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Efficacy and safety of gemcitabine plus erlotinib for locally advanced or metastatic pancreatic cancer: a systematic review and meta-analysis

机译:吉西他滨联合厄洛替尼治疗局部晚期或转移性胰腺癌的疗效和安全性:系统评价和荟萃分析

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Background: Pancreatic cancer is considered as a chemoresistant neoplasm with extremely dismal prognosis. Gemcitabine is recommended as the standard agent for locally advanced or metastatic pancreatic cancer. A series of trials have been conducted to improve the outcome of advanced pancreatic cancer with other anticancer drugs in combination with gemcitabine. Unfortunately, the designers of the clinical trials failed to improve the poor prognosis of patients with advanced pancreatic cancer. Erlotinib was the first additional drug that improved the overall survival of patients with advanced pancreatic cancer with gemcitabine. We performed this systematic review and meta-analysis to explore the efficacy and safety of the combination of gemcitabine with erlotinib (GemErlo) for patients with advanced pancreatic cancer using the currently available evidence. Methods: PubMed/MEDLINE, EMBASE, the Cochrane Library, and relevant abstracts of major conferences were comprehensively searched. Data results on objective response rate, disease control rate, and 1-year survival were pooled by using MetaAnalyst with a random-effects model. Results on progression-free survival and overall survival were only summarized descriptively. Results: A total of 24 studies with 1,742 patients with locally advanced or metastatic pancreatic cancer treated with GemErlo were included. Combined objective response rate was 14.4% (95% CI:?11.6%–17.7%), disease control rate was 55.0% (95% CI: 51.5%–58.5%), and 1-year survival rate was 28.5% (95% CI: 24.0%–33.4%). Progression-free survival ranged from 2.63 to 9.6 months, and overall survival varied from 6?to?10?months. As for the toxicity profile, the most common adverse events (AEs) were hematologic reactions, skin rash, and gastrointestinal reactions. Other severe AEs, which had low incidence, included treatment-induced death and interstitial lung disease. Conclusion: Our study showed that GemErlo is associated with reasonable activity in treating patients with locally advanced or metastatic pancreatic cancer. Most of the AEs were tolerable, while some severe AEs needed careful detection.
机译:背景:胰腺癌被认为是一种化学耐药性肿瘤,预后极差。建议吉西他滨作为局部晚期或转移性胰腺癌的标准药物。已经进行了一系列试验,以与其他抗癌药物联合吉西他滨改善晚期胰腺癌的预后。不幸的是,临床试验的设计者未能改善晚期胰腺癌患者的不良预后。厄洛替尼是吉西他滨可改善晚期胰腺癌患者总体生存率的首个额外药物。我们进行了这项系统的综述和荟萃分析,以吉西他滨联合厄洛替尼(GemErlo)对晚期胰腺癌患者的有效性和安全性进行研究。方法:全面检索PubMed / MEDLINE,EMBASE,Cochrane图书馆以及主要会议的相关摘要。使用具有随机效应模型的MetaAnalyst收集关于客观缓解率,疾病控制率和1年生存率的数据结果。无进展生存期和总体生存期的结果仅是描述性的。结果:共纳入24项研究,研究1,742例接受GemErlo治疗的局部晚期或转移性胰腺癌患者。综合客观缓解率为14.4%(95%CI:?11.6%–17.7%),疾病控制率为55.0%(95%CI:51.5%–58.5%),一年生存率为28.5%(95%) CI:24.0%–33.4%)。无进展生存期为2.63到9.6个月,总生存期为6到10个月。至于毒性,最常见的不良事件是血液学反应,皮疹和胃肠道反应。其他严重的不良事件发生率低,包括治疗引起的死亡和间质性肺疾病。结论:我们的研究表明,GemErlo在治疗局部晚期或转移性胰腺癌患者中具有合理的活性。大多数不良事件是可以忍受的,而一些严重不良事件需要仔细检测。

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