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Expanded HCT-CI Definitions Capture Comorbidity Better for Younger Patients of Allogeneic HCT for Nonmalignant
Larisa Broglie1, Brian D Friend2, Saurabh Chhabra3
1CIBMTR (Center for International Blood and Marrow Transplant Research), Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin; Division of Pediatric Hematology/Oncology/Blood and Marrow Transplant, Department of Pediatrics, Medical College of Wisconsin, Milwaukee, Wisconsin.
Insights
Modifying the Hematopoietic Cell Transplantation Comorbidity Index (HCT-CI) improves risk assessment for pediatric and young adult patients undergoing HCT for nonmalignant conditions. This expanded index better captures comorbidities, leading to more accurate mortality risk predictions in this population.
Area of Science:
- Pediatric Hematology
- Transplant Immunology
- Clinical Risk Stratification
Background:
- Allogeneic hematopoietic cell transplantation (HCT) offers cures for nonmalignant conditions but carries risks.
- The HCT Comorbidity Index (HCT-CI) aids mortality risk estimation but is underutilized in pediatric care.
- Existing HCT-CI lacks specificity for pediatric and adolescent/young adult (AYA) populations.
Purpose of the Study:
- To adapt and validate the HCT-CI for pediatric and AYA patients with nonmalignant diseases.
- To create an expanded HCT-CI (expanded ynHCT-CI) inclusive of pediatric-specific comorbidities.
- To improve the accuracy of transplant mortality risk assessment in younger HCT recipients.
Main Methods:
- Utilized the Center for International Blood and Marrow Transplant Research database (2815 pediatric/AYA patients, 2008-2017).
- Expanded HCT-CI definitions to include mechanical ventilation, invasive fungal infections, chronic kidney disease (CKD), obesity, and underweight.
- Developed an expanded youth nonmalignant HCT-CI (expanded ynHCT-CI) and a simplified version.
Main Results:
- Expanded comorbidities like mechanical ventilation (9.6%), fungal infections (5.9%), and CKD (14.3% total) were frequent.
- 39% of patients experienced an increased comorbidity score with the expanded ynHCT-CI.
- An increased comorbidity score correlated with a higher mortality hazard (HR=1.41).
Conclusions:
- Modifications to the HCT-CI are crucial for accurately assessing risk in pediatric and AYA nonmalignant HCT patients.
- The expanded ynHCT-CI provides a more clinically relevant risk assessment tool for this population.
- Improved comorbidity capture enhances the utility of HCT-CI in younger patients.
Abstract:
Allogeneic hematopoietic cell transplantation (HCT) can cure many nonmalignant conditions, but concern for morbidity and mortality remains. To help physicians estimate patient-specific transplant mortality risk, the HCT comorbidity index (HCT-CI) is used. However, pediatric physicians use the HCT-CI less frequently than adult counterparts. We used the Center for International Blood and Marrow Transplant Research database to expand the HCT-CI comorbidity definitions to be more inclusive of children and adolescent and young adult (AYA) patients, adding history of mechanical ventilation, history of invasive fungal infection, assessment of chronic kidney disease (CKD) by estimated glomerular filtration rate, expanding the definition of obesity, and adding an underweight category. A total of 2815 children and AYAs (<40 years old) who received first allogeneic HCT for nonmalignant diseases from 2008 to 2017 were included to create an expanded youth nonmalignant HCT-CI (expanded ynHCT-CI) and a simplified non-malignant (simplified ynHCT-CI) HCT-CI. The expanded comorbidities occurred frequently-history of mechanical ventilation (9.6%), history of invasive fungal infection (5.9%), mild CKD (12.2%), moderate/severe CKD (2.1%), obesity (10.9%), and underweight (14.5%). Thirty-nine percent of patients had an increase in their comorbidity score using the expanded ynHCT-CI, leading to a redistribution of scores: ynHCT-CI score 0 (35%), 1-2 (36.4%), and ≥3 (28.6%). Patients with an increase in their comorbidity score had an increased hazard of mortality compared to those whose score remained the same (hazard ratio = 1.41; 95% confidence interval, 1.01-1.98). Modifications to the HCT-CI can benefit children and AYA patients with nonmalignant diseases, creating a risk assessment tool that is clinically relevant and better captures comorbidity in this younger population.
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