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Using conditional logistic regression to fit proportional odds models to interval censored data
D Rabinowitz1, R A Betensky, A A Tsiatis
1Department of Statistics, Columbia University, New York, New York 10027, USA. dan@wald.stat.columbia.edu
Biometrics
|July 6, 2000
Summary
A new method simplifies proportional odds regression for interval-censored data using standard conditional logistic regression. This approach accurately models time-to-event data, including in AIDS clinical trials.
Area of Science:
- Biostatistics
- Survival Analysis
- Epidemiology
Background:
- Interval-censored data presents unique challenges in statistical modeling.
- Proportional odds regression is a valuable tool for analyzing such data.
- Existing methods for fitting proportional odds models to interval-censored data can be complex.
Purpose of the Study:
- To present an easily implemented approach for fitting the proportional odds regression model to interval-censored data.
- To demonstrate the applicability of the method for both interval-censored and current status data.
- To assess the accuracy of the proposed methodology through simulations.
Main Methods:
- The proposed approach utilizes conditional logistic regression routines available in standard statistical packages.
- This method bypasses complexities associated with estimating the baseline odds ratio function.
- The methodology is illustrated using data from an AIDS study comparing combination therapy (ZDV+ddC) versus ZDV alone.
Main Results:
- The conditional logistic regression approach provides a practical solution for fitting proportional odds models to interval-censored data.
- The method is shown to be applicable in various data settings, including ongoing examinations.
- Simulations indicate the procedure is accurate for assessing treatment effects, such as on CD4 cell count changes.
Conclusions:
- The presented approach offers a straightforward and effective way to fit proportional odds regression models for interval-censored data.
- This method enhances the analysis of time-to-event data in epidemiological and clinical studies.
- The use of standard statistical software makes this approach accessible to a wider range of practitioners.