ABC-12:在durvalumab (MEDI4736)联合顺铂/吉西他滨的一线研究中探索晚期胆道癌患者的微生物组。

IF 2.6 4区 医学 Q2 ONCOLOGY
Future oncology Pub Date : 2025-09-01 Epub Date: 2025-07-29 DOI:10.1080/14796694.2025.2539018
Eleni Vrana, Hayley Timmins, Ashley Osborne, Rebecca Cox, Harpreet Wasan, Yuk Ting Ma, Arvind Arora, Olusola Faluyi, Roopinder Gillmore, Pippa Corrie, Paul Miller, Seema Arif, Joanna Canham, Charlotte Martin, Muhammad Riaz, Tongtong Shi, Melissa Frizziero, Victoria Foy, Richard A Hubner, Helen Morement, John Bridgewater, Richard Adams, Juan W Valle, Mairéad G McNamara
{"title":"ABC-12:在durvalumab (MEDI4736)联合顺铂/吉西他滨的一线研究中探索晚期胆道癌患者的微生物组。","authors":"Eleni Vrana, Hayley Timmins, Ashley Osborne, Rebecca Cox, Harpreet Wasan, Yuk Ting Ma, Arvind Arora, Olusola Faluyi, Roopinder Gillmore, Pippa Corrie, Paul Miller, Seema Arif, Joanna Canham, Charlotte Martin, Muhammad Riaz, Tongtong Shi, Melissa Frizziero, Victoria Foy, Richard A Hubner, Helen Morement, John Bridgewater, Richard Adams, Juan W Valle, Mairéad G McNamara","doi":"10.1080/14796694.2025.2539018","DOIUrl":null,"url":null,"abstract":"<p><p>Until recently, cisplatin/gemcitabine was standard of care for the first-line treatment of patients with advanced biliary tract cancer (BTC). The addition of durvalumab, an immune checkpoint inhibitor, to the combination of cisplatin/gemcitabine has demonstrated an overall survival (OS) benefit and is now a standard of care first-line treatment option. BTCs exhibit immunogenic features may develop through an accumulation of genetic and epigenetic alterations, and can be influenced by microbial exposure. Microbiota can influence inflammation and immunity, and its disruption may impair tumor response to immunotherapy and chemotherapy. Here, the rationale and design of the multi-center, single-arm ABC-12 trial (ISRCTN11210442) is described, which investigates the role of the microbiome in patients with advanced BTC in a first-line study of durvalumab (MEDI4736) in combination with cisplatin/gemcitabine. The primary objective is to determine the difference in baseline alpha diversity between \"responders\" (partial or complete response) and \"non-responders\" at 18 weeks (RECIST 1.1) in patients treated with cisplatin/gemcitabine/durvalumab. Secondary objectives include investigating the association between microbiome parameters and objective response rate, tumor control (partial, complete response, and stable disease), progression-free and OS, and investigating the interaction between treatment effect and microbiome parameters on clinical outcomes.</p>","PeriodicalId":12672,"journal":{"name":"Future oncology","volume":" ","pages":"2713-2721"},"PeriodicalIF":2.6000,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12407636/pdf/","citationCount":"0","resultStr":"{\"title\":\"ABC-12: exploring the microbiome in patients with advanced biliary tract cancer in a first-line study of durvalumab (MEDI4736) in combination with cisplatin/gemcitabine.\",\"authors\":\"Eleni Vrana, Hayley Timmins, Ashley Osborne, Rebecca Cox, Harpreet Wasan, Yuk Ting Ma, Arvind Arora, Olusola Faluyi, Roopinder Gillmore, Pippa Corrie, Paul Miller, Seema Arif, Joanna Canham, Charlotte Martin, Muhammad Riaz, Tongtong Shi, Melissa Frizziero, Victoria Foy, Richard A Hubner, Helen Morement, John Bridgewater, Richard Adams, Juan W Valle, Mairéad G McNamara\",\"doi\":\"10.1080/14796694.2025.2539018\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Until recently, cisplatin/gemcitabine was standard of care for the first-line treatment of patients with advanced biliary tract cancer (BTC). The addition of durvalumab, an immune checkpoint inhibitor, to the combination of cisplatin/gemcitabine has demonstrated an overall survival (OS) benefit and is now a standard of care first-line treatment option. BTCs exhibit immunogenic features may develop through an accumulation of genetic and epigenetic alterations, and can be influenced by microbial exposure. Microbiota can influence inflammation and immunity, and its disruption may impair tumor response to immunotherapy and chemotherapy. Here, the rationale and design of the multi-center, single-arm ABC-12 trial (ISRCTN11210442) is described, which investigates the role of the microbiome in patients with advanced BTC in a first-line study of durvalumab (MEDI4736) in combination with cisplatin/gemcitabine. The primary objective is to determine the difference in baseline alpha diversity between \\\"responders\\\" (partial or complete response) and \\\"non-responders\\\" at 18 weeks (RECIST 1.1) in patients treated with cisplatin/gemcitabine/durvalumab. Secondary objectives include investigating the association between microbiome parameters and objective response rate, tumor control (partial, complete response, and stable disease), progression-free and OS, and investigating the interaction between treatment effect and microbiome parameters on clinical outcomes.</p>\",\"PeriodicalId\":12672,\"journal\":{\"name\":\"Future oncology\",\"volume\":\" \",\"pages\":\"2713-2721\"},\"PeriodicalIF\":2.6000,\"publicationDate\":\"2025-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12407636/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Future oncology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1080/14796694.2025.2539018\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/7/29 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"ONCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Future oncology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/14796694.2025.2539018","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/7/29 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

直到最近,顺铂/吉西他滨一直是晚期胆道癌(BTC)患者一线治疗的标准治疗方案。在顺铂/吉西他滨联合治疗中加入免疫检查点抑制剂durvalumab已经证明了总生存期(OS)的益处,并且现在是一线治疗的标准选择。btc表现出免疫原性特征,可能通过遗传和表观遗传改变的积累而发展,并可能受到微生物暴露的影响。微生物群可以影响炎症和免疫,其破坏可能会损害肿瘤对免疫治疗和化疗的反应。本文描述了多中心、单组ABC-12试验(ISRCTN11210442)的基本原理和设计,该试验在durvalumab (MEDI4736)联合顺铂/吉西他滨的一线研究中调查了微生物组在晚期BTC患者中的作用。主要目的是确定在顺铂/吉西他滨/杜伐单抗治疗患者18周时“应答者”(部分或完全应答)和“无应答者”(RECIST 1.1)之间基线α多样性的差异。次要目标包括研究微生物组参数与客观缓解率、肿瘤控制(部分缓解、完全缓解和疾病稳定)、无进展和OS之间的关系,以及研究治疗效果和微生物组参数对临床结果的相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
ABC-12: exploring the microbiome in patients with advanced biliary tract cancer in a first-line study of durvalumab (MEDI4736) in combination with cisplatin/gemcitabine.

Until recently, cisplatin/gemcitabine was standard of care for the first-line treatment of patients with advanced biliary tract cancer (BTC). The addition of durvalumab, an immune checkpoint inhibitor, to the combination of cisplatin/gemcitabine has demonstrated an overall survival (OS) benefit and is now a standard of care first-line treatment option. BTCs exhibit immunogenic features may develop through an accumulation of genetic and epigenetic alterations, and can be influenced by microbial exposure. Microbiota can influence inflammation and immunity, and its disruption may impair tumor response to immunotherapy and chemotherapy. Here, the rationale and design of the multi-center, single-arm ABC-12 trial (ISRCTN11210442) is described, which investigates the role of the microbiome in patients with advanced BTC in a first-line study of durvalumab (MEDI4736) in combination with cisplatin/gemcitabine. The primary objective is to determine the difference in baseline alpha diversity between "responders" (partial or complete response) and "non-responders" at 18 weeks (RECIST 1.1) in patients treated with cisplatin/gemcitabine/durvalumab. Secondary objectives include investigating the association between microbiome parameters and objective response rate, tumor control (partial, complete response, and stable disease), progression-free and OS, and investigating the interaction between treatment effect and microbiome parameters on clinical outcomes.

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
Future oncology
Future oncology ONCOLOGY-
CiteScore
5.40
自引率
3.00%
发文量
335
审稿时长
4-8 weeks
期刊介绍: Future Oncology (ISSN 1479-6694) provides a forum for a new era of cancer care. The journal focuses on the most important advances and highlights their relevance in the clinical setting. Furthermore, Future Oncology delivers essential information in concise, at-a-glance article formats - vital in delivering information to an increasingly time-constrained community. The journal takes a forward-looking stance toward the scientific and clinical issues, together with the economic and policy issues that confront us in this new era of cancer care. The journal includes literature awareness such as the latest developments in radiotherapy and immunotherapy, concise commentary and analysis, and full review articles all of which provide key findings, translational to the clinical setting.
×
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:604180095
Book学术官方微信