阿列克替尼
克里唑蒂尼
间变性淋巴瘤激酶
腺癌
融合基因
肺癌
肿瘤科
医学
癌症研究
内科学
阶段(地层学)
癌症
生物
基因
遗传学
古生物学
恶性胸腔积液
作者
Minhua Zheng,Cunliang Cai,Jiayi Yao,Jie Zhao,Ming‐Qiang Zhang,Fei Liu,Xin Mu
标识
DOI:10.3389/fgene.2023.1289346
摘要
The prevalence of Anaplastic Lymphoma Kinase gene ( ALK ) fusion is about 5% among patients with lung adenocarcinoma, underscoring the importance of pinpointing distinct fusion variants for optimizing treatment approaches. This is the first reported case of a 74-year-old female with stage IV lung adenocarcinoma, featuring a novel Kinesin Family Member 13A ( KIF13A ) -ALK fusion, identified via next-generation sequencing (NGS) and confirmed with fluorescence in situ hybridization (FISH). Initially undergoing chemotherapy and then crizotinib, she achieved a partial response (PR) before progressing with multiple bone metastases. However, subsequent treatment with alectinib as a third-line option yielded positive results. A stable disease state persisted for an impressive 31 months of progression-free survival (PFS), accompanied by minimal toxicity symptoms. Up until now, a remarkable near 4-year span of overall survival (OS) has been consistently observed and monitored. This report of a KIF13A-ALK fusion case benefit significantly from alectinib with extensive follow-up. The case diversifies the array of ALK fusion partners and holds clinical relevance in refining therapeutic choices for KIF13A-ALK fusion-associated lung cancer.
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