Dose finding with longitudinal data: simpler models, richer outcomes
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Cites work
- A simple technique to evaluate model sensitivity in the continual reassessment method
- Consistency of continual reassessment method under model misspecification
- Continual Reassessment Method: A Likelihood Approach
- Continual Reassessment Method: A Practical Design for Phase 1 Clinical Trials in Cancer
- Design efficiency in dose finding studies
- Dose-Finding Based on Efficacy-Toxicity Trade-Offs
- Dose-finding design using mixed-effect proportional odds model for longitudinal graded toxicity data in phase I oncology clinical trials
- Dose-finding designs using a novel quasi-continuous endpoint for multiple toxicities
- Miscellanea. A stopping rule for the continual reassessment method
- Models for discrete longitudinal data.
- Sequential Designs for Phase I Clinical Trials with Late‐Onset Toxicities
- Small-Sample Confidence Sets for the MTD in a Phase I Clinical Trial
- Statistical Methods for Dose‐Finding Experiments
- The Continual Reassessment Method for Multiple Toxicity Grades: A Bayesian Quasi‐Likelihood Approach
- Utility-Based Optimization of Combination Therapy Using Ordinal Toxicity and Efficacy in Phase I/II Trials
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