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점증적 용량 설계 (지속적 재평가 방법)×베이즈 추론×
분야실험설계통계학
계열Process / pipelineBayesian methods
기원 연도19901763
창시자John O'Quigley, Margaret Pepe & Lloyd FisherThomas Bayes; Pierre-Simon Laplace
유형Adaptive Bayesian dose-finding designProbabilistic inference paradigm
원전O'Quigley, J., Pepe, M., & Fisher, L. (1990). Continual reassessment method: a practical design for phase 1 clinical trials in cancer. Biometrics, 46(1), 33–48. DOI ↗Bayes, T. (1763). An essay towards solving a problem in the doctrine of chances. Philosophical Transactions of the Royal Society of London, 53, 370–418. link ↗
별칭Continual Reassessment Method, CRM Design, Phase I Dose-Finding Design, Doz Artırma TasarımıBayes inference, Bayesian statistics, Bayesian updating, posterior inference
관련23
요약Dose-Escalation Design, formalized as the Continual Reassessment Method (CRM), is a Bayesian adaptive algorithm for identifying the Maximum Tolerated Dose (MTD) in Phase I clinical trials. Introduced by John O'Quigley, Margaret Pepe, and Lloyd Fisher in 1990, CRM treats dose-toxicity response as a parametric curve, updates a prior probability model after each patient's outcome, and assigns subsequent patients to the dose currently estimated closest to a pre-specified target toxicity probability.Bayesian inference is a statistical paradigm in which probability represents degrees of belief rather than long-run frequencies. It encodes prior knowledge about parameters in a prior distribution, combines that prior with the likelihood of observed data via Bayes' theorem, and produces a posterior distribution that quantifies updated uncertainty. The foundational theorem was published posthumously by Thomas Bayes in 1763 and subsequently systematized by Pierre-Simon Laplace in his 1812 Théorie analytique des probabilités.
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ScholarGate방법 비교: Dose-Escalation Design · Bayesian Inference. 2026-06-17에 다음에서 검색함: https://scholargate.app/ko/compare