Wang Lifeng, Liu Zichen, Wan Zhiyi, Jiang Dong, Zhang Min, Liu Shuku, Che Nanying
Department of Pathology, Chongqing University Cancer Hospital and Chongqing Cancer Institute and Chongqing Cancer Hospital, Chongqing, China.
Department of Pathology, Beijing Chest Hospital, Capital Medical University, Beijing Tuberculosis and Thoracic Tumor Research Institute, Beijing, China.
Ann Transl Med. 2022 Feb;10(4):220. doi: 10.21037/atm-22-383.
Epidermal growth factor receptor exon 20 insertions ( ex20ins) occur in about 4-14% of lung adenocarcinoma (LUAD) patients with mutations. Recently some targeted drugs have been approved for the treatment of LUAD patients with ex20ins. However, the heterogeneity of ex20ins mutations and resultant challenges in identifying them have led to the underestimation of their frequency.
We investigated the molecular and clinicopathologic features of ex20ins in 3,892 Chinese LUAD patients using next-generation sequencing (NGS). The frequency and distribution of ex20ins mutations between Chinese and Western LUAD patients were also compared by integrating the data of this study and the data of previous studies.
A total of 23 unique ex20ins were identified in 77 LUAD patients, accounting for 1.98% of all LUAD patients and 3.49% of mutant LUDA patients. The 2 most common ex20ins subtypes were S768_D770dup and A767_V769dup, which together accounted for 55.84% of the ex20ins cases. About 61% (14/23) of the ex20ins subtypes occurred only once. Additionally, 8 of the ex20ins subtypes were not recorded in the COSMIC database. These results showed that the ex20ins mutations were highly heterogeneous. There was no significant difference in the frequency and distribution of ex20ins mutations between Chinese and Western LUAD patients, but the frequency of ex20ins mutations was significantly lower in -mutant Chinese LUAD patients than Western LUAD patients. The co-mutation analysis showed that ex20ins occurred significantly and exclusively with certain driver genes in LUAD, including fusion (χ=7.133, P=0.008), (χ=8.468, P=0.004), and (χ=5.792, P=0.016). No gene was observed to be significantly co-mutated with ex20ins. In general, patients with ex20ins shared a similar age and gender to patients with other mutations or without ex20ins.
Overall, our results revealed the molecular and clinicopathologic features of ex20ins in Chinese LUAD patients, which will be helpful for drug development and in clinical trials targeting ex20ins.
表皮生长因子受体外显子20插入(ex20ins)发生在约4%-14%的伴有基因突变的肺腺癌(LUAD)患者中。最近,一些靶向药物已被批准用于治疗伴有ex20ins的LUAD患者。然而,ex20ins突变的异质性以及识别它们所带来的挑战导致其频率被低估。
我们使用下一代测序(NGS)研究了3892例中国LUAD患者中ex20ins的分子和临床病理特征。通过整合本研究的数据和先前研究的数据,还比较了中国和西方LUAD患者中ex20ins突变的频率和分布。
在77例LUAD患者中总共鉴定出23种独特的ex20ins,占所有LUAD患者的1.98%,占LUAD突变患者的3.49%。2种最常见的ex20ins亚型是S768_D770dup和A767_V769dup,它们共同占ex20ins病例的55.84%。约61%(14/23)的ex20ins亚型仅出现一次。此外,COSMIC数据库中未记录8种ex20ins亚型。这些结果表明ex20ins突变具有高度异质性。中国和西方LUAD患者中ex20ins突变的频率和分布没有显著差异,但中国LUAD突变患者中ex20ins突变的频率显著低于西方LUAD患者。共突变分析表明,ex20ins在LUAD中与某些驱动基因显著且排他地同时发生,包括ALK融合(χ²=7.133,P=0.008)、KRAS(χ²=8.468,P=0.004)和NRAS(χ²=5.792,P=0.016)。未观察到与ex20ins显著共突变的基因。总体而言,伴有ex20ins的患者与伴有其他基因突变或不伴有ex20ins的患者在年龄和性别上相似。
总体而言,我们的结果揭示了中国LUAD患者中ex20ins的分子和临床病理特征,这将有助于针对ex20ins的药物开发和临床试验。