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A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
A drug comorbidity index to predict mortality in men with castration resistant prostate cancer
Giuseppe Fallara1,2,3, Rolf Gedeborg3, Anna Bill-Axelson3
1Division of Experimental Oncology/Unit of Urology URI, IRCCS Ospedale San Raffaele, Milan, Italy.
Insights
A new drug comorbidity index (DCI-CRPC) using prescription data predicts mortality in castration resistant prostate cancer (CRPC) patients better than the Charlson Comorbidity Index, improving prognostic accuracy.
Area of Science:
- Oncology
- Epidemiology
- Pharmacology
Background:
- The Charlson Comorbidity Index (CCI) has limitations in predicting mortality for men with castration resistant prostate cancer (CRPC).
- A novel comorbidity index, the drug comorbidity index (DCI-CRPC), was developed using filled prescription data for improved prognostic accuracy in CRPC patients.
- This index is designed for use in registry-based studies.
Purpose of the Study:
- To develop and validate a new comorbidity index (DCI-CRPC) for predicting mortality in men with castration resistant prostate cancer (CRPC).
- To compare the predictive performance of the DCI-CRPC against the Charlson Comorbidity Index (CCI) and an original DCI in a population-based cohort.
Main Methods:
- A population-based cohort of 1,885 men with CRPC was analyzed.
- The drug comorbidity index (DCI-CRPC) was calculated based on prescriptions filled within 365 days prior to CRPC diagnosis.
- Mortality prediction was assessed using Kaplan-Meier curves and compared with CCI and original DCI via univariable models and C-indices.
Main Results:
- The DCI-CRPC demonstrated superior discriminative ability (C-index 0.667) compared to the Charlson Comorbidity Index (C-index 0.508).
- Median overall survival varied significantly across DCI-CRPC tertiles, from 3.0 years to 1.0 year.
- The DCI-CRPC showed comparable performance to the original DCI and its discriminative ability was highest in less aggressive cancer subgroups.
Conclusions:
- The newly developed drug comorbidity index (DCI-CRPC) effectively predicts mortality in men with castration resistant prostate cancer (CRPC).
- The DCI-CRPC offers improved prognostic accuracy over the Charlson Comorbidity Index for CRPC patients.
- This prescription-based index is a valuable tool for registry-based studies in oncology.
Background:
The Charlson Comorbidity Index is a poor predictor of mortality in men with castration resistant prostate cancer (CRPC). To improve this prediction, we created a comorbidity index based on filled prescriptions intended to be used in registry-based studies.
Materials And Methods:
In a population-based cohort of men with CPRC a drug comorbidity index (DCI-CRPC) was calculated based on prescriptions filled during a 365-day period before the date of CRPC diagnosis to predict mortality. Five risk categories for men with CRPC were defined based on PSA kinetics. Mortality rates were described by Kaplan-Meier curves. The predictive ability of the DCI-CRPC was compared in univariable models to that of the original DCI, derived from men in the general population, and to that of the Charlson Comorbidity Index.
Results:
In 1,885 men with CRPC the median overall survival ranged from 3.0 years (95% confidence interval [CI] 2.8 to 3.4) in the first tertile of the DCI-CRPC, to 1.0 year (95% CI 0.9 to 1.1) in the third tertile of the DCI-CRPC. The index had higher discriminative ability (C-index 0.667) than the Charlson Comorbidity Index (C-index 0.508). The discriminative ability of the DCI-CRPC was highest in the subgroup with least aggressive cancer (C-index 0.651) and lowest in men with most aggressive cancer (C-index 0.618). The performance of the DCI-CRPC was comparable to that of the original DCI.
Conclusion:
Our newly created comorbidity index using filled prescriptions predicted death in men with CRPC better than the Charlson Comorbidity Index.
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