Xiao Cheng, Qian Jiong, Zheng Yulong, Song Fang, Wang Qiangfeng, Jiang Haiping, Mao Chenyu, Xu Nong
Department of Medical Oncology.
Department of Anesthesiology, the First Affiliated Hospital of Zhejiang University, Hangzhou, China.
Medicine (Baltimore). 2019 May;98(20):e15696. doi: 10.1097/MD.0000000000015696.
Oxaliplatin plus S-1 (SOX) was a first-line regimen for advanced gastric cancer. The continuous administration of S-1 for 3 weeks can result in unacceptable gastrointestinal and hematological toxicities. Therefore, an alternative regimen (administration of S-1 for 1-week followed by 1-week rest) is warrant for improved tolerability and noninferiority efficacy. We conducted a study to evaluate the efficacy and safety of biweekly SOX as the first-line chemotherapy in patients with metastatic or advanced gastric cancer in China.Patients with metastatic or previously untreated advanced gastric cancer were enrolled. Oxaliplatin was administered intravenously at a dose of 85 mg/m on day 1, while S-1 was administered orally in doses of 80, 100, or 120 mg/day depending on different body surface areas of <1.25 m, 1.25-1.5 m, or >1.5 m respectively; the total dose of S-1 was administered twice daily on days 1-7 followed by a 7-day rest. This schedule was repeated every 2 weeks until disease progressed or intolerable toxicity occurred.Forty-six patients (M/F = 33/13) received biweekly oxaliplatin and S-1 as first-line chemotherapy. A total of 257 treatment cycles were administered and the median number of cycles administered was 6. Thirty-six patients (78.3%) received second-line chemotherapy. The median progression free survival and median overall survival was 4.4 months (95% CI, 3.37-5.36 months) and 10.3 months (95% CI, 8.88-11.3 months), respectively. The 1-year and 2-year survival rate was 41% and 13%. The objective response rate was 30.43%, and the disease control rate was 76.08%. The observed adverse events of Grade 3/4 included were leukocytopenia (13.04%); anemia (13.04%); neutropenia (15.22%); neurological toxicity (2.17%); diarrhea (2.17%).The biweekly SOX regimen as first-line treatment was active and well tolerated in Chinese patients with metastatic or advanced gastric cancer.
奥沙利铂联合S-1(SOX)是晚期胃癌的一线治疗方案。连续3周服用S-1会导致难以接受的胃肠道和血液学毒性。因此,需要一种替代方案(服用S-1 1周后休息1周)以提高耐受性并获得非劣效性疗效。我们开展了一项研究,以评估在中国转移性或晚期胃癌患者中,每2周进行一次SOX一线化疗的疗效和安全性。
纳入转移性或既往未接受过治疗的晚期胃癌患者。奥沙利铂于第1天静脉注射,剂量为85mg/m²,而S-1根据不同体表面积分别以80、100或120mg/天的剂量口服,体表面积<1.25m²、1.25 - 1.5m²或>1.5m²;S-1总剂量在第1 - 7天每日分两次服用,随后休息7天。每2周重复此方案,直至疾病进展或出现无法耐受的毒性。
46例患者(男/女 = 33/13)接受了每2周一次的奥沙利铂和S-1一线化疗。共进行了257个治疗周期,中位治疗周期数为6个。36例患者(78.3%)接受了二线化疗。中位无进展生存期和中位总生存期分别为4.4个月(95%CI,3.37 - 5.36个月)和10.3个月(95%CI,8.88 - 11.3个月)。1年和2年生存率分别为41%和13%。客观缓解率为30.43%,疾病控制率为76.08%。观察到的3/4级不良事件包括白细胞减少(13.04%);贫血(13.04%);中性粒细胞减少(15.22%);神经毒性(2.17%);腹泻(2.17%)。
每2周进行一次SOX方案作为一线治疗,在中国转移性或晚期胃癌患者中具有活性且耐受性良好。