The role of preoperative immunonutrition on morbidity and immune response after cystectomy: protocol of a multicenter randomized controlled trial (INCyst Trial).

IF 2 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Trials Pub Date : 2024-10-17 DOI:10.1186/s13063-024-08536-5
Laurent Derré, François Crettenand, Nuno Grilo, Kevin Stritt, Bernhard Kiss, Thomas Tawadros, Sonia Domingos-Pereira, Beat Roth, Yannick Cerantola, Ilaria Lucca
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引用次数: 0

Abstract

Introduction: Cancer, malnutrition, and surgery negatively impact patient's immune system. Despite standardized surgical technique and the development of new perioperative care protocols, morbidity after cystectomy remains a serious challenge for urologists. Most common postoperative complications, such as infections and ileus, often lead to longer length of stay and worse survival. The immune system and its interaction with the gut microbiota play a pivotal role in cancer immunosurveillance and in patient's response to surgical stress. Malnutrition has been identified as an independent and modifiable risk factor for both mortality and morbidity. Immunonutrition (IN) may improve the nutritional status, immunological function, and clinical outcome of surgical patients. Aims of the study are (1) to evaluate the impact of IN on morbidity and mortality at 30 and 90 days after cystectomy and (2) to determine immune and microbiota signature that would predict IN effect.

Methods: This is a randomized, multicentric, controlled, pragmatic, parallel-group comparative study, supported by the Swiss National Science Foundation. A total of 232 patients is planned to be enrolled between April 2023 and June 2026. Three participating centers (Lausanne, Bern, and Riviera-Chablais) have been selected. All patients undergoing elective radical and simple cystectomy will be randomly assigned to receive 7 days of preoperative IN (Oral Impact®, Nestlé, Switzerland) versus standard of care (control group) and followed for 90 days after surgery. For the exploratory outcomes, blood, serum, urine, and stool samples will be collected in patients treated at Lausanne. In order to determine the impact of IN on immune fitness, patients enrolled at Lausanne will be vaccinated against influenza and the establishment of the vaccine-specific immune response will be followed. Analysis of the microbiota and expression of argininosuccinate synthetase 1 as potential biomarker will also be performed.

Discussion and conclusion: Strengths of the INCyst study include the randomized, multicenter, prospective design, the large number of patients studied, and the translational investigation. This study will challenge the added value of preoperative IN in patients undergoing cystectomy, assessing the clinical effect of IN on the onset of postoperative morbidity and mortality after cystectomy. Furthermore, it will provide invaluable data on the host immune response and microbiota composition.

Trial registration: ClinicalTrials.gov NCT05726786. Registered on March 9, 2023.

术前免疫营养对膀胱切除术后发病率和免疫反应的作用:多中心随机对照试验(INCyst 试验)方案。
简介癌症、营养不良和手术会对患者的免疫系统产生负面影响。尽管采用了标准化的手术技术并制定了新的围手术期护理方案,但膀胱切除术后的发病率仍是泌尿科医生面临的严峻挑战。最常见的术后并发症,如感染和回肠梗阻,往往导致住院时间延长和生存率降低。免疫系统及其与肠道微生物群的相互作用在癌症免疫监视和患者对手术压力的反应中起着关键作用。营养不良已被确定为死亡率和发病率的一个独立且可改变的风险因素。免疫营养(IN)可改善手术患者的营养状况、免疫功能和临床效果。本研究的目的是:(1) 评估膀胱切除术后 30 天和 90 天免疫营养对发病率和死亡率的影响;(2) 确定可预测免疫营养效果的免疫和微生物群特征:这是一项由瑞士国家科学基金会支持的随机、多中心、对照、实用、平行组比较研究。计划在 2023 年 4 月至 2026 年 6 月期间招募 232 名患者。目前已选定三个参与中心(洛桑、伯尔尼和里维埃拉-卡布赖)。所有接受根治性和单纯性膀胱切除术的患者将被随机分配到接受术前 7 天 IN(Oral Impact®,瑞士雀巢公司)治疗与标准治疗(对照组),并在术后随访 90 天。对于探索性结果,将收集在洛桑接受治疗的患者的血液、血清、尿液和粪便样本。为了确定 IN 对免疫力的影响,洛桑医院的入组患者将接种流感疫苗,并跟踪疫苗特异性免疫反应的建立情况。此外,还将对微生物群和作为潜在生物标志物的精氨酸琥珀酸合成酶1的表达进行分析:INCyst 研究的优势包括随机、多中心、前瞻性设计、研究的患者人数众多以及转化研究。这项研究将对膀胱切除术患者术前 IN 的附加价值提出质疑,评估 IN 对膀胱切除术后发病率和死亡率的临床影响。此外,它还将提供有关宿主免疫反应和微生物群组成的宝贵数据:试验注册:ClinicalTrials.gov NCT05726786。注册日期:2023 年 3 月 9 日。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Trials
Trials 医学-医学:研究与实验
CiteScore
3.80
自引率
4.00%
发文量
966
审稿时长
6 months
期刊介绍: Trials is an open access, peer-reviewed, online journal that will encompass all aspects of the performance and findings of randomized controlled trials. Trials will experiment with, and then refine, innovative approaches to improving communication about trials. We are keen to move beyond publishing traditional trial results articles (although these will be included). We believe this represents an exciting opportunity to advance the science and reporting of trials. Prior to 2006, Trials was published as Current Controlled Trials in Cardiovascular Medicine (CCTCVM). All published CCTCVM articles are available via the Trials website and citations to CCTCVM article URLs will continue to be supported.
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