Du Mingyuan, Liu Cuiwei, Chen Leichong, Li Zhenyu, Zhang Sijia, Meng Rui
Cancer Center, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Hubei Key Laboratory of Precision Radiation Oncology, Wuhan, China.
Clin Respir J. 2024 Dec;18(12):e70041. doi: 10.1111/crj.70041.
Lung cancer treatment has evolved at the molecular level. Detecting the presence of driver genes in lung cancer fundamentally alters the choice of therapeutic regimens and the outcome of this disease. ALK fusion mutation is one of the most important mutations in nonsmall cell lung cancer (NSCLC). Also, it often has other coexisting mutation types. TP53 is the most common coexisting mutation type, whereas the EGFR/ALK coexisting mutation type is extremely rare. There is still no definite conclusion about the impact of the multimutation and best treatment options for NSCLC patients with advanced multimutation. In this study, we report three cases of NSCLC with ALK fusion mutations as well as ALK combined with TP53 mutations and ALK combined with EGFR mutations. Combining cases from our oncology center and previous literature, we found that NSCLC patients with coexisting ALK fusion mutations and other mutations have poorer response to targeted therapy and poorer prognosis, and we also compared the efficacy rates of various types of coexisting mutations for different treatment regimens. Therefore, this review can help to evaluate the prognosis of NSCLC patients with coexisting mutations and the efficacy of targeted therapies and to find more favorable treatment options for patients with this type of coexisting mutations.
肺癌治疗在分子层面上不断发展。检测肺癌中驱动基因的存在从根本上改变了治疗方案的选择以及该病的治疗结果。ALK融合突变是非小细胞肺癌(NSCLC)中最重要的突变之一。此外,它常常还伴有其他共存的突变类型。TP53是最常见的共存突变类型,而EGFR/ALK共存突变类型极为罕见。对于晚期多基因突变的NSCLC患者,多基因突变的影响以及最佳治疗方案尚无定论。在本研究中,我们报告了3例伴有ALK融合突变以及ALK与TP53联合突变和ALK与EGFR联合突变的NSCLC病例。结合我们肿瘤中心的病例和既往文献,我们发现共存ALK融合突变和其他突变的NSCLC患者对靶向治疗的反应较差且预后较差,并且我们还比较了不同治疗方案下各种共存突变类型的有效率。因此,本综述有助于评估共存突变的NSCLC患者的预后以及靶向治疗的疗效,并为这类共存突变患者找到更有利的治疗方案。