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.

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