Using Joint Utilities of the Times to Response and Toxicity to Adaptively Optimize Schedule–Dose Regimes
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Publication:2861956
DOI10.1111/biom.12065zbMath1429.62616OpenAlexW1556099520WikidataQ38428895 ScholiaQ38428895MaRDI QIDQ2861956
Peter F. Thall, Thomas M. Braun, Hoang Q. Nguyen, Muzaffar H. Qazilbash
Publication date: 13 November 2013
Published in: Biometrics (Search for Journal in Brave)
Full work available at URL: http://europepmc.org/articles/pmc3963428
Applications of statistics to biology and medical sciences; meta analysis (62P10) Medical applications (general) (92C50)
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Cites Work
- Continual Reassessment Method: A Practical Design for Phase 1 Clinical Trials in Cancer
- Dose-Finding Based on Efficacy-Toxicity Trade-Offs
- The treatment versus experimentation dilemma in dose finding studies
- Bayesian models and decision algorithms for complex early phase clinical trials
- Optimizing the Concentration and Bolus of a Drug Delivered by Continuous Infusion
- Monitoring late-onset toxicities in phase I trials using predicted risks
- A Strategy for Dose-Finding and Safety Monitoring Based on Efficacy and Adverse Outcomes in Phase I/II Clinical Trials
- Sequential Designs for Phase I Clinical Trials with Late‐Onset Toxicities
- Determining a Maximum‐Tolerated Schedule of a Cytotoxic Agent