{"title":"调查数据监测委员会建议对试验成功概率的影响。","authors":"Luca Rondano, Gaëlle Saint-Hilary, Mauro Gasparini, Stefano Vezzoli","doi":"10.1080/10543406.2024.2430308","DOIUrl":null,"url":null,"abstract":"<p><p>Determining the probability of success of a clinical trial using a prior distribution on the treatment effect can significantly enhance decision-making by the sponsor. In a group sequential design, the probability of success calculated at the design stage can be updated to incorporate the information disclosed by the Data Monitoring Committee (DMC), usually consisting in a simple statement that advises to continue or to stop the trial, either for efficacy or futility, following pre-specified rules defined in the protocol. We define the \"probability of success post interim\" as the probability of success conditioned on the assumption that the DMC recommends continuing the trial after an interim analysis. A good assessment of this probability helps mitigate the tendency of the study team to express excessive optimism or unwarranted pessimism regarding the trial's ultimate outcome after the DMC recommendation. We explore the relationship between this \"probability of success post interim\" and the initial probability of success, and we provide an in-depth investigation of how interim boundaries impact these probabilities. This analysis offers valuable insights that can guide the selection of boundaries for both efficacy and futility interim analyses, leading to more informed clinical trial designs.</p>","PeriodicalId":54870,"journal":{"name":"Journal of Biopharmaceutical Statistics","volume":" ","pages":"1-17"},"PeriodicalIF":1.2000,"publicationDate":"2024-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Investigating the impact of data monitoring committee recommendations on the probability of trial success.\",\"authors\":\"Luca Rondano, Gaëlle Saint-Hilary, Mauro Gasparini, Stefano Vezzoli\",\"doi\":\"10.1080/10543406.2024.2430308\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Determining the probability of success of a clinical trial using a prior distribution on the treatment effect can significantly enhance decision-making by the sponsor. In a group sequential design, the probability of success calculated at the design stage can be updated to incorporate the information disclosed by the Data Monitoring Committee (DMC), usually consisting in a simple statement that advises to continue or to stop the trial, either for efficacy or futility, following pre-specified rules defined in the protocol. We define the \\\"probability of success post interim\\\" as the probability of success conditioned on the assumption that the DMC recommends continuing the trial after an interim analysis. A good assessment of this probability helps mitigate the tendency of the study team to express excessive optimism or unwarranted pessimism regarding the trial's ultimate outcome after the DMC recommendation. We explore the relationship between this \\\"probability of success post interim\\\" and the initial probability of success, and we provide an in-depth investigation of how interim boundaries impact these probabilities. This analysis offers valuable insights that can guide the selection of boundaries for both efficacy and futility interim analyses, leading to more informed clinical trial designs.</p>\",\"PeriodicalId\":54870,\"journal\":{\"name\":\"Journal of Biopharmaceutical Statistics\",\"volume\":\" \",\"pages\":\"1-17\"},\"PeriodicalIF\":1.2000,\"publicationDate\":\"2024-12-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Biopharmaceutical Statistics\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1080/10543406.2024.2430308\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"PHARMACOLOGY & PHARMACY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Biopharmaceutical Statistics","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/10543406.2024.2430308","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
Investigating the impact of data monitoring committee recommendations on the probability of trial success.
Determining the probability of success of a clinical trial using a prior distribution on the treatment effect can significantly enhance decision-making by the sponsor. In a group sequential design, the probability of success calculated at the design stage can be updated to incorporate the information disclosed by the Data Monitoring Committee (DMC), usually consisting in a simple statement that advises to continue or to stop the trial, either for efficacy or futility, following pre-specified rules defined in the protocol. We define the "probability of success post interim" as the probability of success conditioned on the assumption that the DMC recommends continuing the trial after an interim analysis. A good assessment of this probability helps mitigate the tendency of the study team to express excessive optimism or unwarranted pessimism regarding the trial's ultimate outcome after the DMC recommendation. We explore the relationship between this "probability of success post interim" and the initial probability of success, and we provide an in-depth investigation of how interim boundaries impact these probabilities. This analysis offers valuable insights that can guide the selection of boundaries for both efficacy and futility interim analyses, leading to more informed clinical trial designs.
期刊介绍:
The Journal of Biopharmaceutical Statistics, a rapid publication journal, discusses quality applications of statistics in biopharmaceutical research and development. Now publishing six times per year, it includes expositions of statistical methodology with immediate applicability to biopharmaceutical research in the form of full-length and short manuscripts, review articles, selected/invited conference papers, short articles, and letters to the editor. Addressing timely and provocative topics important to the biostatistical profession, the journal covers:
Drug, device, and biological research and development;
Drug screening and drug design;
Assessment of pharmacological activity;
Pharmaceutical formulation and scale-up;
Preclinical safety assessment;
Bioavailability, bioequivalence, and pharmacokinetics;
Phase, I, II, and III clinical development including complex innovative designs;
Premarket approval assessment of clinical safety;
Postmarketing surveillance;
Big data and artificial intelligence and applications.