• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Bayesian multiregional clinical trials using model averaging.贝叶斯多区域临床试验中的模型平均法。
Biostatistics. 2023 Apr 14;24(2):262-276. doi: 10.1093/biostatistics/kxab027.
2
Bayesian design of multi-regional clinical trials with time-to-event endpoints.贝叶斯设计的多区域临床试验与时间事件终点。
Biometrics. 2023 Dec;79(4):3586-3598. doi: 10.1111/biom.13820. Epub 2023 Jan 12.
3
Bayesian joint models for multi-regional clinical trials.贝叶斯联合模型在多区域临床试验中的应用。
Biostatistics. 2024 Jul 1;25(3):852-866. doi: 10.1093/biostatistics/kxad023.
4
Cautionary note on regional consistency evaluation in multiregional clinical trials with binary outcomes.关于二分类结局的多区域临床试验中区域一致性评价的警示。
Pharm Stat. 2024 May-Jun;23(3):385-398. doi: 10.1002/pst.2358. Epub 2023 Dec 20.
5
Sample size allocation in multiregional equivalence studies.多区域等效性研究中的样本量分配
Pharm Stat. 2018 Sep;17(5):570-577. doi: 10.1002/pst.1871. Epub 2018 Jun 17.
6
Statistical design of noninferiority multiple region clinical trials to assess global and consistent treatment effects.用于评估全球一致治疗效果的非劣效性多区域临床试验的统计设计。
J Biopharm Stat. 2017;27(6):933-944. doi: 10.1080/10543406.2017.1293075. Epub 2017 Mar 15.
7
An empirical Bayes approach to evaluation of results for a specific region in multiregional clinical trials.一种用于评估多区域临床试验中特定区域结果的经验贝叶斯方法。
Pharm Stat. 2013 Mar-Apr;12(2):59-64. doi: 10.1002/pst.1553. Epub 2013 Jan 14.
8
Points to Consider for Implementation of the ICH E17 Guideline: Learning from Past Multiregional Clinical Trials in Japan.ICH E17 实施指南要点:从日本以往多区域临床试验中汲取经验。
Clin Pharmacol Ther. 2021 Jun;109(6):1555-1563. doi: 10.1002/cpt.2121. Epub 2020 Dec 16.
9
Assessing the consistency of the treatment effect under the discrete random effects model in multiregional clinical trials.评估多区域临床试验中离散随机效应模型下治疗效果的一致性。
Stat Med. 2016 Jun 30;35(14):2301-14. doi: 10.1002/sim.6869. Epub 2016 Feb 2.
10
Sample size estimation of multiregional clinical trials with heterogeneous variability across regions.各区域间变异性存在差异的多区域临床试验的样本量估计
J Biopharm Stat. 2014;24(2):254-71. doi: 10.1080/10543406.2013.859150.

引用本文的文献

1
Testing for Similarity of Dose Response in Multiregional Clinical Trials.多区域临床试验中剂量反应相似性的检验
Stat Med. 2025 Sep;44(20-22):e70255. doi: 10.1002/sim.70255.
2
Bayesian joint models for multi-regional clinical trials.贝叶斯联合模型在多区域临床试验中的应用。
Biostatistics. 2024 Jul 1;25(3):852-866. doi: 10.1093/biostatistics/kxad023.

本文引用的文献

1
Bayesian adaptive basket trial design using model averaging.基于模型平均的贝叶斯自适应篮子试验设计。
Biostatistics. 2021 Jan 28;22(1):19-34. doi: 10.1093/biostatistics/kxz014.
2
Strategic inclusion of regions in multiregional clinical trials.多区域临床试验中的区域战略性纳入。
Clin Trials. 2019 Feb;16(1):98-105. doi: 10.1177/1740774518813573. Epub 2018 Nov 16.
3
Use of interval estimations in design and evaluation of multiregional clinical trials with continuous outcomes.使用区间估计设计和评估具有连续结局的多区域临床试验。
Stat Methods Med Res. 2019 Jul;28(7):2179-2195. doi: 10.1177/0962280217751277. Epub 2018 Jan 22.
4
Unified additional requirement in consideration of regional approval for multiregional clinical trials.考虑多区域临床试验的区域批准的统一附加要求。
J Biopharm Stat. 2017;27(6):903-917. doi: 10.1080/10543406.2017.1289942. Epub 2017 Mar 13.
5
A randomised, phase III trial of once-daily fluticasone furoate/vilanterol 100/25 μg versus once-daily vilanterol 25 μg to evaluate the contribution on lung function of fluticasone furoate in the combination in patients with COPD.一项随机、III期试验,比较每日一次糠酸氟替卡松/维兰特罗100/25μg与每日一次维兰特罗25μg,以评估糠酸氟替卡松在慢性阻塞性肺疾病患者联合用药中对肺功能的作用。
Respir Med. 2017 Feb;123:8-17. doi: 10.1016/j.rmed.2016.12.001. Epub 2016 Dec 2.
6
Liraglutide and Cardiovascular Outcomes in Type 2 Diabetes.利拉鲁肽与2型糖尿病患者的心血管结局
N Engl J Med. 2016 Jul 28;375(4):311-22. doi: 10.1056/NEJMoa1603827. Epub 2016 Jun 13.
7
Assessing the consistency of the treatment effect under the discrete random effects model in multiregional clinical trials.评估多区域临床试验中离散随机效应模型下治疗效果的一致性。
Stat Med. 2016 Jun 30;35(14):2301-14. doi: 10.1002/sim.6869. Epub 2016 Feb 2.
8
Designing multiregional trials under the discrete random effects model.在离散随机效应模型下设计多区域试验。
J Biopharm Stat. 2014;24(2):415-28. doi: 10.1080/10543406.2013.860155.
9
Sample size estimation of multiregional clinical trials with heterogeneous variability across regions.各区域间变异性存在差异的多区域临床试验的样本量估计
J Biopharm Stat. 2014;24(2):254-71. doi: 10.1080/10543406.2013.859150.
10
Multi-regional clinical trial design and consistency assessment of treatment effects.多地区临床试验设计与治疗效果的一致性评估。
Stat Med. 2014 Jun 15;33(13):2191-205. doi: 10.1002/sim.6108. Epub 2014 Feb 11.

贝叶斯多区域临床试验中的模型平均法。

Bayesian multiregional clinical trials using model averaging.

机构信息

Department of Biostatistics, University of North Carolina, McGavran-Greenberg Hall, CB #7420, Chapel Hill, NC 27599, USA.

出版信息

Biostatistics. 2023 Apr 14;24(2):262-276. doi: 10.1093/biostatistics/kxab027.

DOI:10.1093/biostatistics/kxab027
PMID:34296263
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10102881/
Abstract

Multiregional clinical trials (MRCTs) provide the benefit of more rapidly introducing drugs to the global market; however, small regional sample sizes can lead to poor estimation quality of region-specific effects when using current statistical methods. With the publication of the International Conference for Harmonisation E17 guideline in 2017, the MRCT design is recognized as a viable strategy that can be accepted by regional regulatory authorities, necessitating new statistical methods that improve the quality of region-specific inference. In this article, we develop a novel methodology for estimating region-specific and global treatment effects for MRCTs using Bayesian model averaging. This approach can be used for trials that compare two treatment groups with respect to a continuous outcome, and it allows for the incorporation of patient characteristics through the inclusion of covariates. We propose an approach that uses posterior model probabilities to quantify evidence in favor of consistency of treatment effects across all regions, and this metric can be used by regulatory authorities for drug approval. We show through simulations that the proposed modeling approach results in lower MSE than a fixed-effects linear regression model and better control of type I error rates than a Bayesian hierarchical model.

摘要

多地区临床试验(MRCTs)提供了将药物更快推向全球市场的好处;然而,当使用当前的统计方法时,小区域样本量可能导致对特定区域效果的估计质量较差。随着 2017 年国际协调会议 E17 指南的发布,MRCT 设计被认为是一种可行的策略,可以被地区监管机构接受,这需要新的统计方法来提高特定区域推断的质量。在本文中,我们开发了一种使用贝叶斯模型平均法估计 MRCT 中特定区域和全球治疗效果的新方法。这种方法可用于比较两种治疗组在连续结果方面的试验,并且可以通过包含协变量来纳入患者特征。我们提出了一种使用后验模型概率来量化所有地区治疗效果一致性证据的方法,该方法可由监管机构用于药物批准。我们通过模拟表明,所提出的建模方法导致均方误差(MSE)低于固定效应线性回归模型,并且比贝叶斯层次模型更好地控制了 I 型错误率。