Zhan Shuting, Li Jianfu, Cheng Bo, Li Caichen, Feng Yi, Fan Lei, Xiong Shan, Zeng Wenchuang, Cai Qi, Xiang Yang, Wang Huiting, Li Chunyan, Chen Peiling, Zheng Xin, Fu Wenhai, Hao Zhexue, He Jianxing, Liang Wenhua
Department of Thoracic Surgery and Oncology, The First Affiliated Hospital of Guangzhou Medical University and Guangzhou Institute of Respiratory Health, Guangzhou, China.
State Key Laboratory of Respiratory Disease and National Clinical Research Center for Respiratory Disease, Guangzhou, China.
Ther Adv Med Oncol. 2024 Sep 25;16:17588359241279715. doi: 10.1177/17588359241279715. eCollection 2024.
Real-world data on C-MET protein overexpression in non-small cell lung cancer (NSCLC) patients, particularly among the Asian Chinese population, are limited.
This study aimed to evaluate the clinicomolecular characteristics and prognosis of C-MET overexpression in Chinese NSCLC patients, focusing on those with positive C-MET overexpression (immunohistochemistry (IHC) 3+).
A retrospective and observational study.
Data were collected from NSCLC patients diagnosed at the First Affiliated Hospital of Guangzhou Medical University between November 2006 and April 2021. We identified C-MET overexpression using IHC and C-MET overexpression positivity was defined as IHC 3+ with ⩾50% tumor cells. Additionally, patient genotypes were collected for subgroup analysis.
Data from 9785 NSCLC patients were collected. C-MET (-) accounted for 5% (503/9785), C-MET (+) for 27% (2654/9785), C-MET (++) for 36% (3464/9785), and C-MET (+++) for 32% (3164/9785). Genetic testing was available for 4326 patients. Wild-type was observed in 37% (1591 cases), with epidermal growth factor receptor () abnormalities being the most common at 49% (2127 cases). Positive C-MET overexpression correlated significantly with women ( < 0.001), early-stage ( = 0.003), adenocarcinoma ( < 0.001), and driver mutations ( < 0.001). Patients with anaplastic lymphoma kinase () alterations had a higher occurrence of C-MET overexpression positivity (57.1%). Positive C-MET overexpression was significantly associated with ( < 0.001), ( < 0.001), and alterations ( = 0.024). Compared to C-MET overexpression (IHC 0), C-MET overexpression (IHC 2+) (hazard ratio (HR) = 0.455, < 0.001) and C-MET overexpression (IHC 3+) (HR = 0.569, < 0.001) were correlated with better overall survival in overall NSCLC patients, especially for C-MET overexpression (IHC 2+).
Our study elucidates the clinicomolecular characteristics and prognosis of C-MET overexpression in NSCLC patients, particularly those with positive C-MET overexpression (IHC 3+). This provides insight into the prevalence of C-MET overexpression in Chinese NSCLC patients and offers a basis for considering C-MET overexpression as a prognostic and predictive marker in NSCLC.
关于非小细胞肺癌(NSCLC)患者中C-MET蛋白过表达的真实世界数据有限,尤其是在亚洲中国人群中。
本研究旨在评估中国NSCLC患者中C-MET过表达的临床分子特征和预后,重点关注C-MET过表达阳性(免疫组织化学(IHC)3+)的患者。
一项回顾性观察研究。
收集2006年11月至2021年4月在广州医科大学附属第一医院诊断的NSCLC患者的数据。我们使用IHC鉴定C-MET过表达,C-MET过表达阳性定义为IHC 3+且肿瘤细胞≥50%。此外,收集患者基因型进行亚组分析。
收集了9785例NSCLC患者的数据。C-MET(-)占5%(503/9785),C-MET(+)占27%(2654/9785),C-MET(++)占36%(3464/9785),C-MET(+++)占32%(3164/9785)。4326例患者可进行基因检测。37%(1591例)观察到野生型,其中表皮生长因子受体()异常最为常见,占49%(2127例)。C-MET过表达阳性与女性(<0.001)、早期(=0.003)、腺癌(<0.001)和驱动基因突变(<0.001)显著相关。间变性淋巴瘤激酶()改变的患者C-MET过表达阳性发生率更高(57.1%)。C-MET过表达阳性与(<0.001)、(<0.001)和改变(=0.024)显著相关。与C-MET过表达(IHC 0)相比,C-MET过表达(IHC 2+)(风险比(HR)=0.455,<0.001)和C-MET过表达(IHC 3+)(HR=0.569,<0.001)与总体NSCLC患者更好的总生存期相关,尤其是C-MET过表达(IHC 2+)。
我们的研究阐明了NSCLC患者中C-MET过表达的临床分子特征和预后,尤其是C-MET过表达阳性(IHC 3+)的患者。这为了解中国NSCLC患者中C-MET过表达的患病率提供了见解,并为将C-MET过表达作为NSCLC的预后和预测标志物提供了依据。