Medical Oncology, Santa Maria della Misericordia Hospital, via Dottori 1, 06156 Perugia, Italy.
Section of Anatomic Pathology and Histology, Department of Medicine and Surgery, University of Perugia, Piazza Lucio Severi 1, 06132 Perugia, Italy.
Genes (Basel). 2021 Apr 30;12(5):679. doi: 10.3390/genes12050679.
Besides platinum-based chemotherapy, no established treatment option exists for advanced non-small-cell lung cancer (NSCLC) patients with exon 20 (Ex20ins) insertion mutations. We sought to determine the clinical outcome of patients with this mutation subtype in the immunotherapy era. Thirty NSCLCs with Ex20ins mutations were identified, of whom 15 had received immune checkpoint blockade (ICB) treatment as monotherapy (N = 12), in combination with chemotherapy (N = 2) or with another immunotherapeutic agent (N = 1). The response rate was observed in 1 out of 15 patients (6.7%), median progression-free survival (PFS) was 2.0 months and median overall survival (OS) was 5.3 months. A trend towards an inferior outcome in terms of PFS and OS was observed for patients receiving ICB treatment in the first versus second line setting (PFS: 1.6 months versus 2.7 months, respectively, = 0.16-OS: 2.0 months versus 8.1 months, respectively, = 0.09). Median OS from the time of diagnosis of advanced disease was shorter for patients treated with ICB versus those who did not receive immunotherapy (12.9 months versus 25.2 months, respectively, = 0.08), which difference remained associated with a worse survival outcome at multivariate analysis ( = 0.04). Treatment with ICB is poorly effective in NSCLCs with Ex20ins mutations, especially when given in the first-line setting. This information is crucial in order to select the optimal treatment strategy for patients with this subtype of mutation.
除了基于铂类的化疗,对于存在外显子 20(Ex20ins)插入突变的晚期非小细胞肺癌(NSCLC)患者,没有既定的治疗选择。我们试图确定免疫治疗时代该突变亚型患者的临床结局。鉴定出 30 例存在 Ex20ins 突变的 NSCLC,其中 15 例接受了免疫检查点阻断(ICB)单药治疗(N=12),联合化疗(N=2)或另一种免疫治疗药物(N=1)。15 例患者中有 1 例(6.7%)观察到缓解率,中位无进展生存期(PFS)为 2.0 个月,中位总生存期(OS)为 5.3 个月。接受 ICB 一线与二线治疗的患者,PFS(1.6 个月与 2.7 个月,=0.16-OS:2.0 个月与 8.1 个月,=0.09)和 OS 均呈下降趋势。与未接受免疫治疗的患者相比,接受 ICB 治疗的患者从晚期疾病诊断开始的 OS 更短(12.9 个月与 25.2 个月,=0.08),在多变量分析中,这种差异与生存结局更差仍相关(=0.04)。ICB 治疗在 Ex20ins 突变的 NSCLC 中效果不佳,特别是在一线治疗中。这一信息对于选择该突变亚型患者的最佳治疗策略至关重要。