临床肿瘤学杂志

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替吉奥联合复方苦参注射液治疗老年晚期胃癌的疗效和安全性分析

朴瑛,郑振东,唐玲,谭林深,刘兆喆,章国晶,谢晓冬   

  1. 110840 沈阳 沈阳军区总医院全军肿瘤诊治中心肿瘤科
  • 收稿日期:2015-11-06 修回日期:2016-04-06 出版日期:2016-06-30 发布日期:2016-06-30
  • 通讯作者: 谢晓冬

Efficacy and safety of S-1 combined with compound kushen injection as first-line treatment in older patients with advanced gastric cancer

PIAO Ying, ZHENG Zhendong, TANG Ling, TAN Linshen, LIU Zhaozhe, ZHANG Guojing, XIE Xiaodong
  

  1. Department of Oncology, Oncology Diagnosis and Treatment Center, the General Hospital of Shenyang Military Region, Shenyang 110840,China
  • Received:2015-11-06 Revised:2016-04-06 Online:2016-06-30 Published:2016-06-30
  • Contact: XIE Xiaodong

摘要: 目的 探讨替吉奥(S-1)联合复方苦参注射液治疗老年晚期胃癌的疗效和安全性。
方法选取沈阳军区总医院肿瘤科收治的70岁以上老年胃癌患者63例,剔除中途因疾病进展而中止治疗及脱落的4例患者,共59例入组,按随机数字表法分为对照组(n=28)和联合组(n=31),对照组口服单药S-1(40 mg/m2,2次/日),联合组在其基础上联合复方苦参注射液(20 ml,d1~d14),两组均28天为1个周期。评价两组的疗效、不良反应并随访生存情况。结果联合组总有效率(RR)和疾病控制率(DCR)分别为54.9%和90.3%,对照组的RR和DCR分别为393%和857%,差异无统计学意义(P>0.05);两组的不良反应多为1~2级,其中联合组乏力、肝功损伤发生率分别为83.9%、74.2%,低于对照组的100.0%、96.4%,差异有统计学意义(P<0.05);联合组的中位无进展生存期为9.0个月,长于对照组的 7.9个月,差异有统计学意义(P<0.05);两组中位总生存期分别为14.6个月和13.1个月,差异无统计学意义(P>0.05)。结论S-1联合复方苦参注射液可延长老年晚期胃癌患者的无进展生存期,且不良反应轻微,安全性较高,值得临床推广。

Abstract: Objective To explore the effecacy and safety of S-1 plus compound kushen injection curative treatment for advanced gastric cancer. Methods Sixty-three elderly patients over the age of 70 with gastric cancer from the general hospital of shenyang military region were enrolled,excluding 4 patients of disease progression and fall off. Fifty-nine patients in total according to random number table method were divided into 28 cases as the control group and 31 cases as combined group. The control group was taken S-1 orally(40 mg/m2), and combined group was taken S-1 plus compound kushen injection. The effecacy,adverse reactions and survival were observed. Results The response rate(RR)and disease control rate(DCR) of combined group were 549% and 903%, which were similar with 39.3% and 85.7% of the control group(P>0.05). The main side effects were of grade 1-2 in both groups. The incidence of weakness and hepatic injury in combined group were 83.9% and 74.2%, lower than those in control group(100.0% and 96.4%), respectively(P<0.05). The median progression-free survival of combined group was 9.0 months, higher than 7.9 months in control group(P<0.05). The median overall survival in combined group and control group was 14.6 months and 13.1 months(P>0.05). ConclusionS-1 combined with compound kushen injection for the treatment of elderly advanced gastric cancer has a longer progression-free survival with slight adverse reactions,worthy of clinical promotion.

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