AI Article Synopsis

  • The study examined how the hematopoietic cell transplantation-comorbidity index (HCT-CI) and its age-adjusted version (HCT-CI/age) relate to transplant outcomes in patients with acute myeloid leukemia and myelodysplastic syndrome undergoing allogeneic HCT with CD34-selected grafts.
  • Higher scores on both indices were associated with increased nonrelapse mortality and decreased overall survival, with the HCT-CI defining two distinct risk groups, while the HCT-CI/age showed a progressive risk increase across four categories.
  • Both models demonstrated effective predictive accuracy for nonrelapse mortality, suggesting they could help in selecting appropriate patients for allogeneic HCT.

Article Abstract

To evaluate the association between the hematopoietic cell transplantation-comorbidity index (HCT-CI) and the recently developed age-adjusted HCT-CI (HCT-CI/age) and transplant outcomes in the setting of CD34-selected allogeneic HCT, we analyzed a homogeneous population of patients undergoing allogeneic HCT with CD34-selected grafts for acute myeloid leukemia and myelodysplastic syndrome (n = 346). Median HCT-CI and HCT-CI/age scores were 2 (percentile 25 to 75, 1 to 4) and 3 (percentile 25 to 75, 1 to 5), respectively. Higher HCT-CI and HCT-CI/age scores were associated with higher nonrelapse mortality (NRM) and lower overall survival (OS). The HCT-CI distinguished 2 risk groups (0 to 2 versus ≥3), whereas, with the HCT-CI/age, there was a progressive increase in NRM and decrease in OS with increasing scores in all 4 groups (0 versus 1 to 2 versus 3 to 4 versus ≥5). Higher scores in both models were associated with lower chronic graft-versus-host disease relapse-free survival but not with higher relapse. Both models showed a promising predictive accuracy for NRM (c- = .616 for HCT-CI and c- = .647 for HCT-CI/age). In conclusion, the HCT-CI and HCT-CI/age predict transplant outcomes in CD34-selected allo-HCT, including NRM, OS, and chronic graft-versus-host disease relapse-free survival and may be used to select appropriate patients for this approach.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5182101PMC
http://dx.doi.org/10.1016/j.bbmt.2016.10.017DOI Listing

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