Zhou Wen, Yan Lu-Da, Yu Zhi-Qiong, Li Na, Yang Yong-Hua, Wang Meng, Chen Yuan-Yuan, Mao Meng-Xia, Peng Xiao-Chun, Cai Jun
Department of Oncology, First Affiliated Hospital of Yangtze University, Jingzhou, Hubei 434023, P.R. China.
Laboratory of Oncology, Center for Molecular Medicine, School of Basic Medicine, Health Science Center, Yangtze University, Jingzhou, Hubei 434023, P.R. China.
Oncol Lett. 2022 Jun;23(6):181. doi: 10.3892/ol.2022.13301. Epub 2022 Apr 15.
Anaplastic lymphoma kinase inhibitors have been shown to be effective in treating patients with -positive non-small cell lung cancer (NSCLC), and crizotinib, ceritinib and alectinib have been approved as clinical first-line therapeutic agents. The availability of these inhibitors has also largely changed the treatment strategy for advanced -positive NSCLC. However, patients still inevitably develop resistance to inhibitors, leading to tumor recurrence or metastasis. The most critical issues that need to be addressed in the current treatment of -positive NSCLC include the high cost of targeted inhibitors and the potential for increased toxicity and resistance to combination therapy. Recently, it has been suggested that the serine/threonine kinase 11 () mutation may serve as one of the biomarkers for immunotherapy in NSCLC. Therefore, the main purpose of this review was to summarize the role of in -positive NSCLC. The present review also summarizes the treatment and drug resistance studies in -positive NSCLC and the current status of research in NSCLC.
间变性淋巴瘤激酶抑制剂已被证明可有效治疗间变性淋巴瘤激酶阳性的非小细胞肺癌(NSCLC)患者,克唑替尼、色瑞替尼和阿来替尼已被批准为临床一线治疗药物。这些抑制剂的出现也在很大程度上改变了晚期间变性淋巴瘤激酶阳性NSCLC的治疗策略。然而,患者仍不可避免地对间变性淋巴瘤激酶抑制剂产生耐药性,导致肿瘤复发或转移。目前间变性淋巴瘤激酶阳性NSCLC治疗中需要解决的最关键问题包括靶向抑制剂的高成本以及联合治疗中潜在的毒性增加和耐药性。最近,有人提出丝氨酸/苏氨酸激酶11()突变可能作为NSCLC免疫治疗的生物标志物之一。因此,本综述的主要目的是总结在间变性淋巴瘤激酶阳性NSCLC中的作用。本综述还总结了间变性淋巴瘤激酶阳性NSCLC的治疗和耐药性研究以及NSCLC的研究现状。