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非小细胞肺癌表现为磨玻璃结节的 IA 期纵隔淋巴结清扫与保留纵隔淋巴结清扫的比较:中国一项 III 期、随机、多中心试验(MELDSIG)的研究方案。

Mediastinal lymph node dissection versus spared mediastinal lymph node dissection in stage IA non-small cell lung cancer presented as ground glass nodules: study protocol of a phase III, randomised, multicentre trial (MELDSIG) in China.

机构信息

Department of Lung Cancer, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin's Clinical Research Center for Cancer, Tianjin, China.

Department of Thoracic Surgery, Air Force Medical University Tangdu Hospital, Xi'an, Shanxi, China.

出版信息

BMJ Open. 2023 Oct 28;13(10):e075242. doi: 10.1136/bmjopen-2023-075242.

Abstract

INTRODUCTION

Radical surgery including mediastinal lymph node dissection is the standard treatment for early-stage non-small cell lung cancer (NSCLC). About 50% lung nodules are pure ground glass or part-solid nodules, which are predominantly clinical stage IA NSCLC. Non-solid nodules rarely develop mediastinal lymph node metastasis.

METHOD AND ANALYSIS

A phase III study was started in China to evaluate the non-inferiority in overall survival of spared mediastinal lymph node dissection compared with mediastinal lymph node dissection in stage IA NSCLC. A total of 1362 patients will be enrolled from 4 institutions in 2-3 years. The second endpoints are relapse-free survival and perioperative data, including duration of hospitalisation, duration of chest tube placement, operation time, blood loss.

ETHICS AND DISSEMINATION

This protocol has been reviewed and approved by the Clinical Research Review Board of Tianjin Medical University Cancer Institute and Hospital. The findings will be disseminated in peer-reviewed publications.

TRIAL REGISTRATION NUMBER

NCT04631770.

摘要

简介

根治性手术包括纵隔淋巴结清扫术是非小细胞肺癌(NSCLC)早期的标准治疗方法。大约 50%的肺结节为纯磨玻璃或部分实性结节,主要为临床ⅠA 期 NSCLC。非实性结节很少发生纵隔淋巴结转移。

方法与分析

中国已开始进行一项 III 期研究,以评估 IA 期 NSCLC 纵隔淋巴结保留清扫术与纵隔淋巴结清扫术在总生存方面的非劣效性。预计将在 2-3 年内从 4 家机构招募 1362 名患者。次要终点是无复发生存期和围手术期数据,包括住院时间、胸腔引流管放置时间、手术时间、出血量。

伦理与传播

本方案已由天津医科大学肿瘤医院临床研究审查委员会审查和批准。研究结果将在同行评议的出版物中发表。

临床试验注册编号

NCT04631770。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a99/10619047/a1d64273bbdc/bmjopen-2023-075242f01.jpg

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