Long Mengle, Peng Shixuan, Wen Qingyang, Yin Zhijian, Zhang Xinwen, Tan Haoyu, Xu Yun, Wu Yongjun
Department of Oncology, Graduate Collaborative Training Base of The First People's Hospital of Xiangtan City, Hengyang Medical School, University of South China, Hengyang 421001, Hunan, China.
Department of Oncology, The First People's Hospital of Xiangtan City, Xiangtan 411101, Hunan, China.
Cancer Drug Resist. 2025 Aug 25;8:43. doi: 10.20517/cdr.2025.122. eCollection 2025.
Despite the development of various effective anaplastic lymphoma kinase tyrosine kinase inhibitors (ALK-TKIs), therapeutic resistance remains a major challenge. Both on-target and off-target mechanisms have been identified as key contributors to resistance. With the popularization of genetic testing and the development of precision therapies, the prognosis and survival of patients with ALK-positive non-small cell lung cancer (NSCLC) have improved. However, even with second- and third-generation ALK-TKIs, overcoming resistance remains difficult. Resistance frequently arises during approved treatments, underscoring the need for further research to elucidate the molecular events and resistance mechanisms associated with ALK-positive lung cancer. The discovery of anaplastic lymphoma kinase (ALK) rearrangement as an actionable oncogenic driver in NSCLC has established a biomarker-driven treatment paradigm for advanced disease. This article summarizes current knowledge of the mechanisms of resistance to ALK-targeted therapy in lung cancer, including both primary and acquired mechanisms, treatment strategies following resistance, recent therapeutic advances, and the impact of the immune system and tumor microenvironment. A deeper understanding of ALK-targeted therapy resistance is critical for developing new treatment strategies and may provide important insights to guide the diagnosis, treatment, and management of patients with resistant ALK lung cancer.
尽管已经开发出各种有效的间变性淋巴瘤激酶酪氨酸激酶抑制剂(ALK-TKIs),但治疗耐药性仍然是一个重大挑战。靶向和非靶向机制均已被确定为耐药的关键因素。随着基因检测的普及和精准治疗的发展,ALK阳性非小细胞肺癌(NSCLC)患者的预后和生存率有所改善。然而,即使使用第二代和第三代ALK-TKIs,克服耐药性仍然困难。耐药性常常在批准的治疗过程中出现,这突出表明需要进一步研究以阐明与ALK阳性肺癌相关的分子事件和耐药机制。间变性淋巴瘤激酶(ALK)重排作为NSCLC中一种可操作的致癌驱动因素的发现,为晚期疾病建立了一种生物标志物驱动的治疗模式。本文总结了目前关于肺癌中ALK靶向治疗耐药机制的知识,包括原发性和获得性机制、耐药后的治疗策略、近期治疗进展以及免疫系统和肿瘤微环境的影响。深入了解ALK靶向治疗耐药性对于开发新的治疗策略至关重要,并且可能为指导耐药性ALK肺癌患者的诊断、治疗和管理提供重要见解。