New advances in understanding the mechanisms and treatment challenges of ALK-targeted therapy resistance in lung cancer.

IF 4.6 Q1 ONCOLOGY
癌症耐药(英文) Pub Date : 2025-08-25 eCollection Date: 2025-01-01 DOI:10.20517/cdr.2025.122
Mengle Long, Shixuan Peng, Qingyang Wen, Zhijian Yin, Xinwen Zhang, Haoyu Tan, Yun Xu, Yongjun Wu
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Abstract

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.

肺癌alk靶向治疗耐药机制和治疗挑战的新进展。
尽管开发了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主要挑战。靶内和脱靶机制都被确定为耐药性的关键因素。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)患者的预后和生存得到改善。然而,即使是第二代和第三代alk - tki,克服阻力仍然很困难。在批准的治疗中经常出现耐药性,这强调了进一步研究阐明与alk阳性肺癌相关的分子事件和耐药机制的必要性。间变性淋巴瘤激酶(ALK)重排作为NSCLC可操作的致癌驱动因素的发现,为晚期疾病建立了生物标志物驱动的治疗范式。本文综述了目前对肺癌alk靶向治疗耐药机制的了解,包括原发性和获得性机制、耐药后的治疗策略、最近的治疗进展以及免疫系统和肿瘤微环境的影响。深入了解ALK靶向治疗耐药对于制定新的治疗策略至关重要,并可能为指导耐药ALK+肺癌患者的诊断、治疗和管理提供重要见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
6.60
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