Lu Zhiqin, Cai Jing, Zeng Zhimin, Liu Anwen
Department of Oncology, The Second Affiliated of Nanchang University, Nanchang 330006, China.
Jiangxi Key Laboratory of Clinical Translational Cancer Research, Nanchang 330006, China.
Zhongguo Fei Ai Za Zhi. 2020 Aug 20;23(8):710-718. doi: 10.3779/j.issn.1009-3419.2020.102.18. Epub 2020 Aug 6.
Leptomeningeal metastasis (LM) is one of the serious complications of advanced non-small cell lung cancer (NSCLC), although the incidence is not high, the clinical symptoms are severe and the prognosis is poor. LM is prone to occur in patients with positive driver gene than negative. At present, the treatment of LM mainly includes molecular targeted therapy, systemic chemotherapy, whole brain radiotherapy, intrathecal chemotherapy and immunotherapy. Although there are many treatments, the efficacy of LM is still unsatisfactory. This article reviews the drug therapy of sensitive driver gene positive NSCLC LM.
软脑膜转移(LM)是晚期非小细胞肺癌(NSCLC)的严重并发症之一,尽管其发病率不高,但临床症状严重且预后较差。与驱动基因阴性的患者相比,驱动基因阳性的患者更容易发生LM。目前,LM的治疗主要包括分子靶向治疗、全身化疗、全脑放疗、鞘内化疗和免疫治疗。尽管有多种治疗方法,但LM的疗效仍不尽人意。本文综述了敏感驱动基因阳性NSCLC-LM的药物治疗。