首页> 外文期刊>Journal of Thoracic Disease >Non-significant efficacy of icotinib plus pleurodesis in epidermal growth factor receptor positive mutant lung cancer patients after malignant pleural effusion drainage compared to icotinib alone
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Non-significant efficacy of icotinib plus pleurodesis in epidermal growth factor receptor positive mutant lung cancer patients after malignant pleural effusion drainage compared to icotinib alone

机译:icotinib加上表皮生长因子受体阳性突变体肺癌患者的非显着疗效与单独的icotinib相比恶性胸腔积液引流后

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Background: To investigate the efficacy and safety of icotinib plus pleurodesis or icotinib alone in epidermal growth factor receptor (EGFR) positive mutant lung cancer patients after malignant pleural effusion (MPE) drainage. Methods: In this retrospective study from initially reviewed case reports of 230 lung adenocarcinoma patients with MPE who were EGFR mutation positive and treated in our hospital between Jan 2014 and Dec 2016 consecutively, 51 patients who met the inclusion criteria were divided into treated with oral icotinib plus pleurodesis and without pleurodesis after pleural effusion drainage groups. Case records including patient gender, age, smoking status and local treatments, as well as adverse events were collected and retrospectively analyzed. The clinical outcomes which were measured by progression free survival (PFS), objective response rate (ORR) & adverse reactions were analyzed by a Kaplan-Meier curve and a log-rank test after follow-ups. Results: The median PFS of patients who received icotinib plus pleurodesis was 8.4 months, while the median PFS of icotinib alone patients was 9.0 months (P=0.996, χ2=7.241). Similarly, the ORR for MPEs, with or without pleurodesis were not significantly difference (64.29% vs. 67.57%, P=0.824, χ2=0.049). Adverse reactions of pleurodesis were mainly fever, chest pain, gastrointestinal reactions and myelosuppression. Conclusions: Our results suggested that pleurodesis after MPE drainage had no difference on outcomes of icotinib therapy patients. However, pleurodesis may increase some adverse reactions, which might be inconvenient for patients in clinical practice.
机译:背景:研究恶性胸腔积液(MPE)引流后,探讨ICOTINIB PLUS PLELURODEASIC或ICOTINIB在表皮生长因子受体(EGFR)正突变体肺癌患者中的疗效和安全性。方法:在2014年1月至2016年1月至2016年1月在我们的医院中均为EGFR突变的MPE患者的初期审查的案例报告,从2014年1月至2016年12月,符合纳入标准的51名符合纳入标准的51名患者加上胸膜瘤和胸腔积液引流组后没有胸膜炎。收集和回顾性地分析了包括患者性别,年龄,吸烟状态和当地治疗的案例记录,以及不良事件。通过逐步存活(PFS),客观反应率(ORR)和不良反应测量的临床结果是通过KAPLAN-MEIER曲线分析和后续后的对数级试验。结果:接受icotinib加胸膜瘤的患者的中位数PFS为8.4个月,而单独患者的icotinib中位数为9.0个月(p = 0.996,χ2= 7.241)。类似地,用于MPE的ORR,有或没有胸膜炎的差异没有显着差异(64.29%对67.57%,P = 0.824,χ2= 0.049)。胸膜炎的不良反应主要是发热,胸痛,胃肠道反应和髓抑制。结论:我们的结果表明,MPE引流后的血液缺乏对icotinib治疗患者的结果没有差异。然而,胸膜炎可能会增加一些不良反应,这对于临床实践中的患者可能是不方便的。

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