调查数据监测委员会建议对试验成功概率的影响。

IF 1.2 4区 医学 Q4 PHARMACOLOGY & PHARMACY
Luca Rondano, Gaëlle Saint-Hilary, Mauro Gasparini, Stefano Vezzoli
{"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}
引用次数: 0

摘要

利用治疗效果的先验分布来确定临床试验成功的概率,可以显著提高申办者的决策能力。在组序设计中,在设计阶段计算的成功概率可以更新,以纳入数据监测委员会(DMC)披露的信息,通常包括一个简单的声明,建议继续或停止试验,无论是有效还是无效,遵循协议中预定义的规则。我们将“中期后的成功概率”定义为成功的概率,其条件是DMC在中期分析后建议继续进行试验。对这种可能性的良好评估有助于减轻研究团队在DMC推荐后对试验最终结果表达过度乐观或毫无根据的悲观的倾向。我们探讨了这种“过渡后成功概率”与初始成功概率之间的关系,并深入研究了过渡边界如何影响这些概率。该分析提供了有价值的见解,可以指导有效性和无效性中期分析的边界选择,从而导致更明智的临床试验设计。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Journal of Biopharmaceutical Statistics
Journal of Biopharmaceutical Statistics 医学-统计学与概率论
CiteScore
2.50
自引率
18.20%
发文量
71
审稿时长
6-12 weeks
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.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信