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The Simplified Comorbidity Index: a new tool for prediction of nonrelapse mortality in allo-HCT
Roni Shouval1,2,3, Joshua A Fein4, Christina Cho1,3
1Adult Bone Marrow Transplant Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
Insights
A new Simplified Comorbidity Index (SCI) effectively predicts nonrelapse mortality (NRM) after allogeneic hematopoietic cell transplantation (allo-HCT). This index stratifies patients into distinct risk groups, outperforming the HCT-CI in validation studies.
Area of Science:
- Hematology
- Transplant Immunology
- Oncology
Background:
- Nonrelapse mortality (NRM) is a critical outcome following allogeneic hematopoietic cell transplantation (allo-HCT).
- Individual comorbidities significantly influence NRM, but their combined impact requires further elucidation.
Purpose of the Study:
- To investigate the individual and combined effects of comorbidities on NRM after allo-HCT.
- To develop and validate a novel comorbidity index for predicting NRM in allo-HCT recipients.
Main Methods:
- Analysis of a single-center cohort of 573 adult patients undergoing CD34-selected allo-HCT with myeloablative conditioning.
- Multivariable Cox regression to identify predictors of NRM.
- Development and validation of a Simplified Comorbidity Index (SCI) using identified predictors and an external cohort of 230 patients.
Main Results:
- Pulmonary disease, moderate-to-severe hepatic comorbidity, cardiac disease, and renal dysfunction were independently associated with increased NRM.
- The SCI, incorporating these comorbidities and age >60, stratified patients into 5 risk groups with NRM rates from 11.4% to 49.9%.
- The SCI demonstrated superior predictive performance (AUC 70.3-72.0) compared to the HCT-CI (AUC 61.7-65.7) in both development and validation cohorts.
Conclusions:
- A focused set of comorbidities, aggregated into the SCI, accurately predicts NRM after allo-HCT.
- The SCI effectively stratifies patients into distinct risk categories and offers improved discrimination over the HCT-CI.
- The SCI's validity in an external cohort supports its utility in clinical practice for risk assessment in allo-HCT patients.
Abstract:
Individual comorbidities have distinct contributions to nonrelapse mortality (NRM) following allogeneic hematopoietic cell transplantation (allo-HCT). We studied the impact of comorbidities individually and in combination in a single-center cohort of 573 adult patients who underwent CD34-selected allo-HCT following myeloablative conditioning. Pulmonary disease, moderate to severe hepatic comorbidity, cardiac disease of any type, and renal dysfunction were associated with increased NRM in multivariable Cox regression models. A Simplified Comorbidity Index (SCI) composed of the 4 comorbidities predictive of NRM, as well as age >60 years, stratified patients into 5 groups with a stepwise increase in NRM. NRM rates ranged from 11.4% to 49.9% by stratum, with adjusted hazard ratios of 1.84, 2.59, 3.57, and 5.38. The SCI was also applicable in an external cohort of 230 patients who underwent allo-HCT with unmanipulated grafts following intermediate-intensity conditioning. The area under the receiver operating characteristic curve (AUC) of the SCI for 1-year NRM was 70.3 and 72.0 over the development and external-validation cohorts, respectively; corresponding AUCs of the Hematopoietic Cell Transplantation-specific Comorbidity Index (HCT-CI) were 61.7 and 65.7. In summary, a small set of comorbidities, aggregated into the SCI, is highly predictive of NRM. The new index stratifies patients into distinct risk groups, was validated in an external cohort, and provides higher discrimination than does the HCT-CI.
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