[Expert consensus on iruplinalkib for the treatment of <i>ALK</i>-positive non-small cell lung cancer (2026 edition)].
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Abstract
Anaplastic lymphoma kinase (<i>ALK</i>) fusion gene is one of the most common driver genes in non-small cell lung cancer (NSCLC). ALK-tyrosine kinase inhibitors (TKIs) have become the standard treatment option for patients with advanced <i>ALK</i> gene fusion positive NSCLC. Currently, the China National Medical Products Administration (NMPA) has approved ten ALK-TKIs, including crizotinib, ceritinib, alectinib, ensartinib, brigatinib, lorlatinib, iruplinalkib, envonalkib, dirozalkib and conteltinib. Iruplinalkib is a novel ALK-TKI independently developed in China. On June 27, 2023, the NMPA approved iruplinalkib for the treatment of patients with locally advanced or metastatic <i>ALK</i>-positive NSCLC who had progressed on or were intolerant to crizotinib. On January 16, 2024, the NMPA approved iruplinalkib for first-line treatment of patients with locally advanced or metastatic <i>ALK</i>-positive NSCLC patients. To help clinicians better understand the efficacy and safety of iruplinalkib and to facilitate its more rational clinical application, the Medical Oncology Branch of China International Exchange and Promotive Association for Medical and Health Care and the Chinese Association for Clinical Oncologists organized experts to develop the "Expert consensus on iruplinalkib for the treatment of <i>ALK</i>-positive non-small cell lung cancer (2026 edition)". This consensus provides systematic and comprehensive update of clinical research data on iruplinalkib published before June 25, 2026, based on the 2024 edition. It covers common clinical issues and provides corresponding recommendations for the use of iruplinalkib in the treatment of <i>ALK</i>-positive NSCLC. 间变性淋巴瘤激酶(ALK)融合基因是非小细胞肺癌(NSCLC)常见的驱动基因之一。ALK酪氨酸激酶抑制剂(TKIs)已经成为ALK融合基因阳性晚期NSCLC患者的标准治疗选择。目前中国国家药品监督管理局已经批准10种ALK-TKIs上市,分别是克唑替尼、塞瑞替尼、阿来替尼、恩沙替尼、布格替尼、洛拉替尼、伊鲁阿克、依奉阿克、地罗阿克和康特替尼。伊鲁阿克是中国自主研发的新型ALK-TKI。2023年6月27日,中国国家药品监督管理局批准伊鲁阿克上市,用于既往接受过克唑替尼治疗后疾病进展或对克唑替尼不耐受的ALK融合基因阳性局部晚期或转移性NSCLC患者的治疗,2024年1月16日,中国国家药品监督管理局批准伊鲁阿克用于ALK融合基因阳性局部晚期或转移性NSCLC患者的一线治疗。为了帮助广大医师更好地了解伊鲁阿克的疗效和安全性,使伊鲁阿克得到更合理的临床应用,中国医疗保健国际交流促进会肿瘤内科学分会和中国医师协会肿瘤医师分会组织专家编写了《伊鲁阿克治疗间变性淋巴瘤激酶融合基因阳性非小细胞肺癌专家共识(2026版)》。共识在2024版的基础上对2026年6月25日之前发表的伊鲁阿克临床研究数据进行了系统、全面的更新,涵盖了伊鲁阿克治疗ALK阳性非小细胞肺癌过程中常见的临床问题和相应指导建议。.Source: PubMed (PMID: 42502071)View Original on PubMed