Influence of comorbidities on outcome in 1102 patients with an allogeneic hematopoietic stem cell transplantation
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Published on: March 17, 2020
Marie Janscak1,2, Anne Stelmes1,2, Jana van den Berg1,2
1Division of Hematology, University Hospital Basel, Basel, Switzerland.
Insights
The Hematopoietic Comorbidity Risk Index (HCT-CI) shows significant differences in non-relapse mortality (NRM) for low-risk patients undergoing allogeneic hematopoietic stem cell transplantation (allo-HSCT). Cardiac disease is a key predictor of NRM and overall survival.
Area of Science:
- Hematology
- Transplant Immunology
- Oncology
Background:
- The Hematopoietic Comorbidity Risk Index (HCT-CI) is a standard tool for assessing pre-transplant comorbidities in allogeneic hematopoietic stem cell transplantation (allo-HSCT).
- Advances in HSCT techniques and supportive care necessitate re-evaluation of the HCT-CI's predictive accuracy over time.
- Previous studies established HCT-CI's utility in predicting non-relapse mortality (NRM).
Purpose of the Study:
- To re-evaluate the predictive value of the HCT-CI in a contemporary cohort of allo-HSCT patients.
- To assess the impact of specific comorbidities, particularly cardiac disease, on transplant outcomes.
- To identify factors influencing NRM and overall survival (OS) in patients undergoing allo-HSCT.
Main Methods:
- Retrospective analysis of 1102 consecutive patients undergoing allo-HSCT between 2006 and 2021.
- Patients were stratified into low (HCT-CI 0), intermediate (HCT-CI 1-2), and high-risk (HCT-CI ≥3) groups.
- Multivariate analysis was used to assess the association of HCT-CI, organ subgroups, donor type, disease status, and prior HSCT with NRM and OS.
Main Results:
- At 10 years, NRM was 21.0% (low), 26.0% (intermediate), and 25.8% (high-risk), with a significant difference between low and intermediate groups (p<0.001).
- Overall survival at 10 years was 49.9% (low), 39.8% (intermediate), and 31.1% (high-risk) (p<0.001).
- Cardiac disease was the strongest predictor of NRM (HR=1.73, p=0.02) and OS (HR=1.77, p<0.001). Unrelated/mismatched related donors, advanced disease, and prior HSCT also impacted NRM.
Conclusions:
- The HCT-CI remains a valuable tool, particularly in distinguishing low-risk patients, but its predictive power for intermediate vs. high-risk groups may be diminishing.
- Cardiac disease is a critical comorbidity impacting allo-HSCT outcomes, warranting closer attention.
- Improvements in transplant procedures and supportive care may be mitigating the impact of certain comorbidities on NRM.
Abstract:
The hematopoietic comorbidity risk index (HCT-CI) is a pre-transplant risk assessment tool used to qualify comorbidities to predict non-relapse mortality (NRM) of patients undergoing allogeneic hematopoietic stem cell transplantation (allo-HSCT). HSCT procedures continue to improve. Therefore, the predictive value of HCT-CI needs to be re-evaluated. Our study is a retrospective analysis of pre-existing comorbidities assessing the relevance of the HCT-CI on the outcome of consecutive patients (n = 1102) undergoing allo-HSCT from 2006-2021. HCT-CI was classified as low (HCT-CI 0), intermediate (HCT-CI 1-2) and high-risk (HCT-CI ≥ 3). At 10 years, NRM for low, intermediate, and high-risk HCT-CI group was 21.0%, 26.0%, and 25.8% (p = 0.04). NRM difference was significant between low to intermediate (p < 0.001), but not between intermediate to high-risk HCT-CI (p = 0.22). Overall survival (OS) at 10 years differed significantly with 49.9%, 39.8%, and 31.1%, respectively (p < 0.001). In multivariate analysis of HCT-CI organ subgroups, cardiac disease was most strongly associated with NRM (HR = 1.73, p = 0.02) and OS (HR = 1.77, p < 0.001). All other individual organ comorbidities influenced NRM to a lesser extent. Further, donor (HR = 2.20, p < 0.001 for unrelated and HR = 2.17, p = 0.004 for mismatched related donor), disease status (HR = 1.41, p = 0.03 for advanced disease) and previous HSCT (HR = 1.55, p = 0.009) were associated with NRM. Improvement in transplant techniques and supportive care may have improved outcome with respect to comorbidities.
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