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Efficacy of gemcitabine plus platinum agents for biliary tract cancers: A meta-analysis

机译:吉西他滨联合铂类药物治疗胆道癌的疗效:荟萃分析

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The objective of this study was to carry out a meta-analysis of the efficacy of gemcitabine+platinum agent regimens in the treatment of advanced biliary tract cancer (BTC). PubMed and Google Scholar were searched using the following combination of search terms: gemcitabine, oxaliplatin, cholangiocarcinoma, biliary, gallbladder, bile duct. Studies were eligible for inclusion in the meta-analysis if they were randomized trials on the use of gemcitabine plus a platinum agent for the treatment of advanced (unresectable or metastatic cancer) BTC. Outcomes of interest were response rate, overall survival, and progression-free survival. Pooled odds ratios/differences in median survival and 95% confidence intervals (CIs) were determined for each outcome. A total of 47 records were identified in the initial search. Ultimately, three open-label randomized trials (two phase 2 and one phase 3) met the eligibility criteria and were included in the meta-analysis. Two studies compared gemcitabine plus cisplatin with gemcitabine alone, whereas the other study compared gemcitabine plus oxaliplatin with fluorouracil-folinic acid. The total number of patients in the studies ranged from 54 to 410. The overall analyses revealed that all survival outcomes assessed were significantly more favorable for patients treated with gemcitabine plus platinum agents than for patients not treated with this combination. Response rates: odds ratio=2.639, 95% CI=1.210-5.757, Z=2.439, P=0.015; pooled difference in median overall survival=3.822 months, 95% CI=1.798-5.845 months, Z=3.702, P<0.001; pooled difference in median progression-free survival=3.268 months, 95% CI=1.996-4.541 months, Z=5.035, P<0.001. Patients with advanced BTC who are treated with gemcitabine plus platinum agents may experience better survival outcomes compared with patients who are not treated with this combination of chemotherapy.
机译:这项研究的目的是对吉西他滨+铂类药物治疗晚期胆道癌(BTC)的疗效进行荟萃分析。使用以下搜索词组合搜索PubMed和Google Scholar:吉西他滨,奥沙利铂,胆管癌,胆道,胆囊,胆管。如果研究是关于使用吉西他滨加铂试剂治疗晚期(不可切除或转移性癌症)BTC的随机试验,则符合纳入荟萃分析的条件。感兴趣的结果是缓解率,总生存期和无进展生存期。确定每个结果的合并比值比/中位生存期和95%置信区间(CI)的差异。初步搜索共找到47条记录。最终,三项开放标签的随机试验(两个2期和一个3期)符合入选标准,并纳入荟萃分析。两项研究比较了吉西他滨加顺铂与单独的吉西他滨,而另一项研究比较了吉西他滨加奥沙利铂与氟尿嘧啶-亚叶酸。研究中的患者总数为54至410。总体分析表明,吉西他滨联合铂类药物治疗的患者的所有生存期评估结果均显着优于未联合使用吉西他滨的患者。回应率:比值比= 2.639,95%CI = 1.210-5.757,Z = 2.439,P = 0.015;中位总生存期合并差异= 3.822个月,95%CI = 1.798-5.845个月,Z = 3.702,P <0.001;中位无进展生存期合并差异= 3.268个月,95%CI = 1.996-4.541个月,Z = 5.035,P <0.001。与未接受这种化学疗法联合治疗的患者相比,接受吉西他滨加铂类药物治疗的晚期BTC患者的生存结局可能更好。

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