Toyokawa Takahiro, Tamura Tatsuro, Shibutani Masatsune, Ohira Goh, Yamazoe Sadaaki, Kimura Kenjiro, Nagahara Hisashi, Amano Ryosuke, Tanaka Hiroaki, Muguruma Kazuya, Yashiro Masakazu, Hirakawa Kosei, Ohira Masaichi
Dept. of Surgical Oncology, Osaka City University Graduate School of Medicine.
Gan To Kagaku Ryoho. 2017 May;44(5):405-408.
We retrospectively investigated the efficacy and safety of S-1 and oxaliplatin(SOX)as the first-line chemotherapy in patients with metastatic/recurrent gastric cancer. A total of 27 patients who received SOX as the first-line chemotherapy in our hospital were considered for the study. The SOX chemotherapy schedule consisted of 1 course every 3 weeks. S-1 was administered orally, at 80-120mg-body, every day for 14 days. Oxaliplatin was infused at 100mg/m2 on day 1 of each course. The median number of treatment courses was 7. The response rate and disease control rate were 47.6% and 76.2%, respectively. The observed adverse events of Grade 3 or more included neutropenia(33.3%); peripheral neuropathy and anorexia(11.1%); thrombocytopenia(7.4%); and anemia, diarrhea, fatigue, and hypercalcemia(3.7%). The median overall survival was not achieved, and the 1-year survival rate was 63.2%. Therefore, SOX is an effective and feasible first-line chemotherapy that is easily available for ambulatory treatment of patients with metastatic/recurrent gastric cancer.
我们回顾性研究了S-1与奥沙利铂(SOX)作为转移性/复发性胃癌患者一线化疗的疗效和安全性。共有27例在我院接受SOX一线化疗的患者纳入本研究。SOX化疗方案为每3周1个疗程。S-1口服给药,剂量为80 - 120mg/体质量,每日1次,共14天。奥沙利铂在每个疗程的第1天以100mg/m²静脉滴注。治疗疗程的中位数为7个。有效率和疾病控制率分别为47.6%和76.2%。观察到的3级及以上不良事件包括中性粒细胞减少(33.3%);周围神经病变和厌食(11.1%);血小板减少(7.4%);以及贫血、腹泻、乏力和高钙血症(3.7%)。总生存期中位数未达到,1年生存率为63.2%。因此,SOX是一种有效且可行的一线化疗方案,便于门诊治疗转移性/复发性胃癌患者。