PARP抑制剂
癌症研究
酪氨酸激酶抑制剂
PALB2
种系突变
DNA修复
突变
腺癌
生殖系
同源重组
医学
聚ADP核糖聚合酶
内科学
生物
癌症
DNA
遗传学
基因
聚合酶
作者
Chao Zhu,Peng Xu,Linheng Li,Hongmei Wei
出处
期刊:Anti-Cancer Drugs
[Lippincott Williams & Wilkins]
日期:2025-03-03
卷期号:36 (6): 518-520
被引量:1
标识
DOI:10.1097/cad.0000000000001712
摘要
Tumors with homologous recombination deficiency (HRD) can benefit from treatment with poly ADP-ribose polymerase inhibitors (PARPi). However, the methods for identifying HRD vary and are controversial. Several DNA repair genes in the homologous recombination repair pathway may be linked to PARPi susceptibility, and studies are underway to identify biomarkers that can predict the response to PARPi. We present a case of EGFR-tyrosine kinase inhibitor-resistant metastatic lung adenocarcinoma with a germline PALB2 mutation that was treated with fluzoparib (an orally administered PARPi). The treatment achieved surprising results and lasted for more than 4.5 months. Our study provided evidence that metastatic lung adenocarcinoma with germline PALB2 could benefit from PARPi, which improves patient outcomes.
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