针对罕见病的负责任临床n-of-1策略。

IF 6.5 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Victoria M. Defelippe , Ghislaine J.M.W. van Thiel , Willem M. Otte , Roger E.G. Schutgens , Bas Stunnenberg , Helen J. Cross , Finbar O'Callaghan , Valentina De Giorgis , Floor E. Jansen , Emilio Perucca , Eva H. Brilstra , Kees P.J. Braun
{"title":"针对罕见病的负责任临床n-of-1策略。","authors":"Victoria M. Defelippe ,&nbsp;Ghislaine J.M.W. van Thiel ,&nbsp;Willem M. Otte ,&nbsp;Roger E.G. Schutgens ,&nbsp;Bas Stunnenberg ,&nbsp;Helen J. Cross ,&nbsp;Finbar O'Callaghan ,&nbsp;Valentina De Giorgis ,&nbsp;Floor E. Jansen ,&nbsp;Emilio Perucca ,&nbsp;Eva H. Brilstra ,&nbsp;Kees P.J. Braun","doi":"10.1016/j.drudis.2023.103688","DOIUrl":null,"url":null,"abstract":"<div><p><em>N</em>-of-1 strategies can provide high-quality evidence of treatment efficacy at the individual level and optimize evidence-based selection of off-label treatments for patients with rare diseases. Given their design characteristics, <em>n</em>-of-1 strategies are considered to lay at the intersection between medical research and clinical care. Therefore, whether <em>n</em>-of-1 strategies should be governed by research or care regulations remains a debated issue. Here, we delineate differences between medical research and optimized clinical care, and distinguish the regulations which apply to either. We also set standards for responsible optimized clinical <em>n</em>-of-1 strategies with (off-label) treatments for rare diseases. Implementing clinical <em>n</em>-of-1 strategies as defined here could aid in optimized treatment selection for such diseases.</p></div>","PeriodicalId":301,"journal":{"name":"Drug Discovery Today","volume":"28 10","pages":"Article 103688"},"PeriodicalIF":6.5000,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1359644623002040/pdfft?md5=0ec274864e82ec2cead4c8049fc7384a&pid=1-s2.0-S1359644623002040-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Toward responsible clinical n-of-1 strategies for rare diseases\",\"authors\":\"Victoria M. Defelippe ,&nbsp;Ghislaine J.M.W. van Thiel ,&nbsp;Willem M. Otte ,&nbsp;Roger E.G. Schutgens ,&nbsp;Bas Stunnenberg ,&nbsp;Helen J. Cross ,&nbsp;Finbar O'Callaghan ,&nbsp;Valentina De Giorgis ,&nbsp;Floor E. Jansen ,&nbsp;Emilio Perucca ,&nbsp;Eva H. Brilstra ,&nbsp;Kees P.J. Braun\",\"doi\":\"10.1016/j.drudis.2023.103688\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><em>N</em>-of-1 strategies can provide high-quality evidence of treatment efficacy at the individual level and optimize evidence-based selection of off-label treatments for patients with rare diseases. Given their design characteristics, <em>n</em>-of-1 strategies are considered to lay at the intersection between medical research and clinical care. Therefore, whether <em>n</em>-of-1 strategies should be governed by research or care regulations remains a debated issue. Here, we delineate differences between medical research and optimized clinical care, and distinguish the regulations which apply to either. We also set standards for responsible optimized clinical <em>n</em>-of-1 strategies with (off-label) treatments for rare diseases. Implementing clinical <em>n</em>-of-1 strategies as defined here could aid in optimized treatment selection for such diseases.</p></div>\",\"PeriodicalId\":301,\"journal\":{\"name\":\"Drug Discovery Today\",\"volume\":\"28 10\",\"pages\":\"Article 103688\"},\"PeriodicalIF\":6.5000,\"publicationDate\":\"2023-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S1359644623002040/pdfft?md5=0ec274864e82ec2cead4c8049fc7384a&pid=1-s2.0-S1359644623002040-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Drug Discovery Today\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1359644623002040\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PHARMACOLOGY & PHARMACY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Drug Discovery Today","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1359644623002040","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0

摘要

N选1策略可以在个人层面提供高质量的治疗效果证据,并优化罕见病患者的循证选择。鉴于其设计特点,n-of-1策略被认为是医学研究和临床护理之间的交叉点。因此,n-of-1策略是否应该由研究或护理法规来管理仍然是一个有争议的问题。在这里,我们描述了医学研究和优化临床护理之间的差异,并区分了适用于两者的法规。我们还为负责任的优化临床n-of-1策略制定了标准,用于罕见病的(标签外)治疗。实施本文定义的临床n-of-1策略可以帮助优化此类疾病的治疗选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Toward responsible clinical n-of-1 strategies for rare diseases

N-of-1 strategies can provide high-quality evidence of treatment efficacy at the individual level and optimize evidence-based selection of off-label treatments for patients with rare diseases. Given their design characteristics, n-of-1 strategies are considered to lay at the intersection between medical research and clinical care. Therefore, whether n-of-1 strategies should be governed by research or care regulations remains a debated issue. Here, we delineate differences between medical research and optimized clinical care, and distinguish the regulations which apply to either. We also set standards for responsible optimized clinical n-of-1 strategies with (off-label) treatments for rare diseases. Implementing clinical n-of-1 strategies as defined here could aid in optimized treatment selection for such diseases.

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
Drug Discovery Today
Drug Discovery Today 医学-药学
CiteScore
14.80
自引率
2.70%
发文量
293
审稿时长
6 months
期刊介绍: Drug Discovery Today delivers informed and highly current reviews for the discovery community. The magazine addresses not only the rapid scientific developments in drug discovery associated technologies but also the management, commercial and regulatory issues that increasingly play a part in how R&D is planned, structured and executed. Features include comment by international experts, news and analysis of important developments, reviews of key scientific and strategic issues, overviews of recent progress in specific therapeutic areas and conference reports.
×
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