Winship Cancer Institute of Emory University, Atlanta, GA.
Dana-Farber Cancer Institute, Boston, MA.
J Clin Oncol. 2019 Sep 10;37(26):2360-2367. doi: 10.1200/JCO.19.01006. Epub 2019 Jul 30.
Pemetrexed or bevacizumab is used for maintenance therapy of advanced nonsquamous non-small-cell lung cancer (NSCLC). The combination of bevacizumab and pemetrexed has also demonstrated efficacy. We conducted a randomized study to determine the optimal maintenance therapy.
Patients with advanced nonsquamous NSCLC and no prior systemic therapy received carboplatin (area under the curve, 6), paclitaxel (200 mg/m), and bevacizumab (15 mg/kg) for up to four cycles. Patients without progression after four cycles were randomly assigned to maintenance therapy with bevacizumab (15 mg/kg), pemetrexed (500 mg/m), or a combination of the two agents. The primary end point was overall survival, with bevacizumab serving as the control group.
Of the 1,516 patients enrolled, 874 (57%) were randomly assigned after induction therapy to one of the three maintenance therapy groups. With a median follow-up of 50.6 months, median survival with pemetrexed was 15.9 months, compared with 14.4 months with bevacizumab (hazard ratio [HR], 0.86; = .12); median survival with pemetrexed and bevacizumab was 16.4 months (HR, 0.9; = .28); median progression-free survival was 4.2, 5.1 (HR, 0.85; = .06), and 7.5 months (HR, 0.67; < .001) for the three groups, respectively. Incidence of worst grade 3 to 4 toxicity was 29%, 37%, and 51%, respectively, for bevacizumab, pemetrexed, and the combination regimen.
Single-agent bevacizumab or pemetrexed is efficacious as maintenance therapy for advanced nonsquamous NSCLC. Because of a lack of survival benefit and higher toxicity, the combination of bevacizumab and pemetrexed cannot be recommended.
培美曲塞或贝伐珠单抗用于晚期非鳞状非小细胞肺癌(NSCLC)的维持治疗。贝伐珠单抗联合培美曲塞也显示出疗效。我们进行了一项随机研究,以确定最佳的维持治疗方案。
无既往全身治疗的晚期非鳞状 NSCLC 患者接受卡铂(曲线下面积 6)、紫杉醇(200mg/m)和贝伐珠单抗(15mg/kg)治疗,最多四个周期。四个周期后无进展的患者随机分配至贝伐珠单抗(15mg/kg)、培美曲塞(500mg/m)或两者联合的维持治疗组。主要终点是总生存期,以贝伐珠单抗作为对照组。
在纳入的 1516 名患者中,874 名(57%)在诱导治疗后随机分配至三个维持治疗组中的一个组。中位随访 50.6 个月时,培美曲塞组的中位生存期为 15.9 个月,贝伐珠单抗组为 14.4 个月(风险比[HR],0.86;P=.12);培美曲塞联合贝伐珠单抗组的中位生存期为 16.4 个月(HR,0.9;P=.28);三组的中位无进展生存期分别为 4.2、5.1(HR,0.85;P=.06)和 7.5 个月(HR,0.67;P<.001)。贝伐珠单抗、培美曲塞和联合方案组的 3 至 4 级最严重毒性发生率分别为 29%、37%和 51%。
单药贝伐珠单抗或培美曲塞作为晚期非鳞状 NSCLC 的维持治疗是有效的。由于缺乏生存获益和更高的毒性,不推荐贝伐珠单抗和培美曲塞联合治疗。