Kamigaichi Atsushi, Hamada Akira, Tsuboi Masahiro, Yoshimura Kenichi, Okamoto Isamu, Yamamoto Nobuyuki, Tsutani Yasuhiro
Department of Surgical Oncology, Hiroshima University, Hiroshima, Japan.
Division of Thoracic Surgery, Department of Surgery, Kindai University, Osaka, Japan.
Clin Lung Cancer. 2024 Jun;25(4):384-388.e1. doi: 10.1016/j.cllc.2024.01.004. Epub 2024 Jan 26.
Although the standard treatment for patients with resectable early-stage non-small-cell lung cancer (NSCLC) is pulmonary lobectomy, recent clinical trials have demonstrated the efficacy of anatomical segmentectomy for small-sized early-stage NSCLC measuring ≤2 cm. Segmentectomy is gaining attention as an alternative procedure to lobectomy for early-stage NSCLC.
In January 2024, we have initiated a randomized phase III trial in Japan to confirm the noninferiority of anatomical segmentectomy to lobectomy in patients with peripheral clinical stage IA3 pure-solid NSCLC (tumor measuring >2 cm and ≤3 cm; consolidation-to-tumor ratio = 1.0). We plan to enroll 520 patients from 61 institutions over a period of 5 years. The primary endpoint is overall survival, and the secondary endpoints include relapse-free survival, postoperative respiratory function, proportion of patients with respiratory failure and cerebrovascular disease, cumulative incidence of death from other diseases, cumulative incidence of local recurrence, proportion of patients who undergo segmentectomy, number of resected segments, operative time, blood loss, and adverse events. This trial has been registered in the UMIN Clinical Trials Registry under the code UMIN000052064.
This trial will help establish a novel treatment strategy for patients with peripheral clinical stage IA3 pure-solid NSCLC.
尽管可切除的早期非小细胞肺癌(NSCLC)患者的标准治疗方法是肺叶切除术,但最近的临床试验已证明,对于直径≤2 cm的小尺寸早期NSCLC,解剖性肺段切除术是有效的。作为早期NSCLC肺叶切除术的替代手术,肺段切除术正受到越来越多的关注。
2024年1月,我们在日本启动了一项随机III期试验,以确认解剖性肺段切除术与肺叶切除术相比,对于外周临床IA3期纯实性NSCLC(肿瘤直径>2 cm且≤3 cm;实性成分与肿瘤比例=1.0)患者是否非劣效。我们计划在5年内从61家机构招募520名患者。主要终点是总生存期,次要终点包括无复发生存期、术后呼吸功能、呼吸衰竭和脑血管疾病患者比例、其他疾病死亡累积发生率、局部复发累积发生率、接受肺段切除术的患者比例、切除段数、手术时间、失血量和不良事件。该试验已在UMIN临床试验注册中心注册,注册号为UMIN000052064。
该试验将有助于为外周临床IA3期纯实性NSCLC患者建立一种新的治疗策略。