Xie Jiajun, Gao Yinghao, Xu Weiguo, Zhu Jing
Department of Respiratory and Critical Care Medicine, Mian yang Central Hospital, School of Medicine, University of Electronic Science and Technology of China, Mianyang, People's Republic of China.
Department of pulmonology, Mianyang hospital of T.C.M, Mianyang, People's Republic of China.
Int J Gen Med. 2025 Apr 15;18:2151-2171. doi: 10.2147/IJGM.S512395. eCollection 2025.
Lung cancer continues to be a leading cause of cancer-related mortality and morbidity worldwide. The echinoderm microtubule-associated protein-like 4-anaplastic lymphoma kinase (EML4-ALK) fusion gene accounts for approximately 3%-5% of gene mutation types. Targeted therapies for ALK mutations have made significant advancements in recent decades, enabling a considerable number of patients to achieve the goal of five-year survival benefits. However, overcoming the drug resistance that arises with current ALK tyrosine kinase inhibitors (TKIs) remain a major challenge in ALK-targeted therapies. In this review, we briefly discuss the primary and secondary mechanisms of resistance to ALK-TKIs, and explore treatment strategies based on progressive resistance models. Meanwhile, novel drugs and combination therapies are being actively researched and developed to address these challenges. The aim is to offer new insights into the mechanisms of resistance and the corresponding treatment strategies to ALK inhibitors.
肺癌仍然是全球癌症相关死亡和发病的主要原因。棘皮动物微管相关蛋白样4-间变性淋巴瘤激酶(EML4-ALK)融合基因约占基因突变类型的3%-5%。近几十年来,针对ALK突变的靶向治疗取得了重大进展,使相当数量的患者实现了五年生存获益的目标。然而,克服当前ALK酪氨酸激酶抑制剂(TKIs)产生的耐药性仍然是ALK靶向治疗中的一项重大挑战。在本综述中,我们简要讨论了对ALK-TKIs耐药的主要和次要机制,并基于渐进性耐药模型探索治疗策略。同时,正在积极研发新型药物和联合疗法来应对这些挑战。目的是为ALK抑制剂的耐药机制及相应治疗策略提供新的见解。