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一线培美曲塞/卡铂或顺铂/贝伐珠单抗与紫杉醇/卡铂/贝伐珠单抗在野生型驱动基因晚期非鳞状非小细胞肺癌患者中的比较:中国真实世界研究。

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.

机构信息

Pulmonary Department, Shanghai Chest Hospital, Shanghai Jiao Tong University, Shanghai, China.

出版信息

Thorac Cancer. 2019 May;10(5):1043-1050. doi: 10.1111/1759-7714.13025. Epub 2019 Mar 22.

Abstract

BACKGROUND

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.

METHODS

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.

RESULTS

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).

CONCLUSION

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.

摘要

背景

本研究旨在比较培美曲塞/卡铂或顺铂/贝伐珠单抗(PemPBev)与紫杉醇/卡铂/贝伐珠单抗(PacCBev)作为野生型驱动基因晚期非鳞状非小细胞肺癌(NS-NSCLC)患者一线治疗的有效性和安全性,该研究在真实环境中进行。

方法

我们回顾性收集了 2014 年 1 月至 2016 年 6 月期间在上海胸科医院接受一线培美曲塞/卡铂或紫杉醇/卡铂/贝伐珠单抗治疗的晚期 NS-NSCLC 患者的病历,并分析了培美曲塞/卡铂/贝伐珠单抗与紫杉醇/卡铂/贝伐珠单抗治疗的生存结果、疗效和安全性差异。

结果

共纳入 390 例患者,其中培美曲塞/卡铂/贝伐珠单抗组 249 例,紫杉醇/卡铂/贝伐珠单抗组 141 例。与紫杉醇/卡铂/贝伐珠单抗组相比,培美曲塞/卡铂/贝伐珠单抗组患者的无进展生存期(PFS)和总生存期(OS)显著改善(PFS:7.5 个月 vs. 6.2 个月,风险比 [HR]0.66,95%置信区间 [CI]0.53-0.84,P < 0.001;OS:18.6 个月 vs. 16.0 个月,HR 0.68,95%CI 0.52-0.90,P = 0.002)。两组的客观缓解率(ORR)和疾病控制率(DCR)相似(ORR:21.7% vs. 30.5%,P = 0.053;DCR:69.1% vs. 67.4%,P = 0.728)。两组不良反应发生率无显著差异(64.7% vs. 68.8%,P = 0.407),但紫杉醇/卡铂/贝伐珠单抗组周围神经病变发生率高于培美曲塞/卡铂/贝伐珠单抗组(7.8% vs. 2.4%,P = 0.012)。

结论

本研究表明,对于野生型驱动基因晚期 NS-NSCLC 患者,一线培美曲塞/卡铂/贝伐珠单抗可能优于紫杉醇/卡铂/贝伐珠单抗。

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