The treatment versus experimentation dilemma in dose finding studies
From MaRDI portal
Publication:538132
DOI10.1016/j.jspi.2011.03.001zbMath1213.62167OpenAlexW1970342933MaRDI QIDQ538132
Yosef Rinott, Micha Mandel, David Azriel
Publication date: 23 May 2011
Published in: Journal of Statistical Planning and Inference (Search for Journal in Brave)
Full work available at URL: https://doi.org/10.1016/j.jspi.2011.03.001
Applications of statistics to biology and medical sciences; meta analysis (62P10) Optimal statistical designs (62K05) Medical applications (general) (92C50)
Related Items (14)
A note on continual reassessment method ⋮ Optimal sequential designs in phase I studies ⋮ Semiparametric Dose Finding Methods for Partially Ordered Drug Combinations ⋮ Response adaptive designs for phase II trials with binary endpoint based on context-dependent information measures ⋮ The role of minimal sets in dose finding studies ⋮ Optimal designs for contingent response models with application to toxicity-efficacy studies ⋮ Information in a two-stage adaptive optimal design ⋮ Performance Measures in Dose‐Finding Experiments ⋮ A continual reassessment method without undue risk of toxicity ⋮ A note on the robustness of the continual reassessment method ⋮ Adaptive clinical trial designs for phase I cancer studies ⋮ Adaptive Designs to Maximize Power in Clinical Trials with Multiple Treatments ⋮ Using Joint Utilities of the Times to Response and Toxicity to Adaptively Optimize Schedule–Dose Regimes ⋮ A conversation with Nancy Flournoy
Cites Work
- Unnamed Item
- Continual Reassessment Method: A Practical Design for Phase 1 Clinical Trials in Cancer
- Dose Finding for Continuous and Ordinal Outcomes with a Monotone Objective Function: A Unified Approach
- Approximate dynamic programming and its applications to the design of Phase I cancer trials
- A stochastic approximation by observations on a discrete lattice using isotonic regression
- Iterated least squares in multiperiod control
- Optimal Bayesian-feasible dose escalation for cancer phase I trials
- Cumulative cohort design for dose-finding
- Theoretical study of the continual reassessment method
- A Simple Technique to Evaluate Model Sensitivity in the Continual Reassessment Method
- Non-Parametric Up-and-down Experimentation
- Consistency of continual reassessment method under model misspecification
- A Curve‐Free Method for Phase I Clinical Trials
- A Method for Obtaining and Analyzing Sensitivity Data
This page was built for publication: The treatment versus experimentation dilemma in dose finding studies