Department of Medical Oncology, Centro di Riferimento Oncologico di Aviano (CRO), IRCCS, 33081 Aviano, Italy.
Department of Medicine (DAME), University of Udine, 33100 Udine, Italy.
Int J Mol Sci. 2023 Jul 15;24(14):11495. doi: 10.3390/ijms241411495.
ROS proto-oncogene 1 (ROS1) rearrangements occur in 0.9-2.6% of patients with non small cell lung cancer (NSCLC), conferring sensitivity to treatment with specific tyrosine-kinase inhibitors (TKI). Crizotinib, a first-generation TKI, was the first target-therapy approved for the first-line treatment of ROS1-positive NSCLC. Recently, entrectinib, a multitarget inhibitor with an anti-ROS1 activity 40 times more potent than crizotinib and better activity on the central nervous system (CNS), received approval for treatment-naive patients. After a median time-to-progression of 5.5-20 months, resistance mechanisms can occur, leading to tumor progression. Therefore, newer generation TKI with greater potency and brain penetration have been developed and are currently under investigation. This review summarizes the current knowledge on clinicopathological characteristics of ROS1-positive NSCLC and its therapeutic options.
ROS 原癌基因 1(ROS1)重排在非小细胞肺癌(NSCLC)患者中的发生率为 0.9-2.6%,使其对特定的酪氨酸激酶抑制剂(TKI)敏感。克唑替尼是第一代 TKI,是第一种被批准用于 ROS1 阳性 NSCLC 一线治疗的靶向治疗药物。最近,恩曲替尼,一种具有抗 ROS1 活性的多靶点抑制剂,其活性比克唑替尼强 40 倍,对中枢神经系统(CNS)的活性更好,被批准用于未经治疗的患者。在中位无进展时间为 5.5-20 个月后,可能会发生耐药机制,导致肿瘤进展。因此,已经开发出并正在研究具有更强效力和脑穿透性的新一代 TKI。这篇综述总结了 ROS1 阳性 NSCLC 的临床病理特征及其治疗选择的最新知识。