received low-TCI regimens. Cardiac comorbidity (including arrhythmia/valvular disease) and psychiatric disease were associated with increased NRM risk (hazard ratio [HR], 1.54; 95% confidence interval [CI], 1.13-2.09 and HR, 1.69; 95% CI, 1.02-2.82, respectively). Moderate pulmonary dysfunction, though prevalent, was not associated with increased NRM. In a combined model, cardiac, psychiatric, renal, and inflammatory bowel diseases were independently associated with adverse transplantation outcomes. These findings may inform patient and regimen selection and reinforce the need for further investigation of cardioprotective transplantation approaches.
Original language | English |
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Pages (from-to) | 2143-2152 |
Number of pages | 10 |
Journal | Blood advances |
Volume | 7 |
Issue number | 10 |
DOIs | |
State | Published - 23 May 2023 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2023 by The American Society of Hematology.
Funding
The authors thank the data managers for their excellent work and the patients who provided data. They also thank all of the European Society for Blood and Marrow Transplantation centers and national registries for contributing patients to this study (supplemental Appendix). This work is supported by funding and a grant from the American Society for Hematology HONORS award (J.A.F.) and the Memorial Sloan Kettering Cancer Center Core grant, National Cancer Institute, National Institutes of Health (grant P30 CA008748) (R.S.).
Funders | Funder number |
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American Society for Hematology | |
National Institutes of Health | P30 CA008748 |
National Cancer Institute |