Kawase Tomono, Imamura Hiroshi, Kawabata Ryohei, Matsuyama Jin, Nishikawa Kazuhiro, Yanagihara Kazuhiro, Yamamoto Kazuyoshi, Hoki Noriyuki, Kawada Junji, Kawakami Hisato, Sakai Daisuke, Kurokawa Yukinori, Shimokawa Toshio, Satoh Taroh
Department of Surgery, Toyonaka Municipal Hospital, 4-14-1 Shibahara-cho, Toyonaka-city, Japan.
Department of Surgery, Sakai City Medical Center, 1-1-1 Ebaraji-cho, Nishi-ku, Sakai-city, Japan.
Int J Clin Oncol. 2024 Feb;29(2):134-141. doi: 10.1007/s10147-023-02437-4. Epub 2024 Jan 16.
Although there is insufficient evidence for the treatment of older patients with advanced gastric cancer, fluorouracil combined with platinum chemotherapy has been recognized as a standard first-line treatment for such populations in Japan despite the lack of efficacy and toxicity data.
Patients aged 75 years or older with advanced gastric cancer were enrolled. S-1 plus docetaxel (docetaxel: 40 mg/m, day 1; S-1: 80 mg/m, days 1-14; q21 days) was repeated every 3 weeks. The primary endpoint was overall response rate. Secondary endpoints were safety, progression-free survival, time to treatment failure, and overall survival. The sample size was calculated as 30 under the hypothesis of an expected response rate of 40% and a threshold response rate of 20%, at a power of 90% and a two-sided alpha value of 5%.
From February 2010 to January 2015, 31 patients were enrolled and assessed for efficacy and toxicity. The response rate was 45.2% (95% CI 27.3%-64.0%; p = 0.001) and it exceeded the expected response rate set at 40%. Median progression-free survival was 5.8 months, the 1-year survival rate was 58.1%, and the median survival time was 16.1 months. The major grade 3/4 adverse events were neutropenia (58%), febrile neutropenia (13%), anemia (10%), anorexia (10%), and fatigue (6%).
These findings indicate that S-1 plus docetaxel as first-line treatment for older patients is feasible and that it has promising efficacy against advanced gastric cancer.
尽管对于老年晚期胃癌患者的治疗证据不足,但在日本,氟尿嘧啶联合铂类化疗已被视为这类人群的标准一线治疗方案,尽管缺乏疗效和毒性数据。
纳入年龄在75岁及以上的晚期胃癌患者。每3周重复使用S-1联合多西他赛(多西他赛:40mg/m²,第1天;S-1:80mg/m²,第1 - 14天;每21天一个周期)。主要终点是总缓解率。次要终点是安全性、无进展生存期、治疗失败时间和总生存期。在预期缓解率为40%、阈值缓解率为20%、检验效能为90%和双侧α值为5%的假设下,样本量计算为30例。
2010年2月至2015年1月,共纳入31例患者并评估其疗效和毒性。缓解率为45.2%(95%置信区间27.3% - 64.0%;p = 0.001),超过了设定的40%的预期缓解率。中位无进展生存期为5.8个月,1年生存率为58.1%,中位生存时间为16.1个月。主要的3/4级不良事件为中性粒细胞减少(58%)、发热性中性粒细胞减少(13%)、贫血(10%)、厌食(10%)和疲劳(6%)。
这些结果表明,S-1联合多西他赛作为老年患者的一线治疗方案是可行的,并且对晚期胃癌具有良好的疗效。