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Feasibility and effectiveness of afatinib for poor performance status patients with EGFR-mutation-positive non-small-cell lung cancer: a retrospective cohort study

机译:AFATINIB适用于贫困性状态患者EGFR-突变阳性非小细胞肺癌的可行性和有效性:回顾性队列研究

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Afatinib is one of the standard treatments for patients with epidermal growth factor receptor (EGFR)-mutated non-small-cell lung cancer (NSCLC). However, data on the use of afatinib in patients with poor performance status (PS?≥?2) are limited. This study aimed to retrospectively review the clinical outcomes and safety of afatinib treatment in EGFR-mutation-positive (EGFRm ) NSCLC patients with PS?≥?2. The data for 62 patients who were treated at Linkou Chang Gung Memorial Hospital from January 2010 to August 2019 were retrospectively reviewed. Patients’ clinicopathological features were obtained, and univariate and multivariate analyses were performed to identify possible prognostic factors. Data on adverse events were collected to evaluate general tolerance for afatinib therapy. Until February 2020, the objective response rate, disease control rate, median progression-free survival (PFS), and overall survival (OS) were 58.1% (36/62), 69.4% (43/62), 8.8?months, and 12.9?months, respectively. The absence of liver metastasis (PFS: p?=?0.044; OS: p?=?0.061) and good disease control (p??0.001 for PFS and OS) were independent favorable prognostic factors for PFS and OS. Bone metastasis (p?=?0.036) and dose modification (reduction/interruption, p?=?0.021) were predictors of disease control. Afatinib demonstrated acceptable efficacy and safety in the current cohort. This study provided evidence to support the use of afatinib as a first-line treatment in EGFRm NSCLC patients with poor PS.
机译:AFATINIB是表皮生长因子受体(EGFR)审查的非小细胞肺癌(NSCLC)患者的标准治疗之一。但是,有关使用性能差的患者使用AFATINIB(PS?≥?2)的数据有限。本研究旨在回顾性质审查EGFR-突变阳性(EGFRM)NSCLC患者的AFATINIB治疗的临床结果和安全性PS?≥?2。回顾性审查了2010年1月至2019年8月在2010年1月至2019年8月对待的62例患者的数据。获得患者的临床病理学特征,进行单变量和多变量分析以确定可能的预后因素。收集有关不良事件的数据,以评估Afatinib疗法的一般耐受性。直到2020年2月,客观反应率,疾病控制率,无进展的不良生存(PFS)和总体存活(OS)为58.1%(36/62),69.4%(43/62),8.8?月,和12.9?几个月。没有肝脏转移(PFS:P?= 0.044; OS:P?= 0.061)和良好的疾病对照(P?PFS和OS的PFS和OS)是PFS和OS的独立良好的预后因素。骨转移(p?= 0.036)和剂量修饰(减少/中断,p?= 0.021)是疾病控制的预测因子。 Afatinib在当前队列中显示出可接受的疗效和安全性。本研究提供了证据,以支持使用AFATINIB作为EGFRM NSCLC患者贫困PS患者的一线治疗。

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