医学
中止
间变性淋巴瘤激酶
碱性抑制剂
融合基因
癌症研究
突变
酪氨酸激酶
肿瘤科
酪氨酸激酶抑制剂
内科学
基因
遗传学
癌症
生物
受体
恶性胸腔积液
肺癌
作者
Kaushal Parikh,Anastasios Dimou,Konstantinos Leventakos,Aaron S. Mansfield,Mohamed Shanshal,Yin Wan,Huamao Mark Lin,Sylvie Vincent,Jennifer Elliott,Ioana Bonta
标识
DOI:10.1016/j.jtho.2024.07.009
摘要
Tyrosine kinase inhibitors (TKIs) are first-line treatment options for ALK-positive (ALK+) non-small cell lung cancer (NSCLC). Factors such as variant allele frequencies (VAF), EML4-ALK fusion variant, and concurrent TP53 mutations (TP53mt) in circulating tumor DNA (ctDNA) may affect treatment outcomes. We evaluated their effects on time to discontinuation (TTD) of first-line treatment with next-generation ALK TKIs in a real-world setting.
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