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Published on: May 27, 2011
The Hematopoietic Cell Transplant Comorbidity Index predicts survival after allogeneic transplant for nonmalignant
Monica S Thakar1, Larisa Broglie1, Brent Logan2
1Division of Pediatric Hematology, Oncology, and Blood and Marrow Transplantation, Department of Pediatrics, and.
Insights
The HCT Comorbidity Index (HCT-CI) predicts survival after allogeneic hematopoietic cell transplantation (HCT) for nonmalignant diseases. Higher HCT-CI scores (≥3) indicate inferior survival, except in hemoglobinopathy patients.
Area of Science:
- Hematology
- Transplantation Medicine
- Clinical Outcomes Research
Background:
- Mortality after allogeneic hematopoietic cell transplantation (HCT) for nonmalignant conditions remains a challenge.
- Pre-transplant patient conditions can significantly impact post-transplant survival outcomes.
Purpose of the Study:
- To evaluate the predictive value of the HCT Comorbidity Index (HCT-CI) for post-transplant survival in patients with nonmalignant diseases.
- To identify specific nonmalignant disease indications where HCT-CI may influence mortality risk.
Main Methods:
- Analysis of 4083 patients with nonmalignant diseases undergoing HCT between 2007-2014 from the Center for International Blood and Marrow Transplant Research database.
- Kaplan-Meier method for overall survival (OS) and multivariable Cox regression models to estimate hazard ratios (HRs) for HCT-CI scores.
- Stratification of analysis by disease indication to assess differential impact of HCT-CI on mortality.
Main Results:
- Increasing HCT-CI scores correlated with decreased 2-year OS: 82.7% (score 0), 80.3% (scores 1-2), 74% (scores 3-4), and 55.8% (score ≥5).
- HCT-CI scores of 3-4 (HR 1.33) and ≥5 (HR 2.31) significantly increased mortality risk compared to scores of 0-1.
- The HCT-CI's impact on mortality varied by disease: increased risk for aplastic anemia, immune deficiencies, and bone marrow failure syndromes, but not for hemoglobinopathies.
Conclusions:
- This large-scale study confirms that HCT-CI scores ≥3 are associated with inferior survival after HCT for most nonmalignant diseases, with hemoglobinopathies as a notable exception.
- The HCT-CI, alongside disease-specific factors, can aid in developing personalized treatment strategies and risk stratification for patients undergoing HCT for nonmalignant conditions.
Abstract:
Despite improvements, mortality after allogeneic hematopoietic cell transplantation (HCT) for nonmalignant diseases remains a significant problem. We evaluated whether pre-HCT conditions defined by the HCT Comorbidity Index (HCT-CI) predict probability of posttransplant survival. Using the Center for International Blood and Marrow Transplant Research database, we identified 4083 patients with nonmalignant diseases transplanted between 2007 and 2014. Primary outcome was overall survival (OS) using the Kaplan-Meier method. Hazard ratios (HRs) were estimated by multivariable Cox regression models. Increasing HCT-CI scores translated to decreased 2-year OS of 82.7%, 80.3%, 74%, and 55.8% for patients with HCT-CI scores of 0, 1 to 2, 3 to 4, and ≥5, respectively, regardless of conditioning intensity. HCT-CI scores of 1 to 2 did not differ relative to scores of 0 (HR, 1.12 [95% CI, 0.93-1.34]), but HCT-CI of 3 to 4 and ≥5 posed significantly greater risks of mortality (HR, 1.33 [95% CI, 1.09-1.63]; and HR, 2.31 [95% CI, 1.79-2.96], respectively). The effect of HCT-CI differed by disease indication. Patients with acquired aplastic anemia, primary immune deficiencies, and congenital bone marrow failure syndromes with scores ≥3 had increased risk of death after HCT. However, higher HCT-CI scores among hemoglobinopathy patients did not increase mortality risk. In conclusion, this is the largest study to date reporting on patients with nonmalignant diseases demonstrating HCT-CI scores ≥3 that had inferior survival after HCT, except for patients with hemoglobinopathies. Our findings suggest that using the HCT-CI score, in addition to disease-specific factors, could be useful when developing treatment plans for nonmalignant diseases.
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