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      Bayesian methods in clinical trials with applications to medical devices

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      다국어 초록 (Multilingual Abstract)

      Bayesian statistics can play a key role in the design and analysis of clinical trials and this has been demonstrated for medical device trials. By 1995 Bayesian statistics had been well developed and the revolution in computing powers and Markov chain Monte Carlo development made calculation of posterior distributions within computational reach. The Food and Drug Administration (FDA) initiative of Bayesian statistics in medical device clinical trials, which began almost 20 years ago, is reviewed in detail along with some of the key decisions that were made along the way. Both Bayesian hierarchical modeling using data from previous studies and Bayesian adaptive designs, usually with a non-informative prior, are discussed. The leveraging of prior study data has been accomplished through Bayesian hierarchical modeling. An enormous advantage of Bayesian adaptive designs is achieved when it is accompanied by modeling of the primary endpoint to produce the predictive posterior distribution. Simulations are crucial to providing the operating characteristics of the Bayesian design, especially for a complex adaptive design. The 2010 FDA Bayesian guidance for medical device trials addressed both approaches as well as exchangeability, Type I error, and sample size. Treatment response adaptive randomization using the famous extracorporeal membrane oxygenation example is discussed. An interesting real example of a Bayesian analysis using a failed trial with an interesting subgroup as prior information is presented. The implications of the likelihood principle are considered. A recent exciting area using Bayesian hierarchical modeling has been the pediatric extrapolation using adult data in clinical trials. Historical control information from previous trials is an underused area that lends itself easily to Bayesian methods. The future including recent trends, decision theoretic trials, Bayesian benefit-risk, virtual patients, and the appalling lack of penetration of Bayesian clinical trials in the medical literature are discussed.
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      Bayesian statistics can play a key role in the design and analysis of clinical trials and this has been demonstrated for medical device trials. By 1995 Bayesian statistics had been well developed and the revolution in computing powers and Markov chain...

      Bayesian statistics can play a key role in the design and analysis of clinical trials and this has been demonstrated for medical device trials. By 1995 Bayesian statistics had been well developed and the revolution in computing powers and Markov chain Monte Carlo development made calculation of posterior distributions within computational reach. The Food and Drug Administration (FDA) initiative of Bayesian statistics in medical device clinical trials, which began almost 20 years ago, is reviewed in detail along with some of the key decisions that were made along the way. Both Bayesian hierarchical modeling using data from previous studies and Bayesian adaptive designs, usually with a non-informative prior, are discussed. The leveraging of prior study data has been accomplished through Bayesian hierarchical modeling. An enormous advantage of Bayesian adaptive designs is achieved when it is accompanied by modeling of the primary endpoint to produce the predictive posterior distribution. Simulations are crucial to providing the operating characteristics of the Bayesian design, especially for a complex adaptive design. The 2010 FDA Bayesian guidance for medical device trials addressed both approaches as well as exchangeability, Type I error, and sample size. Treatment response adaptive randomization using the famous extracorporeal membrane oxygenation example is discussed. An interesting real example of a Bayesian analysis using a failed trial with an interesting subgroup as prior information is presented. The implications of the likelihood principle are considered. A recent exciting area using Bayesian hierarchical modeling has been the pediatric extrapolation using adult data in clinical trials. Historical control information from previous trials is an underused area that lends itself easily to Bayesian methods. The future including recent trends, decision theoretic trials, Bayesian benefit-risk, virtual patients, and the appalling lack of penetration of Bayesian clinical trials in the medical literature are discussed.

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      참고문헌 (Reference)

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      60 Simon R, "Bayesian subset analysis : application to studying treatment-by-gender interactions" 21 : 2909-2916, 2002

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      63 Berry DA, "Bayesian statistics and the efficiency and ethics of clinical trials" 19 : 175-187, 2004

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      87 Pedroza C, "Advantages of Bayesian monitoring methods in deciding whether and when to stop a clinical trial : an example of a neonatal cooling trial" 17 : 335-, 2016

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      89 Yang X, "Adaptive design practice at the Center for Devices and Radiological Health(CDRH), January 2007 to May 2013" 50 : 710-717, 2016

      90 Hobbs BP, "Adaptive adjustment of the randomization ratio using historical control data" 10 : 430-440, 2013

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      93 Berry DA, "A case for Bayesianism in clinical trials" 12 : 1377-1393, 1993

      94 Waddingham E, "A Bayesian approach to probabilistic sensitivity analysis in structured benefit-risk assessment" 58 : 28-42, 2015

      95 Grieve AP, "25 years of Bayesian methods in the pharmaceutical industry : a personal, statistical bummel" 6 : 261-281, 2007

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      2022 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2021-12-01 평가 등재후보 탈락 (해외등재 학술지 평가)
      2020-12-01 평가 등재후보로 하락 (해외등재 학술지 평가) KCI등재후보
      2015-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2012-12-21 학술지명변경 한글명 : 한국통계학회 논문집 -> Communications for Statistical Applications and Methods
      외국어명 : Communications of The Korean Statistical Society -> Communications for Statistical Applications and Methods
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      2008-02-05 학술지명변경 외국어명 : The Korean Communications in Statistics -> Communications of The Korean Statistical Society KCI등재
      2007-01-01 평가 등재학술지 유지 (등재유지) KCI등재
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      2016 0.19 0.19 0.17
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