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A phase II study of biweekly oxaliplatin plus S-1 combination chemotherapy as a first-line treatment for patients with metastatic or advanced gastric cancer in China

机译:两周一次奥沙利铂联合S-1联合化疗作为中国转移性或晚期胃癌患者一线治疗的II期研究

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摘要

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/m2 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 m2, 1.25–1.5 m2, or >1.5 m2 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.
机译:奥沙利铂加S-1(SOX)是晚期胃癌的一线治疗方案。连续服用S-1 3周可导致不可接受的胃肠道和血液学毒性。因此,为了改善耐受性和非劣效性,有必要采取另一种治疗方案(先服用S-1药物1周,然后休息1周)。我们进行了一项研究,以评估每两周一次SOX作为中国转移性或晚期胃癌患者的一线化疗的疗效和安全性。研究对象包括转移性或先前未治疗的晚期胃癌患者。奥沙利铂在第1天以85mmg / m 2 的剂量静脉内给药,而S-1以80、100或120 mg /天的剂量口服,具体取决于患者体内不同的表面积。分别<1.25 m 2 ,1.25–1.5 m 2 或> 1.5 m 2 ; S-1的总剂量在第1-7天每天两次,然后休息7天。该计划每2周重复一次,直至疾病进展或出现无法忍受的毒性。46例患者(M / F = 33/13)每两周接受一次奥沙利铂和S-1一线化疗。总共进行了257个治疗周期,平均周期数为6。三十六例患者(78.3%)接受了二线化疗。无进展生存中位数和总生存中位数分别为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级不良反应为白细胞减少症(13.04%);贫血(13.04%);中性粒细胞减少症(15.22%);神经毒性(2.17%);腹泻(2.17%)。每两周一次的SOX方案作为一线治疗在中国转移性或晚期胃癌患者中是有效的且耐受性良好。

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