Neoadjuvant chemoradiotherapy followed by active surveillance versus standard surgery for oesophageal cancer (SANO trial): a multicentre, stepped-wedge, cluster-randomised, non-inferiority, phase 3 trial

Berend J van der Wilk, Ben M Eyck, Bas P L Wijnhoven, Sjoerd M Lagarde, Camiel Rosman, Bo J Noordman, Maria J Valkema, Tanya M Bisseling, Peter-Paul L O Coene, Marc J van Det, Jan Willem T Dekker, Jolanda M van Dieren, Michail Doukas, Stijn van Esser, W Edward Fiets, Henk H Hartgrink, Joos Heisterkamp, I Lisanne Holster, Bastiaan Klarenbeek, David van Klaveren, Walther Jansen
{"title":"Neoadjuvant chemoradiotherapy followed by active surveillance versus standard surgery for oesophageal cancer (SANO trial): a multicentre, stepped-wedge, cluster-randomised, non-inferiority, phase 3 trial","authors":"Berend J van der Wilk, Ben M Eyck, Bas P L Wijnhoven, Sjoerd M Lagarde, Camiel Rosman, Bo J Noordman, Maria J Valkema, Tanya M Bisseling, Peter-Paul L O Coene, Marc J van Det, Jan Willem T Dekker, Jolanda M van Dieren, Michail Doukas, Stijn van Esser, W Edward Fiets, Henk H Hartgrink, Joos Heisterkamp, I Lisanne Holster, Bastiaan Klarenbeek, David van Klaveren, Walther Jansen","doi":"10.1016/s1470-2045(25)00027-0","DOIUrl":null,"url":null,"abstract":"<h3>Background</h3>A substantial proportion of individuals with oesophageal cancer have a pathological complete response after neoadjuvant chemoradiotherapy and oesophagectomy. We aimed to investigate whether active surveillance could be an alternative for individuals with a clinical complete response after neoadjuvant chemoradiotherapy.<h3>Methods</h3>We performed a multicentre, stepped-wedge, cluster-randomised, non-inferiority, phase 3 trial in 12 Dutch hospitals. Individuals with locally advanced oesophageal cancer and a clinical complete response after neoadjuvant chemoradiotherapy (ie, no tumour detected with endoscopic biopsies, ultrasound, and PET-CT) underwent active surveillance or standard surgery (ie, oesophagectomy within 2 weeks after reaching clinical complete response). There were no inclusion restrictions regarding comorbidities or performance status, but participants had carcinoma, were age 18 years or older, and were treated with curative intent. Randomisation of hospitals was performed using computer-generated sequences without stratification methods, after an initial phase of all hospitals performing standard surgery. The primary endpoint was overall survival, analysed according to a modified intention-to-treat principle (allowing crossover at time of clinical complete response) and an intention-to-treat principle. Non-inferiority was defined as 2-year survival rate for active surveillance of 15% or less below that for standard surgery. The trial was registered within the Netherlands Trial Register, NTR-6803, and the inclusion phase has been completed.<h3>Findings</h3>Between Nov 8, 2017, and Jan 17, 2021, 1115 individuals were screened, of whom 309 were included. 198 underwent active surveillance and 111 underwent standard surgery. 242 (78%) participants were male and 67 (22%) were female. Median follow-up was 38 months (IQR 32–48). 2-year overall survival for active surveillance (74% [95% CI 69–78]) was non-inferior to standard surgery (71% [62–78]) after modified intention-to-treat analysis (one-sided 95% boundary: 7% lower). It remained non-inferior in the intention-to-treat analysis (75% [68–80] <em>vs</em> 70% [63–77], one-sided 95% boundary: 6% lower). There were no significant differences in overall survival according to modified intention-to-treat analysis (hazard ratio 1·14, two-sided 95% CI 0·74–1·78) or intention-to-treat analysis (0·83, 0·53–1·31). The frequency of postoperative complications and postoperative mortality after standard surgery or postponed surgery after active surveillance was similar between groups.<h3>Interpretation</h3>Overall survival after active surveillance for oesophageal cancer was non-inferior compared with standard surgery after 2 years. For the long-term efficacy of active surveillance, extended follow-up is required. The results of the present trial could be used for patient counselling and shared decision making.<h3>Funding</h3>Dutch Cancer Society (KWF) and Netherlands Organisation for Health Research and Development (ZonMw).","PeriodicalId":22865,"journal":{"name":"The Lancet Oncology","volume":"33 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-03-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Lancet Oncology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/s1470-2045(25)00027-0","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Background

A substantial proportion of individuals with oesophageal cancer have a pathological complete response after neoadjuvant chemoradiotherapy and oesophagectomy. We aimed to investigate whether active surveillance could be an alternative for individuals with a clinical complete response after neoadjuvant chemoradiotherapy.

Methods

We performed a multicentre, stepped-wedge, cluster-randomised, non-inferiority, phase 3 trial in 12 Dutch hospitals. Individuals with locally advanced oesophageal cancer and a clinical complete response after neoadjuvant chemoradiotherapy (ie, no tumour detected with endoscopic biopsies, ultrasound, and PET-CT) underwent active surveillance or standard surgery (ie, oesophagectomy within 2 weeks after reaching clinical complete response). There were no inclusion restrictions regarding comorbidities or performance status, but participants had carcinoma, were age 18 years or older, and were treated with curative intent. Randomisation of hospitals was performed using computer-generated sequences without stratification methods, after an initial phase of all hospitals performing standard surgery. The primary endpoint was overall survival, analysed according to a modified intention-to-treat principle (allowing crossover at time of clinical complete response) and an intention-to-treat principle. Non-inferiority was defined as 2-year survival rate for active surveillance of 15% or less below that for standard surgery. The trial was registered within the Netherlands Trial Register, NTR-6803, and the inclusion phase has been completed.

Findings

Between Nov 8, 2017, and Jan 17, 2021, 1115 individuals were screened, of whom 309 were included. 198 underwent active surveillance and 111 underwent standard surgery. 242 (78%) participants were male and 67 (22%) were female. Median follow-up was 38 months (IQR 32–48). 2-year overall survival for active surveillance (74% [95% CI 69–78]) was non-inferior to standard surgery (71% [62–78]) after modified intention-to-treat analysis (one-sided 95% boundary: 7% lower). It remained non-inferior in the intention-to-treat analysis (75% [68–80] vs 70% [63–77], one-sided 95% boundary: 6% lower). There were no significant differences in overall survival according to modified intention-to-treat analysis (hazard ratio 1·14, two-sided 95% CI 0·74–1·78) or intention-to-treat analysis (0·83, 0·53–1·31). The frequency of postoperative complications and postoperative mortality after standard surgery or postponed surgery after active surveillance was similar between groups.

Interpretation

Overall survival after active surveillance for oesophageal cancer was non-inferior compared with standard surgery after 2 years. For the long-term efficacy of active surveillance, extended follow-up is required. The results of the present trial could be used for patient counselling and shared decision making.

Funding

Dutch Cancer Society (KWF) and Netherlands Organisation for Health Research and Development (ZonMw).
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
新辅助放化疗后主动监测与食管癌标准手术(SANO试验):一项多中心、楔形踏步、集群随机、非劣效性的3期试验
背景:相当一部分食管癌患者在新辅助放化疗和食管切除术后病理完全缓解。我们的目的是研究主动监测是否可以作为新辅助放化疗后临床完全缓解的个体的替代方案。方法:我们在荷兰12家医院进行了一项多中心、楔形、集群随机、非劣效性的3期试验。局部晚期食管癌患者在新辅助放化疗后临床完全缓解(即内镜活检、超声和PET-CT未发现肿瘤),接受主动监测或标准手术(即在达到临床完全缓解后2周内进行食管切除术)。没有关于合并症或表现状态的纳入限制,但参与者患有癌症,年龄在18岁或以上,并且以治愈为目的进行治疗。在所有医院进行标准手术的初始阶段之后,使用计算机生成的序列对医院进行随机化,而不使用分层方法。主要终点是总生存期,根据修改后的意向治疗原则(允许在临床完全缓解时交叉)和意向治疗原则进行分析。非劣效性定义为主动监测的2年生存率低于标准手术的15%。该试验已在荷兰试验登记册(NTR-6803)中注册,纳入阶段已完成。在2017年11月8日至2021年1月17日期间,对1115人进行了筛查,其中309人入选。198人接受了主动监测,111人接受了标准手术。242人(78%)为男性,67人(22%)为女性。中位随访时间为38个月(IQR 32-48)。修改意向治疗分析后,主动监测的2年总生存率(74% [95% CI 69-78])不低于标准手术(71%[62-78])(单侧95%边界:低7%)。意向治疗分析(75% [68-80]vs 70%[63-77],单侧95%边界:低6%)。改良意向治疗分析(风险比1.14,双侧95% CI 0.74 - 1.78)和意向治疗分析(0.83,0.53 - 1.31)的总生存率无显著差异。标准手术或主动监测后延迟手术后的术后并发症发生率和术后死亡率在两组间相似。食管癌主动监测2年后的总生存率与标准手术相比并不差。为了积极监测的长期效果,需要延长随访时间。本试验的结果可用于患者咨询和共同决策。资助荷兰癌症协会(KWF)和荷兰卫生研究与发展组织(ZonMw)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
O-(2-[18F]fluoroethyl)-L-tyrosine-PET-guided versus contrast-enhanced T1-weighted MRI-guided re-irradiation in patients with recurrent glioblastoma (GLIAA/NOA-10 ARO2013-01): a multicentre, open-label, randomised trial Donated sperm with TP53 mutation used to conceive at least 197 children San Antonio Breast Cancer Symposium 2025 Progress in global tobacco control measures UK Government launches first Men's Health Strategy
×
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:604180095
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