Adaptive clinical trial designs for phase I cancer studies (Q2452091): Difference between revisions

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+Cumulative cohort design for dose-finding
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+Continual Reassessment Method: A Practical Design for Phase 1 Clinical Trials in Cancer
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+Optimal Bayesian-feasible dose escalation for cancer phase I trials
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+The treatment versus experimentation dilemma in dose finding studies
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+Übersichtsarbeiten
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+Optimal Design for Nonlinear Response Models
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+Approximate dynamic programming and its applications to the design of Phase I cancer trials
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+Incorporating Individual and Collective Ethics into Phase I Cancer Trial Designs
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+Adaptive designs for dose-finding based on efficacy-toxicity response
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+Stochastic approximation and modern model-based designs for dose-finding clinical trials
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+Coherence principles in dose-finding studies
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+Statistical Methods for Dose‐Finding Experiments
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+Design and Analysis of Phase I Clinical Trials
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+Small-Sample Confidence Sets for the MTD in a Phase I Clinical Trial
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+Operating characteristics of the standard phase I clinical trial design.
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+Statistical properties of the traditional algorithm-based designs for phase I cancer clinical trials
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+Statistical Properties of a Modified Accelerated Design for Phase I Cancer Clinical Trials
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+Existence of three solutions to a second-order nonhomogeneous multipoint boundary-value problem
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+A Method for Obtaining and Analyzing Sensitivity Data
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+Toxicity in sequential dose-response experiments
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+A Random Walk Rule for Phase I Clinical Trials
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+Up-and-down experiments of first and second order
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+Asymptotic normality of maximum likelihood estimators from multiparameter response-driven designs
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+THE DISTRIBUTION OF THE MAXIMUM LIKELIHOOD ESTIMATOR IN UP-AND-DOWN EXPERIMENTS FOR QUANTAL DOSE-RESPONSE DATA
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+Properties of frequency distributions induced by general ''up-and-down'' methods for estimating quantiles
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+Dose Finding Using the Biased Coin Up-and-Down Design and Isotonic Regression
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+Derivation of Exact Distributions Following an Up-and-Down Design
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+Group up-and-down designs for dose-finding
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+Randomized group up and down experiments
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+A New Dose‐Finding Design for Bivariate Outcomes
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+Designs for Single- or Multiple-Agent Phase I Trials
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+Continual reassessment and related dose-finding designs
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+Continual Reassessment Method: A Likelihood Approach
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+Estimating the Probability of Toxicity at the Recommended Dose Following a Phase I Clinical Trial in Cancer
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+Consistency of continual reassessment method under model misspecification
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+Theoretical study of the continual reassessment method
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+A note on the robustness of the continual reassessment method
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+Non-parametric optimal design in dose finding studies
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+A Simple Technique to Evaluate Model Sensitivity in the Continual Reassessment Method
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+A Curve‐Free Method for Phase I Clinical Trials
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+Curve-Free and Model-Based Continual Reassessment Method Designs
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+On the Use of Nonparametric Curves in Phase I Trials with Low Toxicity Tolerance
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+A class of designs for Phase I cancer clinical trials combining Bayesian and likelihood approaches
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+Robust EM Continual Reassessment Method in Oncology Dose Finding
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+Phase I (or Phase II) Dose-Ranging Clinical Trials: Proposal of a Two-Stage Bayesian Design
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+Miscellanea. A stopping rule for the continual reassessment method
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+Continual reassessment designs with early termination
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+Sequential Designs for Phase I Clinical Trials with Late‐Onset Toxicities
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+Monitoring late-onset toxicities in phase I trials using predicted risks
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+TWO-SAMPLE CONTINUAL REASSESSMENT METHOD
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+Continual Reassessment Method for Ordered Groups
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+Designs foe phase i cancer clinical trials with differentiation of graded toxicity
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+The Continual Reassessment Method for Multiple Toxicity Grades: A Bayesian Quasi‐Likelihood Approach
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+Continual Reassessment Method for Partial Ordering
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+Dose-Finding Based on Feasibility and Toxicity in T-cell Infusion Trials
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+Dose-Finding Designs for HIV Studies
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+Dose finding with escalation with overdose control (EWOC) in cancer clinical trials
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+Incorporating a patient dichotomous characteristic in cancer phase I clinical trials using escalation with overdose control
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+Escalation with overdose control using ordinal toxicity grades for cancer phase I clinical trials
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+Number of patients per cohort and sample size considerations using dose escalation with overdose control
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+Unifying CRM and EWOC designs for phase I cancer clinical trials
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+Bayesian decision procedures based on logistic regression models for dose-finding studies
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+Adaptive Bayesian compound designs for dose finding studies
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+Convergence properties of sequential Bayesian \(D\)-optimal designs
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+A Semiparametric Sequential Algorithm for Estimation of Dose–Response Curve
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+Sequential Designs for Dose Escalation Studies in Oncology
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+Approximate policy optimization and adaptive control in regression models
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+A new look at evaluating MTD designs in cancer research
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+Retrospective Analysis of Sequential Dose‐Finding Designs
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+A Stochastic Approximation Method
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+Efficient Sequential Designs With Binary Data
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+Sequential Designs in Bioassay
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+Stochastic approximation with virtual observations for dose-finding on discrete levels
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+Dose-Finding with Two Agents in Phase I Oncology Trials
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+Two‐Dimensional Dose Finding in Discrete Dose Space
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+A Latent Contingency Table Approach to Dose Finding for Combinations of Two Agents
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+A Hierarchical Bayesian Design for Phase I Trials of Novel Combinations of Cancer Therapeutic Agents
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+Dose-Finding Based on Multiple Toxicities in a Soft Tissue Sarcoma Trial
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+A Phase I Bayesian Adaptive Design to Simultaneously Optimize Dose and Schedule Assignments Both Between and Within Patients
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+Using Joint Utilities of the Times to Response and Toxicity to Adaptively Optimize Schedule–Dose Regimes
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