前列腺癌
医学
聚ADP核糖聚合酶
PARP抑制剂
合成致死
癌症研究
同源重组
DNA修复
癌症
DNA损伤修复
前列腺
内科学
肿瘤科
聚合酶
DNA
生物
遗传学
作者
Arshit Narang,Chadi Hage Chehade,Zeynep İrem Özay,Blake Nordblad,Umang Swami,Neeraj Agarwal
标识
DOI:10.1080/14656566.2024.2397002
摘要
Despite recent therapeutic advancements, mCRPC remains a lethal disease. Androgen receptor pathway inhibitors (ARPIs) are approved for patients with mCRPC and mHSPC, yet most patients first receive these agents in the castration-resistant setting. Real-world data indicate that around half of patients with mCRPC do not receive subsequent lines of therapy, underscoring the efficacy of upfront combination therapies. The combinations of ARPI plus PARPi are indicated for patients with mCRPC harboring HRR mutations, though identifying these patients is challenging due to limited genomic testing. Further research and improved access to genomic testing are essential to optimize treatment strategies.
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