Division of Gastric Surgery, Shizuoka Cancer Center, Nagaizumi, Japan.
Department of Gastric Surgery, National Cancer Center Hospital, Tokyo, Japan.
Jpn J Clin Oncol. 2020 May 5;50(5):528-534. doi: 10.1093/jjco/hyaa005.
Perioperative treatment for locally advanced gastric cancer has been inconsistent between Japan and the Western countries. In Japan, D2 gastrectomy followed by adjuvant chemotherapy is regarded as standard treatment, while neoadjuvant or perioperative chemotherapy is considered to be a standard in the Western countries. Stomach Cancer Study Group of Japan Clinical Oncology Group (JCOG) has conducted many perioperative chemotherapy trials. After the publishing of positive results of ACTS-GC trial, stage-specific adjuvant chemotherapy protocols are planned. JCOG1104 was conducted as to demonstrate the non-inferiority of four courses of S-1 to standard eight courses of S-1, because the efficacy of S-1 appears to be sufficient in stage II. The trial failed to demonstrate the non-inferiority of four courses of S-1. S-1 for 1 year is still recognized to be a standard for stage II gastric cancer. For stage III, studies with more intensive treatments were planned as the efficacy of S-1 monotherapy seems to be insufficient. As in the Western countries, JCOG planned the perioperative chemotherapy. However, the clinical staging is a serious issue to select optimal patients for perioperative chemotherapy. JCOG conducted a prospective cohort study to evaluate the validity of clinical staging in JCOG1302A. From the results of this study, cT3-4 and cN1-3 are selected as optimal candidate for perioperative chemotherapy. JCOG1509 was conducted to demonstrate the superiority of perioperative chemotherapy to adjuvant chemotherapy in these cohorts. Perioperative chemotherapy for marginally resectable tumours such as linitis plastica or extensive nodal disease and special type of cancer like HER2 positive are also conducted.
局部进展期胃癌的围手术期治疗在日本和西方国家之间存在差异。在日本,D2 胃切除术加辅助化疗被视为标准治疗,而新辅助或围手术期化疗被认为是西方国家的标准治疗。日本临床肿瘤学组(JCOG)进行了许多围手术期化疗试验。在 ACTS-GC 试验的阳性结果公布后,计划制定基于分期的辅助化疗方案。JCOG1104 旨在证明四疗程 S-1 与标准八疗程 S-1 的非劣效性,因为 S-1 在 II 期的疗效似乎已经足够。该试验未能证明四疗程 S-1 的非劣效性。S-1 治疗 1 年仍被认为是 II 期胃癌的标准治疗。对于 III 期,由于 S-1 单药治疗的疗效似乎不足,计划进行更强化治疗的研究。与西方国家一样,JCOG 计划进行围手术期化疗。然而,临床分期是选择围手术期化疗最佳患者的一个严重问题。JCOG 进行了一项前瞻性队列研究,以评估 JCOG1302A 中临床分期的有效性。该研究结果表明,cT3-4 和 cN1-3 是围手术期化疗的最佳候选者。JCOG1509 旨在证明这些队列中围手术期化疗优于辅助化疗的优越性。对于边缘可切除肿瘤(如皮革胃或广泛淋巴结转移)和特殊类型的癌症(如 HER2 阳性),也进行了围手术期化疗。