Cheng Xiao-Wei, Leng Wen-Hua, Mu Chun-Ling
Department of Respiratory and Critical Care Medicine, Panzhihua Central Hospital, Panzhihua 617067, Sichuan Province, China.
Department of Ultrasound, Panzhihua Central Hospital, Panzhihua 617067, Sichuan Province, China.
World J Clin Cases. 2020 Nov 6;8(21):5172-5179. doi: 10.12998/wjcc.v8.i21.5172.
Previous reports have demonstrated that S-1 has remarkable effects in the maintenance treatment of advanced non-small-cell lung cancer (NSCLC), and has less toxic and side effects than conventional drugs.
To investigate the efficacy and safety of S-1 maintenance therapy in patients with advanced NSCLC.
Ninety-four patients with NSCLC admitted to our hospital from September 2015 to April 2018 were included in the study and divided into the S-1 group (47 cases) and the gemcitabine group (47 cases) by random digital table method. The S-1 group was treated with S-1, while the gemcitabine group received gemcitabine treatment. The clinical efficacy and quality of life of the patients after treatment in the two groups were evaluated.
There was no significant difference in the total effectiveness rate between the two groups ( = 0.519). The quality-of-life scores indicated that there was no significant difference between the two groups in terms of four dimensions of the GQOLI-74 questionnaire ( = 0.518, 0.094, 0.338, 0.418). The incidence of nausea and vomiting, granulocytopenia and diarrhea in the S-1 group was significantly lower than that in the gemcitabine group ( = 0.001, 0.001 and 0.001, respectively). There was no significant difference in the incidence of thrombocytopenia ( = 0.366), the progression-free survival ( = 0.064), and the survival between the two groups ( = 0.050).
S-1 maintenance therapy shows a significant therapeutic effect in patients with advanced NSCLC. It has the same clinical efficacy as gemcitabine, but with less toxic and side effects than conventional drugs.
既往报道显示,S-1在晚期非小细胞肺癌(NSCLC)的维持治疗中具有显著疗效,且毒性和副作用低于传统药物。
探讨S-1维持治疗晚期NSCLC患者的疗效及安全性。
选取2015年9月至2018年4月我院收治的94例NSCLC患者纳入研究,采用随机数字表法分为S-1组(47例)和吉西他滨组(47例)。S-1组采用S-1治疗,吉西他滨组接受吉西他滨治疗。评估两组患者治疗后的临床疗效及生活质量。
两组总有效率比较差异无统计学意义( = 0.519)。生活质量评分显示,两组在GQOLI-74问卷的四个维度上差异均无统计学意义( = 0.518、0.094、0.338、0.418)。S-1组恶心呕吐、粒细胞减少及腹泻的发生率显著低于吉西他滨组(分别为 = 0.001、0.001和0.001)。两组血小板减少发生率( = 0.366)、无进展生存期( = 0.064)及生存率比较差异均无统计学意义( = 0.050)。
S-1维持治疗晚期NSCLC患者疗效显著。其临床疗效与吉西他滨相当,但毒性和副作用低于传统药物。