Han Yu, Zhang Weixun, Xu Peihang, Tian Zhoujunyi, Hao Yang, Zhang Jin, Ren Tai, Liang Chaoyang
Department of General Thoracic Surgery, China-Japan Friendship Hospital, Beijing, China.
Ministry of Education-Shanghai Key Laboratory of Children's Environmental Health, Department of Developmental and Behavioural Paediatric & Child Primary Care, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
BMC Surg. 2025 Jan 27;25(1):45. doi: 10.1186/s12893-024-02753-0.
Previous retrospective studies demonstrated both one-stage and two-stage video-assisted thoracic surgery (VATS) for bilateral pulmonary nodules were safe and feasible in selected patients. However, prospective data is still lacking. The purpose of this trial is to prospectively compare the prognostic and perioperative outcomes between one-stage and two-stage VATS for synchronous bilateral pulmonary nodules.
We conduct a prospective clinical trial to investigate the surgical outcomes of one-stage and two-stage VATS for patients with synchronous bilateral pulmonary nodules. This trial plan to enroll 198 patients from a single institution during a period of 5 years. The primary outcome is 5-year overall survival. Secondary outcomes include 5-year disease free survival, 3-year overall survival, 3-year disease free survival, overall complications rate, 30-day mortality, pain score after surgery, surgical time, blood loss in the operation, duration of chest tube, length of stay, and quality of life score after surgery.
To our knowledge, this study is the first prospective registered clinical trials to compare the clinical outcomes after one-stage or two-stage VATS for synchronous bilateral non-small cell lung cancer.
This study underwent review by the Ethics Committee of China-Japan Friendship Hospital under No. 2023-KY-061-1. It has been officially registered with the China Clinical Trial Registry, TRN: ChiCTR2300071198 and registration date is May. 8, 2023.
既往回顾性研究表明,对于双侧肺结节患者,一期和二期电视辅助胸腔镜手术(VATS)在特定患者中都是安全可行的。然而,前瞻性数据仍然缺乏。本试验的目的是前瞻性比较一期和二期VATS治疗同步双侧肺结节的预后和围手术期结果。
我们开展一项前瞻性临床试验,以研究一期和二期VATS治疗同步双侧肺结节患者的手术结果。本试验计划在5年内从单一机构招募198例患者。主要结局是5年总生存率。次要结局包括5年无病生存率、3年总生存率、3年无病生存率、总体并发症发生率、30天死亡率、术后疼痛评分、手术时间、术中失血量、胸管留置时间、住院时间以及术后生活质量评分。
据我们所知,本研究是第一项比较一期或二期VATS治疗同步双侧非小细胞肺癌临床结局的前瞻性注册临床试验。
本研究已通过中日友好医院伦理委员会审查,编号为2023-KY-061-1。已在中国临床试验注册中心正式注册,注册号:ChiCTR2300071198,注册日期为2023年5月8日。