Gu Linping, Huang Huayan, Xu Zhangwendi, Niu Xiaomin, Li Ziming, Xia Liliang, Yu Yongfeng, Lu Shun
Department of Shanghai Lung Cancer Center, Shanghai Chest Hospital, School of Medicine, Shanghai Jiao Tong University, 241 Huaihai West Road, Shanghai 200030, China.
J Clin Med. 2022 Dec 28;12(1):236. doi: 10.3390/jcm12010236.
Non-classical mutations demonstrate heterogeneous and attenuated responsiveness to EGFR TKIs. Non-small cell lung cancer (NSCLC) patients with atypical mutations have limited therapeutic options. A recent study established a novel structural-based classification of mutations and showed its value in predicting the response to TKI. We sought to interrogate the distribution of different structural types and to validate the predictive value in Chinese NSCLCs. A total of 837 tumor samples were retrospectively recruited from 522 patients with unresectable -mutant NSCLC. mutations were classified into four groups: classical-like, T790M-like, Ex20ins-L, and PACC. Treatment information and clinical outcomes were obtained from 436 patients. The time to treatment failure (TTF) was determined on a per-sample basis. : Of the 837 -mutant samples, 67.9%, 18.5%, 9.0%, and 3.1% harbored classical-like, T790M-like, PACC, and Ex20ins-L mutations, respectively. Thirteen (1.6%) samples carried mutations beyond the four types. Among the 204 samples with atypical mutations, 33.8%, 36.7%, 12.7%, and 10.3% were classical-like, PACC, Ex20ins-L, and T790M-like, respectively. In patients with PACC mutations, second-generation TKIs demonstrated a significantly longer TTF than first-generation TKIs (first-line: 15.3 vs. 6.2 months, = 0.009; all-line: 14.7 vs. 7.1 months, = 0.003), and a trend of longer TTF than third-generation TKIs (all-line: 14.7 vs. 5.1 months, = 0.135). Our study depicted the landscape of structural types of mutations in Chinese NSCLC patients. Our results also suggest that the structural classification can serve as a predictive marker for the efficacy of various EGFR TKIs, which would guide therapeutic decision making.
非经典突变对表皮生长因子受体酪氨酸激酶抑制剂(EGFR TKIs)表现出异质性和减弱的反应性。具有非典型突变的非小细胞肺癌(NSCLC)患者的治疗选择有限。最近一项研究建立了基于结构的新型突变分类,并显示了其在预测对TKI反应方面的价值。我们试图探究不同结构类型的分布情况,并在中国非小细胞肺癌患者中验证其预测价值。从522例不可切除的EGFR突变型NSCLC患者中回顾性招募了总共837个肿瘤样本。EGFR突变被分为四组:类经典型、T790M样型、Ex20ins-L型和PACC型。从436例患者中获取了治疗信息和临床结果。按每个样本确定治疗失败时间(TTF)。结果显示:在837个EGFR突变样本中,分别有67.9%、18.5%、9.0%和3.1%携带类经典型、T790M样型、PACC型和Ex20ins-L型突变。13个(1.6%)样本携带了这四种类型之外的突变。在204个具有非典型突变的样本中,分别有33.8%、36.7%、12.7%和10.3%为类经典型、PACC型、Ex20ins-L型和T790M样型。在具有PACC突变的患者中,第二代TKI的TTF明显长于第一代TKI(一线治疗:15.3个月对6.2个月,P = 0.009;所有治疗线:14.7个月对7.1个月,P = 0.003),并且有比第三代TKI的TTF更长的趋势(所有治疗线:14.7个月对5.1个月,P = 0.135)。我们的研究描绘了中国NSCLC患者中EGFR突变的结构类型情况。我们的结果还表明,这种结构分类可作为各种EGFR TKI疗效的预测标志物,这将指导治疗决策。