Translational Medicine Research Center, Shanxi Medical University, Taiyuan, PR China.
Department of Pathology & Shanxi Key Laboratory of Carcinogenesis and Translational Research on Esophageal Cancer, Shanxi Medical University, Taiyuan, PR China.
Int J Clin Pract. 2020 Jul;74(7):e13510. doi: 10.1111/ijcp.13510. Epub 2020 Apr 29.
Gemcitabine has been proved to be effective in many advanced cancer. However, almost all trials failed to demonstrate the response rate of gemcitabine-based combination schedules on oesophageal cancer (EC).
A systematic meta-analysis of randomised clinical trials (RCTs) was performed to investigate the efficacy of gemcitabine-based combination chemotherapy in EC treatment. Clinical trials were collected during the period ranging from January 2000 to November 2018 by searching different databases. Odds-ratios (ORs) of response rate (RR), disease control rate (DCR) and grade 3-4 toxicity rates (TRs) were extracted as presented in retrieved studies.
Fourteen trials (1024 patients) were selected for the final analysis. The results showed that RR and DCR of gemcitabine-based combination chemotherapy demonstrated a significant advantage for non-gemcitabine therapy (OR for RR: 1.51; 95% CI: 1.16-1.96; P = .002; OR for DCR: 1.66; 95% CI: 1.19-2.32, P = .003). Toxicities of gemcitabine-based combination chemotherapy on gastrointestinal tract (OR, 0.39; 95% CI: 0.24-0.63, P = .0001) were less frequent compared to that of the non-gemcitabine therapy.
The improvements of gemcitabine-based combination chemotherapy on RR, CDR and reduction of gastrointestinal tract, hepatic and renal for EC patients suggests that the combined chemotherapy based on gemcitabine could be a potential treatment options for advanced EC.
吉西他滨已被证明在许多晚期癌症中有效。然而,几乎所有的试验都未能证明吉西他滨为基础的联合方案在食管癌(EC)中的反应率。
系统地对随机临床试验(RCTs)进行了荟萃分析,以研究吉西他滨为基础的联合化疗在 EC 治疗中的疗效。通过检索不同的数据库,收集了 2000 年 1 月至 2018 年 11 月期间的临床试验。从检索到的研究中提取了反应率(RR)、疾病控制率(DCR)和 3-4 级毒性发生率(TRs)的优势比(ORs)。
最终有 14 项试验(1024 例患者)被纳入最终分析。结果表明,吉西他滨为基础的联合化疗的 RR 和 DCR 对非吉西他滨治疗具有显著优势(RR 的 OR:1.51;95%CI:1.16-1.96;P=0.002;DCR 的 OR:1.66;95%CI:1.19-2.32,P=0.003)。与非吉西他滨治疗相比,吉西他滨为基础的联合化疗对胃肠道的毒性较小(OR,0.39;95%CI:0.24-0.63,P=0.0001)。
吉西他滨为基础的联合化疗对 RR、CDR 的改善以及胃肠道、肝和肾毒性的降低,提示吉西他滨为基础的联合化疗可能是晚期 EC 的一种潜在治疗选择。