Chen Jing, Pan Yin, Zhang Baishen, Li Meichen, Yu Hui, Yu Mingjie, Chen Likun
Department of Medical Oncology, Sun Yat-Sen University Cancer Center, State Key Laboratory of Oncology in South China; Guangdong Provincial Clinical Research Center for Cancer, Guangzhou, China.
Sun Yat-Sen University Cancer Center, State Key Laboratory of Oncology in South China; Guangdong Provincial Clinical Research Center for Cancer, Guangzhou, China.
Cancer Sci. 2025 Aug 15. doi: 10.1111/cas.70175.
Compared to exon 19 deletions, the epidermal growth factor receptor (EGFR) exon 21 L858R (21L858R) mutation is associated with a poorer prognosis in non-small cell lung cancer (NSCLC), particularly in patients with brain metastases (BMs). However, there is a notable lack of prospective or retrospective clinical studies focusing on this specific population. This study aims to evaluate the efficacy of different first-line treatment strategies using EGFR-tyrosine kinase inhibitors (TKIs) in NSCLC patients harboring the 21L858R mutation and BMs while providing insights into concurrent mutations and resistance mechanisms. We analyzed clinical data from 331 patients diagnosed with the EGFR 21L858R mutation and BMs who received first-line EGFR-TKI treatment at Sun Yat-sen University Cancer Center between April 2014 and June 2023 (ID: GASTO-1027). The efficacy was evaluated through intracranial progression-free survival (iPFS), PFS, and overall survival (OS). Compared to the first-generation and second-generation cohorts, the third-generation EGFR-TKI cohort demonstrated significant improvements in iPFS (p = 0.002), PFS (p < 0.001), and OS (p = 0.016). Within the third-generation EGFR-TKI group, the combination chemotherapy cohort exhibited the most favorable outcomes, with marked extensions in both iPFS (p = 0.037) and PFS (p = 0.049). Multivariate analyses identified the treatment regimen of third-generation TKIs combined with chemotherapy as an independent prognostic factor for improved iPFS. Compared to treatment regimens containing first-generation or second-generation EGFR-TKIs, patients with TP53 mutations derived greater benefit from treatment regimens containing third-generation EGFR-TKIs. The combination of third-generation EGFR-TKIs with chemotherapy shows enhanced efficacy in patients with EGFR 21L858R mutations and BMs compared to other treatments. Future prospective clinical trials are essential to assess this combination's effects in this population.
与外显子19缺失相比,表皮生长因子受体(EGFR)外显子21 L858R(21L858R)突变与非小细胞肺癌(NSCLC)患者预后较差相关,尤其是在有脑转移(BMs)的患者中。然而,显著缺乏针对这一特定人群的前瞻性或回顾性临床研究。本研究旨在评估使用EGFR酪氨酸激酶抑制剂(TKIs)的不同一线治疗策略对携带21L858R突变和BMs的NSCLC患者的疗效,同时深入了解并发突变和耐药机制。我们分析了2014年4月至2023年6月期间在中山大学肿瘤防治中心接受一线EGFR-TKI治疗的331例诊断为EGFR 21L858R突变和BMs患者的临床数据(ID:GASTO-1027)。通过颅内无进展生存期(iPFS)、无进展生存期(PFS)和总生存期(OS)评估疗效。与第一代和第二代队列相比,第三代EGFR-TKI队列在iPFS(p = 0.002)、PFS(p < 0.001)和OS(p = 0.016)方面有显著改善。在第三代EGFR-TKI组中,联合化疗队列表现出最有利的结果,iPFS(p = 0.037)和PFS(p = 0.049)均有显著延长。多变量分析确定第三代TKIs联合化疗的治疗方案是改善iPFS的独立预后因素。与包含第一代或第二代EGFR-TKIs的治疗方案相比,TP53突变患者从包含第三代EGFR-TKIs的治疗方案中获益更大。与其他治疗相比,第三代EGFR-TKIs与化疗联合在携带EGFR 21L858R突变和BMs的患者中显示出更高的疗效。未来的前瞻性临床试验对于评估这种联合治疗在该人群中的效果至关重要。