Takashima Yusuke, Komatsu Shuhei, Nishibeppu Keiji, Kiuchi Jun, Ohashi Takuma, Shimizu Hiroki, Arita Tomohiro, Yamamoto Yusuke, Konishi Hirotaka, Morimura Ryo, Shiozaki Atsushi, Kuriu Yoshiaki, Ikoma Hisashi, Kubota Takeshi, Fujiwara Hitoshi, Okamoto Kazuma, Otsuji Eigo
Division of Digestive Surgery, Department of Surgery, Kyoto Prefectural University of Medicine, 465 Kajii-cho, Kawaramachihirokoji, Kamigyo-ku, Kyoto, Japan.
J Cancer. 2021 Aug 13;12(19):5960-5966. doi: 10.7150/jca.58154. eCollection 2021.
Adjuvant chemotherapy (AC) following curative gastrectomy for stage II/III gastric cancer (GC) is recommended in Japan. However, for various reasons, patients cannot always start AC at the appropriate time. This study was designed to investigate the effect of the postoperative interval until adjuvant chemotherapy (PIAC) and cumulative S-1 dose on prognosis. Between 2008 and 2014, consecutive 81 GC patients who underwent postoperative S-1 monotherapy were enrolled in this study. Postoperative complications of Clavien-Dindo grade II or higher and postoperative peak C-reactive protein of 8.1 mg/dl or higher were significantly associated with delayed AC. The cut-off value of PIAC selected to most effectively stratify prognosis was 7 weeks. For relapse-free survival (RFS), patients with PIAC ≥ 7 weeks had an insignificantly poorer prognosis than those with PIAC < 7 weeks. A multivariate analysis showed that PIAC ≥ 7 weeks [ = 0.024; hazard ratio (HR) 2.45] and the cumulative S-1 dose/body surface area (BSA) ≥ 12,000 mg/m [ = 0.004; HR 3.27] were independent prognostic factors. In patients with the cumulative S-1 dose/BSA ≥ 12,000 mg/m, there were no prognostic differences between patients with and without PIAC ≥ 7 weeks. Seven weeks after surgery could be a limit indicator starting AC. A cumulative S-1 dose/BSA of more than 12,000 mg/m might be a key dose for diminishing the poor prognostic effects of delaying AC.
在日本,对于II/III期胃癌(GC)患者,根治性胃切除术后推荐进行辅助化疗(AC)。然而,由于各种原因,患者并非总能在适当的时间开始AC。本研究旨在探讨辅助化疗术后间隔时间(PIAC)和S-1累积剂量对预后的影响。2008年至2014年期间,连续81例接受术后S-1单药治疗的GC患者纳入本研究。Clavien-Dindo分级II级或更高的术后并发症以及术后C反应蛋白峰值8.1mg/dl或更高与AC延迟显著相关。为最有效分层预后而选择的PIAC临界值为7周。对于无复发生存期(RFS),PIAC≥7周的患者预后略差于PIAC<7周的患者。多因素分析显示,PIAC≥7周[ = 0.024;风险比(HR)2.45]和S-1累积剂量/体表面积(BSA)≥12,000mg/m[ = 0.004;HR 3.27]是独立的预后因素。在S-1累积剂量/BSA≥12,000mg/m的患者中,PIAC≥7周和未≥7周的患者之间无预后差异。术后7周可能是开始AC的极限指标。S-1累积剂量/BSA超过12,000mg/m可能是减少延迟AC不良预后影响的关键剂量。