Adaptive clinical trial designs for phase I cancer studies
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Publication:2452091
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- scientific article; zbMATH DE number 5032141
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Cites work
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- scientific article; zbMATH DE number 1361709 (Why is no real title available?)
- scientific article; zbMATH DE number 1361710 (Why is no real title available?)
- scientific article; zbMATH DE number 5224906 (Why is no real title available?)
- A Curve‐Free Method for Phase I Clinical Trials
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- A simple technique to evaluate model sensitivity in the continual reassessment method
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- Adaptive designs for dose-finding based on efficacy-toxicity response
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- Continual reassessment method for ordered groups
- Continual reassessment method for partial ordering
- Convergence properties of sequential Bayesian \(D\)-optimal designs
- Cumulative cohort design for dose-finding
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- Derivation of Exact Distributions Following an Up-and-Down Design
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- Designs for Single- or Multiple-Agent Phase I Trials
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- Dose-finding designs for HIV studies
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- THE DISTRIBUTION OF THE MAXIMUM LIKELIHOOD ESTIMATOR IN UP-AND-DOWN EXPERIMENTS FOR QUANTAL DOSE-RESPONSE DATA
- TWO-SAMPLE CONTINUAL REASSESSMENT METHOD
- The Continual Reassessment Method for Multiple Toxicity Grades: A Bayesian Quasi‐Likelihood Approach
- The treatment versus experimentation dilemma in dose finding studies
- Theoretical study of the continual reassessment method
- Toxicity in sequential dose-response experiments
- Two‐Dimensional Dose Finding in Discrete Dose Space
- Unifying CRM and EWOC designs for phase I cancer clinical trials
- Up-and-down experiments of first and second order
- Using joint utilities of the times to response and toxicity to adaptively optimize schedule-dose regimes
- Übersichtsarbeiten
Cited in
(21)- Adaptive Two-Stage Designs for Single-Arm Phase IIA Cancer Clinical Trials
- Bayesian adaptive two-stage design for determining person-time in phase II clinical trials with Poisson data
- Optimal adaptive two-stage designs for phase II cancer clinical trials
- A new design of the continual reassessment method
- Improving the flexibility and efficiency of phase II designs for oncology trials
- Motivating sample sizes in adaptive phase I trials via Bayesian posterior credible intervals
- Adaptive designs for phase II or III clinical trials for patients with cancer in Cuba
- Sequential methods in multi-arm clinical trials
- Statistical Properties of a Modified Accelerated Design for Phase I Cancer Clinical Trials
- Properties of adaptive clinical trial signature design in the presence of gene and gene-treatment interaction
- Adaptive decision making in a lymphocyte infusion trial
- On optimal designs for clinical trials: an updated review
- Adaptation in clinical development plans and adaptive clinical trial designs
- Performance Measures in Dose‐Finding Experiments
- A batch‐effect adjusted Simon's two‐stage design for cancer vaccine clinical studies
- Randomized phase II cancer clinical trials
- A continual reassessment method without undue risk of toxicity
- A Bayesian phase I/II trial design for immunotherapy
- Adaptive oncology Phase I trial design of drug combinations with drug-drug interaction modeling
- Bayesian models and decision algorithms for complex early phase clinical trials
- PA‐CRM: A continuous reassessment method for pediatric phase I oncology trials with concurrent adult trials
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