文章摘要
张莹莹,李娜苗,范亚莉,赵瑞婧,王丽娜,李建英.广泛期小细胞肺癌中顺铂联合伊立替康与顺铂联合依托泊苷的Meta分析[J].实用中西医结合临床,2019,19(3):
广泛期小细胞肺癌中顺铂联合伊立替康与顺铂联合依托泊苷的Meta分析
A meta analysis of Cisplatin combined with irinotecan and cisplatin combined etoposide in the first-line treatment for extensive stage small cell lung cancer
投稿时间:2018-10-27  修订日期:2018-12-29
DOI:
中文关键词: 小细胞肺癌  伊立替康  依托泊苷  Meta分析
英文关键词: Small-cell lung cancer  irinotecan  etoposide  Meta analysis
基金项目:陕西省中医管理局中医药科研课题任务书/西安市科技计划项目
作者单位E-mail
张莹莹 陕西省西安市中心医院呼吸科 1210918274@qq.com 
李娜苗 陕西省西安市中心医院呼吸科  
范亚莉 陕西省西安市中心医院呼吸科  
赵瑞婧 陕西省西安市中心医院呼吸科  
王丽娜 陕西省西安市中心医院呼吸科  
李建英* 陕西省西安市中心医院呼吸科 380694564@qq.com 
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中文摘要:
      目的 评价顺铂联合伊立替康与顺铂联合依托泊苷治疗广泛期小细胞肺癌的临床疗效及安全性。方法:计算机检索Pubmed、Medline、中国知网(CNKI)、维普网(VIP)及万方数据知识服务平台等数据库,筛选关于顺铂联合伊立替康(IP)与顺铂联合依托泊苷(EP)治疗广泛期小细胞肺癌的相关文献,检索时间为建库至2018年8月。实验组患者采用顺铂联合伊立替康,对照组患者采用顺铂联合依托泊苷;采用RevMan 5.3.0软件进行Meta分析。结果 最终纳入8篇文献,均为中文文献,包括488例患者,IP组与EP组临床有效率(RR)(OR=1.06,95%CI:0.93~1.21,P=0.41)、疾病控制率(DCR)(OR=1.02,95%CI:0.91~1.13,P=0.77)方面上差异无统计学意义。在安全性方面,IP主要表现为消化道毒性(OR=3.8,95%CI:2.39~6.02,P<0.00001),EP主要表现为血液毒性,特别是中性粒细胞减少(OR=0.45,95%CI:0.29~0.70,P=0.0004)。结论 IP方案的疗效与EP方案相似,对小细胞癌有较好的临床应用价值。IP方案毒性主要表现在消化系统,EP方案毒性主要表现在骨髓抑制。
英文摘要:
      Objective To assess the efficacy and safety of etoposide combined with irinotecan and cisplatin regimens in patients with extensive small cell lung cancer.Methods we searched Pubmed,Medline,CNKI,VIP and WanFang Data to collect the literature on cisplatin combined with irinotecan (IP) and cisplatin combined with etoposide (EP) in the treatment of extensive small cell lung cancer from creating database to August 2018. The experimental group was treated with cisplatin combined with irinotecan, the control group with cisplatin combined with etoposide, and the RevMan 5.3.0 software was used for meta-analysis.Results There was no significant difference in clinical efficacy (RR) (OR = 1.06, 95% CI: 0.93-1.21, P = 0.41), disease control rate (DCR) (OR = 1.02, 95% CI: 0.91-1.13, P = 0.77) between IP group and EP group. In terms of safety, IP was mainly gastrointestinal toxicity (OR = 3.8, 95% CI: 2.39-6.02, P < 0.00001), EP was mainly hematotoxicity, especially neutropenia (OR = 0.45, 95% CI: 0.29-0.70, P = 0.0004). Conclusion The efficacy of IP is similar to EP, and it has better clinical application value for small cell carcinoma. IP toxicity was mainly manifested in the digestive system, EP toxicity was mainly manifested in bone marrow suppression.
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