Zhong Dong-ta, Wu Ri-ping, Wang Xin-li, Huang Xiao-bing, Lin Meng-xin, Lan Yan-qin, Chen Qiang
Department of Medical Oncology, Fujian Medical University Union Hospital, No. 29 Xinquan Road, Fuzhou, 350001, Fujian, People's Republic of China.
Pathol Oncol Res. 2015 Sep;21(4):867-73. doi: 10.1007/s12253-015-9903-1. Epub 2015 Feb 4.
This study is a retrospective analysis evaluating the efficacy and toxicity of combination chemotherapy with S-1 and oxaliplatin (SOX) as first-line treatment in elderly patients with advanced gastric cancer. One hundred and twenty-nine patients with recurrent or metastatic gastric adenocarcinoma were treated with SOX; S-1 (40-60 mg depending on patient's body surface area) was given orally, twice daily on days 1 to 14 followed by a 7-day rest period, 130 mg/m(2) oxaliplatin was given as an intravenous infusion over 2-hours on day one. The cycle was repeated every three weeks. All of the patients were older than 65 years. Among 129 patients enrolled, nine patients could not be evaluated for responses because of the absence of any measurable lesions or early discontinuation of therapy. Assessment of the response of 120 patients was made. The overall objective response rate was 54.2 % (95 %CI, 45.3-63.1 %), with three complete responses and 62 partial responses. The disease control rate was 80.8 % (95 %CI, 73.8-87.8 %). The median follow-up period was 23 months (range, 5-42 months). The median time to progression was 6.9 months (95 %CI, 5.5-8.3 months) and the median overall survival was 12.8 months (95 %CI, 11.4-14.2 months). The one-year survival rate was 57.5 % (95 %CI, 48.7-66.3 %). In 129 patients assessed safety, grade 3 and 4 toxicities included leucopenia (20.9 %), neutropenia (24.0 %), anemia (10.9 %), thrombocytopenia (10.1 %), anorexia (3.1 %), peripheral neurotoxicity (15.5 %), and fatigue (12.4 %). No treatment-related deaths occurred. Combination chemotherapy with SOX offers an effective, safe and well-tolerated regimen for elderly patients with advanced gastric cancer.
本研究是一项回顾性分析,旨在评估S-1与奥沙利铂联合化疗(SOX)作为老年晚期胃癌患者一线治疗的疗效和毒性。129例复发性或转移性胃腺癌患者接受了SOX治疗;S-1(根据患者体表面积给予40-60mg)口服,第1至14天每天两次,随后休息7天,第1天静脉输注130mg/m²奥沙利铂,持续2小时。每三周重复一个周期。所有患者年龄均超过65岁。在纳入的129例患者中,9例因无任何可测量病灶或提前终止治疗而无法评估疗效。对120例患者的疗效进行了评估。总体客观缓解率为54.2%(95%CI,45.3-63.1%),其中3例完全缓解,62例部分缓解。疾病控制率为80.8%(95%CI,73.8-87.8%)。中位随访期为23个月(范围5-42个月)。中位疾病进展时间为6.9个月(95%CI,5.5-8.3个月),中位总生存期为12.8个月(95%CI,11.4-14.2个月)。一年生存率为57.5%(95%CI,48.7-66.3%)。在129例接受安全性评估的患者中,3级和4级毒性包括白细胞减少(20.9%)、中性粒细胞减少(24.0%)、贫血(10.9%)、血小板减少(10.1%)、厌食(3.1%)、周围神经毒性(15.5%)和疲劳(12.4%)。未发生与治疗相关的死亡。SOX联合化疗为老年晚期胃癌患者提供了一种有效、安全且耐受性良好的治疗方案。