Leroy Sylvie, Benzaquen Jonathan, Mazzetta Andrea, Marchand-Adam Sylvain, Padovani Bernard, Israel-Biet Dominique, Pison Christophe, Chanez Pascal, Cadranel Jacques, Mazières Julien, Jounieaux Vincent, Cohen Charlotte, Hofman Véronique, Ilie Marius, Hofman Paul, Marquette Charles Hugo
Department of Pulmonary Medicine and Thoracic Oncology, Centre Hospitalier Universitaire de Nice, Nice, France.
CNRS, INSERM, IPMC, FHU-OncoAge, Université Côte d'Azur, Valbonne, France.
BMJ Open. 2017 Dec 26;7(12):e018884. doi: 10.1136/bmjopen-2017-018884.
Lung cancer (LC) is the leading cause of death from cancer. Early diagnosis of LC is of paramount importance in terms of prognosis. The health authorities of most countries do not accept screening programmes based on low-dose chest CT (LDCT), especially in Europe, because they are flawed by a high rate of false-positive results, leading to a large number of invasive diagnostic procedures. These authorities advocated further research, including companion biological tests that could enhance the effectiveness of LC screening. The present project aims to validate early diagnosis of LC by detection and characterisation of circulating tumour cells (CTCs) in a peripheral blood sample taken from a prospective cohort of persons at high-risk of LC.
The AIR Project is a prospective, multicentre, double-blinded, cohort study conducted by a consortium of 21 French university centres. The primary objective is to determine the operational values of CTCs for the early detection of LC in a cohort of asymptomatic participants at high risk for LC, that is, smokers and ex-smokers (≥30 pack-years, quitted ≤15 years), aged ≥55 years, with chronic obstructive pulmonary disease (COPD). The study participants will undergo yearly screening rounds for 3 years plus a 1-year follow-up. Each round will include LDCT plus peripheral blood sampling for CTC detection. Assuming 5% prevalence of LC in the studied population and a 10% dropout rate, a total of at least 600 volunteers will be enrolled.
The study sponsor is the University Hospital of Nice. The study was approved for France by the ethical committee CPP Sud-Méditerranée V and the ANSM (Ministry of Health) in July 2015. The findings of the trial will be disseminated through peer-reviewed journals and national and international conference presentations.
NCT02500693.
肺癌是癌症死亡的主要原因。肺癌的早期诊断对预后至关重要。大多数国家的卫生当局不接受基于低剂量胸部CT(LDCT)的筛查项目,尤其是在欧洲,因为这些项目存在较高的假阳性率,导致大量侵入性诊断程序。这些当局主张进一步开展研究,包括使用辅助生物学检测,以提高肺癌筛查的有效性。本项目旨在通过检测和表征从肺癌高危人群前瞻性队列采集的外周血样本中的循环肿瘤细胞(CTC)来验证肺癌的早期诊断。
AIR项目是一项由21个法国大学中心组成的联盟进行的前瞻性、多中心、双盲队列研究。主要目标是确定在一组无症状的肺癌高危参与者(即吸烟者和戒烟者(≥30包年,戒烟≤15年),年龄≥55岁,患有慢性阻塞性肺疾病(COPD))中,CTC用于肺癌早期检测的实用价值。研究参与者将接受为期3年的年度筛查轮次以及1年的随访。每一轮筛查将包括LDCT加上用于CTC检测的外周血采样。假设研究人群中肺癌患病率为5%,失访率为10%,总共至少将招募600名志愿者。
研究主办方是尼斯大学医院。该研究于2015年7月获得法国伦理委员会CPP Sud-Méditerranée V和法国国家药品安全局(卫生部)批准。试验结果将通过同行评审期刊以及在国内和国际会议上发表进行传播。
NCT02500693。