Pulmonary Department, Shanghai Chest Hospital, Shanghai Jiao Tong University, Shanghai, China.
Thorac Cancer. 2019 May;10(5):1043-1050. doi: 10.1111/1759-7714.13025. Epub 2019 Mar 22.
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.
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。
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。
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)。
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。