首页> 外文期刊>Thoracic cancer. >First‐line pemetrexed/carboplatin or cisplatin/bevacizumab compared with paclitaxel/carboplatin/bevacizumab in patients with advanced non‐squamous non‐small cell lung cancer with wild‐type driver genes: A real‐world study in China
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First‐line pemetrexed/carboplatin or cisplatin/bevacizumab compared with paclitaxel/carboplatin/bevacizumab in patients with advanced non‐squamous non‐small cell lung cancer with wild‐type driver genes: A real‐world study in China

机译:与野生型驾驶基因的先进非鳞状非小细胞肺癌患者的紫杉醇/卡铂/贝伐单抗与野生型驾驶基因的患者相比,第一线磷酸盐/卡铂/贝伐肽:在中国的真实研究

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The study was conducted to compare the effectiveness and safety of pemetrexed/carboplatin or cisplatin/bevacizumab (PemPBev) and paclitaxel/carboplatin/bevacizumab (PacCBev) as first-line therapy for advanced non-squamous non-small cell lung cancer (NS-NSCLC) patients with wild-type driver genes in a real-world setting. We retrospectively collected the medical records of advanced NS-NSCLC patients with wild-type driver genes administered first-line PemPBev or PacCBev therapy at Shanghai Chest Hospital between January 2014 and June 2016, and analyzed the differences in survival outcomes, efficacy, and safety between PemPBev and PacCBev treatment. A total of 390 patients were included in our analysis: 249 in the PemPBev group and 141 in the PacCBev group. Patients administered PemPBev experienced significantly improved progression-free survival (PFS) and overall survival (OS) compared to those administered PacCBev (PFS 7.5 vs. 6.2?months, hazard ratio [HR] 0.66, 95% confidence interval [CI] 0.53-0.84, P ?0.001; OS:18.6 vs. 16.0?months, HR?0.68, 95% CI 0.52-0.90, P =?0.002). The objective response rate (ORR) and disease control rate (DCR) were similar between the groups (ORR 21.7% vs. 30.5%, P?=?0.053; DCR 69.1% vs. 67.4%, P =?0.728). There was no significant difference in the incidence of adverse events between the groups (64.7% vs. 68.8%; P =?0.407), but the incidence of peripheral neuropathy in the PacCBev group was higher than in the PemPBev group (7.8% vs. 2.4%; P =?0.012). Our study shows that for advanced NS-NSCLC patients with wild-type driver genes, first-line PemPBev might be a better treatment option compared to PacCBev. ? 2019 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd.
机译:进行该研究以比较磷酸盐/卡铂或顺铂/贝伐单抗(PEMPBEV)和紫杉醇/卡铂/贝伐单抗(PACCBEV)作为先进非鳞状非小细胞肺癌(NS-NSCLC)的一线治疗(NS-NSCLC)的有效性和安全性)伴有野生型驾驶员基因的患者在真实世界的环境中。我们回顾性地将先进的NS-NSCLC患者的医疗记录在2014年1月至2016年1月至2016年1月至2016年1月至2016年6月间在上海胸部医院管理的野生型驱动基因,并分析了生存结果,疗效和安全性的差异Pempbev和Paccbev治疗。我们的分析中共有390名患者:PEMPBEV集团中的249名和PACCBEV组中的141名。与施用的PACBEV(PFS 7.5对6.2〜6.2个月,危险比[HR] 0.66,95%置信区间[CI] 0.53-0.84,患者施用Pempbev的患者显着改善了无进展的存活(PFS)和总存活(OS)和总存活率(OS)。0.66,95%置信区间[CI] 0.53-0.84 ,p <0.001; OS:18.6与16.0?月,HR?0.68,95%CI 0.52-0.90,P = 0.002)。基团之间的客观反应率(ORR)和疾病控制率(DCR)相似(ORR 21.7%与30.5%,p≤0.053; DCR 69.1%与67.4%,P = 0.728)。这些群体之间不良事件发生率没有显着差异(64.7%与68.8%; p = 0.407),但PACCBEV组周围神经病变的发生率高于PEMPBEV组(7.8%对) 2.4%; p = 0.012)。我们的研究表明,对于野生型驾驶员基因的高级NS-NSCLC患者,与PACCBEV相比,一线Pempbev可能是一个更好的治疗选项。 ? 2019年的作者。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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