代表 IGNITE ADOPT PGx 研究人员实施一项针对慢性疼痛定制阿片类药物的实用临床试验。

IF 3.1 3区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL Cts-Clinical and Translational Science Pub Date : 2024-08-23 DOI:10.1111/cts.70005
Todd C. Skaar, Rachel A. Myers, Roger B. Fillingim, John T. Callaghan, Emily Cicali, Michael T. Eadon, Erica N. Elwood, Geoffrey S. Ginsburg, Sheryl Lynch, Khoa A. Nguyen, Aniwaa Owusu Obeng, Haesuk Park, Victoria M. Pratt, Marc Rosenman, Azita Sadeghpour, Saskia Shuman, Rajbir Singh, Emma M. Tillman, Simona Volpi, Kristin Wiisanen, Almut G. Winterstein, Carol R. Horowitz, Deepak Voora, Lori Orlando, Hrishikesh Chakraborty, Sara Van Driest, Josh F. Peterson, Larisa A. Cavallari, Julie A. Johnson, Paul R. Dexter, the IGNITE Pragmatic Trials Network
{"title":"代表 IGNITE ADOPT PGx 研究人员实施一项针对慢性疼痛定制阿片类药物的实用临床试验。","authors":"Todd C. Skaar,&nbsp;Rachel A. Myers,&nbsp;Roger B. Fillingim,&nbsp;John T. Callaghan,&nbsp;Emily Cicali,&nbsp;Michael T. Eadon,&nbsp;Erica N. Elwood,&nbsp;Geoffrey S. Ginsburg,&nbsp;Sheryl Lynch,&nbsp;Khoa A. Nguyen,&nbsp;Aniwaa Owusu Obeng,&nbsp;Haesuk Park,&nbsp;Victoria M. Pratt,&nbsp;Marc Rosenman,&nbsp;Azita Sadeghpour,&nbsp;Saskia Shuman,&nbsp;Rajbir Singh,&nbsp;Emma M. Tillman,&nbsp;Simona Volpi,&nbsp;Kristin Wiisanen,&nbsp;Almut G. Winterstein,&nbsp;Carol R. Horowitz,&nbsp;Deepak Voora,&nbsp;Lori Orlando,&nbsp;Hrishikesh Chakraborty,&nbsp;Sara Van Driest,&nbsp;Josh F. Peterson,&nbsp;Larisa A. Cavallari,&nbsp;Julie A. Johnson,&nbsp;Paul R. Dexter,&nbsp;the IGNITE Pragmatic Trials Network","doi":"10.1111/cts.70005","DOIUrl":null,"url":null,"abstract":"<p>Chronic pain is a prevalent condition with enormous economic burden. Opioids such as tramadol, codeine, and hydrocodone are commonly used to treat chronic pain; these drugs are activated to more potent opioid receptor agonists by the hepatic CYP2D6 enzyme. Results from clinical studies and mechanistic understandings suggest that CYP2D6-guided therapy will improve pain control and reduce adverse drug events. However, CYP2D6 is rarely used in clinical practice due in part to the demand for additional clinical trial evidence. Thus, we designed the ADOPT-PGx (A Depression and Opioid Pragmatic Trial in Pharmacogenetics) chronic pain study, a multicenter, pragmatic, randomized controlled clinical trial, to assess the effect of <i>CYP2D6</i> testing on pain management. The study enrolled 1048 participants who are taking or being considered for treatment with CYP2D6-impacted opioids for their chronic pain. Participants were randomized to receive immediate or delayed (by 6 months) genotyping of <i>CYP2D6</i> with clinical decision support (CDS). CDS encouraged the providers to follow the CYP2D6-guided trial recommendations. The primary study outcome is the 3-month absolute change in the composite pain intensity score assessed using Patient-Reported Outcomes Measurement Information System (PROMIS) measures. Follow-up will be completed in July 2024. Herein, we describe the design of this trial along with challenges encountered during enrollment.</p>","PeriodicalId":50610,"journal":{"name":"Cts-Clinical and Translational Science","volume":"17 8","pages":""},"PeriodicalIF":3.1000,"publicationDate":"2024-08-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/cts.70005","citationCount":"0","resultStr":"{\"title\":\"Implementing a pragmatic clinical trial to tailor opioids for chronic pain on behalf of the IGNITE ADOPT PGx investigators\",\"authors\":\"Todd C. Skaar,&nbsp;Rachel A. Myers,&nbsp;Roger B. Fillingim,&nbsp;John T. Callaghan,&nbsp;Emily Cicali,&nbsp;Michael T. Eadon,&nbsp;Erica N. Elwood,&nbsp;Geoffrey S. Ginsburg,&nbsp;Sheryl Lynch,&nbsp;Khoa A. Nguyen,&nbsp;Aniwaa Owusu Obeng,&nbsp;Haesuk Park,&nbsp;Victoria M. Pratt,&nbsp;Marc Rosenman,&nbsp;Azita Sadeghpour,&nbsp;Saskia Shuman,&nbsp;Rajbir Singh,&nbsp;Emma M. Tillman,&nbsp;Simona Volpi,&nbsp;Kristin Wiisanen,&nbsp;Almut G. Winterstein,&nbsp;Carol R. Horowitz,&nbsp;Deepak Voora,&nbsp;Lori Orlando,&nbsp;Hrishikesh Chakraborty,&nbsp;Sara Van Driest,&nbsp;Josh F. Peterson,&nbsp;Larisa A. Cavallari,&nbsp;Julie A. Johnson,&nbsp;Paul R. Dexter,&nbsp;the IGNITE Pragmatic Trials Network\",\"doi\":\"10.1111/cts.70005\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Chronic pain is a prevalent condition with enormous economic burden. Opioids such as tramadol, codeine, and hydrocodone are commonly used to treat chronic pain; these drugs are activated to more potent opioid receptor agonists by the hepatic CYP2D6 enzyme. Results from clinical studies and mechanistic understandings suggest that CYP2D6-guided therapy will improve pain control and reduce adverse drug events. However, CYP2D6 is rarely used in clinical practice due in part to the demand for additional clinical trial evidence. Thus, we designed the ADOPT-PGx (A Depression and Opioid Pragmatic Trial in Pharmacogenetics) chronic pain study, a multicenter, pragmatic, randomized controlled clinical trial, to assess the effect of <i>CYP2D6</i> testing on pain management. The study enrolled 1048 participants who are taking or being considered for treatment with CYP2D6-impacted opioids for their chronic pain. Participants were randomized to receive immediate or delayed (by 6 months) genotyping of <i>CYP2D6</i> with clinical decision support (CDS). CDS encouraged the providers to follow the CYP2D6-guided trial recommendations. The primary study outcome is the 3-month absolute change in the composite pain intensity score assessed using Patient-Reported Outcomes Measurement Information System (PROMIS) measures. Follow-up will be completed in July 2024. Herein, we describe the design of this trial along with challenges encountered during enrollment.</p>\",\"PeriodicalId\":50610,\"journal\":{\"name\":\"Cts-Clinical and Translational Science\",\"volume\":\"17 8\",\"pages\":\"\"},\"PeriodicalIF\":3.1000,\"publicationDate\":\"2024-08-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1111/cts.70005\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cts-Clinical and Translational Science\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/cts.70005\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MEDICINE, RESEARCH & EXPERIMENTAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cts-Clinical and Translational Science","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/cts.70005","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MEDICINE, RESEARCH & EXPERIMENTAL","Score":null,"Total":0}
引用次数: 0

摘要

慢性疼痛是一种普遍存在的疾病,造成了巨大的经济负担。曲马多、可待因和氢可酮等阿片类药物是治疗慢性疼痛的常用药物;这些药物在肝脏 CYP2D6 酶的作用下被激活,成为药效更强的阿片受体激动剂。临床研究结果和机理认识表明,CYP2D6 引导的治疗将改善疼痛控制并减少药物不良反应。然而,CYP2D6 很少用于临床实践,部分原因是需要更多的临床试验证据。因此,我们设计了一项多中心、务实、随机对照临床试验--ADOPT-PGx(药物遗传学中的抑郁和阿片类药物务实试验)慢性疼痛研究,以评估 CYP2D6 检测对疼痛治疗的影响。该研究招募了1048名正在服用或考虑服用受CYP2D6影响的阿片类药物治疗慢性疼痛的参与者。参与者被随机分配到立即或延迟(6 个月)接受临床决策支持(CDS)的 CYP2D6 基因分型。CDS 鼓励医疗服务提供者遵循 CYP2D6 指导的试验建议。主要研究结果是使用患者报告结果测量信息系统 (PROMIS) 评估的综合疼痛强度评分 3 个月的绝对变化。随访将于 2024 年 7 月结束。在此,我们将介绍这项试验的设计以及在注册过程中遇到的挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Implementing a pragmatic clinical trial to tailor opioids for chronic pain on behalf of the IGNITE ADOPT PGx investigators

Chronic pain is a prevalent condition with enormous economic burden. Opioids such as tramadol, codeine, and hydrocodone are commonly used to treat chronic pain; these drugs are activated to more potent opioid receptor agonists by the hepatic CYP2D6 enzyme. Results from clinical studies and mechanistic understandings suggest that CYP2D6-guided therapy will improve pain control and reduce adverse drug events. However, CYP2D6 is rarely used in clinical practice due in part to the demand for additional clinical trial evidence. Thus, we designed the ADOPT-PGx (A Depression and Opioid Pragmatic Trial in Pharmacogenetics) chronic pain study, a multicenter, pragmatic, randomized controlled clinical trial, to assess the effect of CYP2D6 testing on pain management. The study enrolled 1048 participants who are taking or being considered for treatment with CYP2D6-impacted opioids for their chronic pain. Participants were randomized to receive immediate or delayed (by 6 months) genotyping of CYP2D6 with clinical decision support (CDS). CDS encouraged the providers to follow the CYP2D6-guided trial recommendations. The primary study outcome is the 3-month absolute change in the composite pain intensity score assessed using Patient-Reported Outcomes Measurement Information System (PROMIS) measures. Follow-up will be completed in July 2024. Herein, we describe the design of this trial along with challenges encountered during enrollment.

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
Cts-Clinical and Translational Science
Cts-Clinical and Translational Science 医学-医学:研究与实验
CiteScore
6.70
自引率
2.60%
发文量
234
审稿时长
6-12 weeks
期刊介绍: Clinical and Translational Science (CTS), an official journal of the American Society for Clinical Pharmacology and Therapeutics, highlights original translational medicine research that helps bridge laboratory discoveries with the diagnosis and treatment of human disease. Translational medicine is a multi-faceted discipline with a focus on translational therapeutics. In a broad sense, translational medicine bridges across the discovery, development, regulation, and utilization spectrum. Research may appear as Full Articles, Brief Reports, Commentaries, Phase Forwards (clinical trials), Reviews, or Tutorials. CTS also includes invited didactic content that covers the connections between clinical pharmacology and translational medicine. Best-in-class methodologies and best practices are also welcomed as Tutorials. These additional features provide context for research articles and facilitate understanding for a wide array of individuals interested in clinical and translational science. CTS welcomes high quality, scientifically sound, original manuscripts focused on clinical pharmacology and translational science, including animal, in vitro, in silico, and clinical studies supporting the breadth of drug discovery, development, regulation and clinical use of both traditional drugs and innovative modalities.
期刊最新文献
Population pharmacokinetic analysis of quizartinib in patients with newly diagnosed FLT3-internal-tandem-duplication-positive acute myeloid leukemia. Trends of in vitro pharmacological potency and in vivo pharmacokinetics parameters of modern drugs: Can the therapeutic/subtherapeutic dose be estimated from in vitro Ki and pharmacokinetic parameters? Assessment of pharmacokinetics and tolerability following single-dose administration of molnupiravir in participants with hepatic or renal impairment. Deconvoluting zavegepant drug-drug interactions: A phase I study to evaluate the effects of rifampin and itraconazole on zavegepant pharmacokinetics. Safety, tolerability, pharmacokinetics, and pharmacodynamics of the oral allosteric TYK2 inhibitor ESK-001 using a randomized, double-blind, placebo-controlled study design.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1