Division of Thoracic Surgery, National Cancer Center Hospital East, Kashiwa, Japan.
Department of General Thoracic Surgery, Juntendo University School of Medicine, Tokyo, Japan.
Lancet Respir Med. 2023 Jun;11(6):540-549. doi: 10.1016/S2213-2600(23)00041-3. Epub 2023 Mar 6.
Although segmentectomy is a widely used surgical procedure, lobectomy is the standard procedure for resectable non-small-cell lung cancer (NSCLC). This study aimed to evaluate the efficacy and safety of segmentectomy for NSCLC up to 3 cm in size, including ground-glass opacity (GGO) and predominant GGO.
A multicentre, single-arm, confirmatory phase 3 trial was conducted across 42 institutions (hospitals, university hospitals, and cancer centres) in Japan. Segmentectomy with hilar, interlobar, and intrapulmonary lymph node dissection was performed as protocol surgery for patients with a tumour diameter of up to 3 cm, including GGO and dominant GGO. Eligible patients were those aged 20-79 years with an Eastern Cooperative Oncology Group performance score of 0 or 1 and clinical stage IA tumour confirmed by thin-sliced CT. The primary endpoint was 5-year relapse-free survival (RFS). This study is registered with the University Hospital Medical Information Network Clinical Trials (UMIN000011819), and is ongoing.
A total of 396 patients were registered from Sept 20, 2013, to Nov 13, 2015, of whom 357 underwent segmentectomy. At a median follow-up of 5·4 years (IQR 5·0-6·0), the 5-year RFS was 98·0% (95% CI 95·9-99·1). This finding exceeded the 87% of the pre-set threshold 5-year RFS and the primary endpoint was met. Grade 3 or 4 early postoperative complications occurred in seven patients (2%), but no grade 5 treatment-related deaths occurred.
Segmentectomy should be considered as part of standard treatment for patients with predominantly GGO NSCLC with a tumour size of 3 cm or less in diameter, including GGO even if it exceeds 2 cm.
National Cancer Centre Research and Development Fund and Japan Agency for Medical Research and Development.
虽然肺段切除术是一种广泛应用的手术方法,但肺叶切除术是可切除的非小细胞肺癌(NSCLC)的标准手术。本研究旨在评估最大直径达 3cm 的 NSCLC 行肺段切除术(包括磨玻璃密度影[GGO]和以 GGO 为主的病变)的疗效和安全性。
本研究在日本的 42 家机构(医院、大学医院和癌症中心)进行了一项多中心、单臂、确证性 III 期临床试验。对于肿瘤直径达 3cm 及以下、包括 GGO 和以 GGO 为主的病变的患者,行肺段切除术加肺门、叶间和肺内淋巴结清扫作为标准术式。纳入标准为年龄 20-79 岁,东部肿瘤协作组体能状态评分为 0 或 1 分,且临床分期为 IA 期的薄层 CT 证实的肿瘤。主要终点为 5 年无复发生存率(RFS)。本研究在日本大学医院医疗信息网络临床试验注册平台(UMIN000011819)进行,正在进行中。
从 2013 年 9 月 20 日至 2015 年 11 月 13 日,共登记了 396 例患者,其中 357 例行肺段切除术。中位随访 5.4 年(IQR 5.0-6.0)时,5 年 RFS 为 98.0%(95%CI 95.9-99.1)。这一结果超过了预设的 5 年 RFS 阈值 87%,主要终点达到。7 例(2%)患者发生 3 级或 4 级早期术后并发症,但无 5 级与治疗相关的死亡。
对于最大直径达 3cm 的以 GGO 为主的 NSCLC 患者(包括 GGO 直径超过 2cm 的患者),肺段切除术应作为标准治疗的一部分。
国家癌症中心研究与发展基金和日本医疗研究与发展机构。