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Primary tumor resection of non‐small cell lung cancer patients with ipsilateral pleural dissemination (M1a) in the era of targeted therapy

机译:在靶向治疗时代的同侧胸膜肺癌(M1A)中非小细胞肺癌患者的原发性肿瘤切除

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BACKGROUND:Non-small cell lung cancer (NSCLC) patients with ipsilateral pleural dissemination (M1a) are generally contraindicated for surgery. Recently, several studies have demonstrated that these patients might benefit from primary tumor resection (PTR). However, whether PTR is beneficial for driver oncogene-positive patients treated with targeted therapy, remains unclear. Here, we investigated the effects of PTR on survival in the era of targeted therapy.METHODS:In total, 105 NSCLC patients with ipsilateral pleural dissemination were identified. The mode of systemic treatment was assessed in this study. Survival analysis was performed with the Kaplan-Meier method and Cox proportional hazards regression. The overall survival (OS) of patients with or without PTR was compared between propensity score-matched groups (caliper: 0.02).RESULTS:In the entire cohort, PTR was associated with improved OS in both unmatched (median survival time [MST]: 50.0 vs. 29.6?months, P = 0.019) and matched (MST: 50.0 vs. 34.4?months, P = 0.052) cohorts. Multivariate regression models showed that surgery was an independent favorable prognostic factor for OS. A total of 70 patients underwent genetic testing, and targeted therapies, such as EGFR-TKIs or ALK-TKIs, were used in the driver oncogene-positive patients. Subgroup analysis showed that PTR did not improve OS in the targeted therapy group (MST: 57.1 months vs. 50.4?months, P = 0.840). However, surgery significantly prolonged survival in the nontargeted therapy group (MST: 39.8 vs. 14.2?months, P = 0.002).CONCLUSIONS:The results of this study indicated that PTR could prolong OS in stage IV NSCLC patients with ipsilateral pleural dissemination, especially in patients who are not candidates for targeted therapy.KEY POINTS:Non-small cell lung cancer patients with ipsilateral pleural dissemination can benefit from primary tumor resection. Primary tumor resection could prolong overall survival (OS) in non-small cell lung cancer patients with ipsilateral pleural dissemination who are not candidates for targeted therapy.? 2020 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd.
机译:背景:非小细胞肺癌(NSCLC)具有同侧胸膜渗透(M1A)的患者通常对手术进行禁用。最近,一些研究表明,这些患者可能受益于原发性肿瘤切除(PTR)。但是,PTR是否有利于司机癌基因阳性患者治疗靶向治疗,仍然不清楚。在这里,我们研究了PTR在靶向治疗时代的生存中的影响。方法:鉴定了105例Ipsilidal胸膜渗透患者。在本研究中评估了全身治疗模式。通过Kaplan-Meier方法和Cox比例危害回归进行存活分析。在倾向分数匹配组之间比较有或没有PTR患者的整体存活(OS)(CALIPER:0.02)。结果:在整个队列中,PTR在无与伦比的(中位生存时间[MST]中有改善的操作系统相关联: 50.0与29.6?月,P = 0.019)和匹配(MST:50.0与34.4?月,P = 0.052)队列。多元回归模型显示,手术是OS的独立良好的预后因素。在司机癌阳性阳性患者中使用总共70名患者接受遗传检测和靶向疗法,例如EGFR-TKIS或ALK-TKIS。亚组分析表明,PTR在靶向治疗组中没有改善OS(MST:57.1个月与50.4个月,P = 0.840)。然而,手术在不准确的治疗组中显着延长存活(MST:39.8与14.2?月份,P = 0.002)。结论:本研究的结果表明,PTR可以在IV阶段NSCLC患者中延长OV的同侧胸膜传播患者。在没有针对性治疗的候选人的患者中.KEY点:非小细胞肺癌患者患有同侧胸膜肺化患者​​可以从原发性肿瘤切除中受益。原发性肿瘤切除术可以延长非小细胞肺癌患者的总生存期(OS)患有同侧胸膜传播的患者,该胸膜传播不是针对靶向治疗的候选者。 2020作者。中国肺部肿瘤集团和约翰瓦里和儿子澳大利亚发表的胸癌

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