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Updated: Feb 15, 2026

Isolation and Transplantation of Hematopoietic Stem Cells HSCs
Published on: February 25, 2007
Age adjusted hematopoietic stem cell transplant comorbidity index predicts survival in a T-cell depleted cohort
Hayder Saeed1, Swati Yalamanchi1, Meng Liu2
1Division of Hematology and Blood and Marrow Transplant, Markey Cancer Center, University of Kentucky, United States.
Insights
The updated comorbidity index (HCT-CI/Age) better predicts survival after allogeneic hematopoietic stem cell transplant (HCT) compared to the pre-transplant assessment of mortality (PAM) score. This improved risk stratification aids in selecting appropriate candidates for HCT.
Area of Science:
- Hematology
- Transplant Immunology
- Oncology
Background:
- Allogeneic hematopoietic stem cell transplant (HCT) is a complex procedure with evolving indications.
- Accurate risk stratification is crucial for patient selection, especially in higher-risk populations.
- Existing risk assessment tools require continuous validation and updates.
Purpose of the Study:
- To evaluate the performance of the new comorbidity index (HCT-CI/Age) in predicting outcomes after allogeneic HCT.
- To compare the predictive accuracy of HCT-CI/Age against the pre-transplant assessment of mortality (PAM) score.
- To determine the utility of HCT-CI/Age in identifying patients who may benefit from alternative treatment strategies.
Main Methods:
- Retrospective analysis of 114 adult patients undergoing allogeneic HCT.
- Utilized Kaplan-Meier curves, log-rank tests, Cox models, and Pearson correlation for analysis.
- Compared the predictive capabilities of HCT-CI/Age and PAM scores for overall survival and non-relapse mortality.
Main Results:
- HCT-CI/Age scores were positively correlated with mortality risk (correlation coefficient 0.43, p < 0.001).
- HCT-CI/Age accurately predicted 2-year overall survival and non-relapse mortality in distinct risk groups (p=0.004, p=0.003).
- PAM score did not significantly differentiate outcomes between low and high-risk groups (p=0.19).
Conclusions:
- The HCT-CI/Age index demonstrates superior discriminative ability compared to PAM for predicting outcomes in allogeneic HCT recipients.
- This enhanced risk stratification can guide clinical decisions, potentially identifying patients for intensified management or alternative therapies.
- Further validation in larger cohorts is warranted, but HCT-CI/Age shows promise for optimizing HCT candidate selection.
Objectives:
Allogeneic hematopoietic stem cell transplant (HCT) continues to evolve with the treatment in higher risk patient population. This practice mandates stringent update and validation of risk stratification prior to undergoing such a complex and potentially fatal procedure. We examined the adoption of the new comorbidity index (HCT-CI/Age) proposed by the Seattle group after the addition of age variable and compared it to the pre-transplant assessment of mortality (PAM) that already incorporates age as part of its evaluation criteria.
Methods:
A retrospective analysis of adult patients who underwent HCT at our institution from January 2010 through August 2014 was performed. Kaplan-Meier's curve, log-rank tests, Cox model and Pearson correlation was used in the analysis.
Results:
Of the 114 patients that underwent allogeneic transplant in our institution, 75.4% were ≥40 years old. More than 58% had a DLCO ≤80%. Although scores were positively correlated (correlation coefficient 0.43, p < 0.001), HCT-CI/Age more accurately predicted 2-year overall survival (OS) and non-relapse mortality (NRM) in patients with lower (0-4) and higher (5-7) scores (52% and 36% versus 24% and 76%, p = 0.004, 0.003 respectively). PAM score did not reach statistical significance for difference in OS nor NRM between the low (<24) and high-risk (≥24) groups (p = 0.19 for both).
Conclusions:
Despite our small sample population, HCT-CI/Age was more discriminative to identify patients with poor outcome that might benefit from intensified management strategies or other therapeutic approaches rather than allogeneic HCT.
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