PALB2
PARP抑制剂
奥拉帕尼
癌症研究
医学
前列腺
内科学
肿瘤科
聚ADP核糖聚合酶
生物
突变
癌症
遗传学
基因
种系突变
聚合酶
出处
期刊:Cancer Discovery
[American Association for Cancer Research]
日期:2022-05-26
卷期号:12 (7): 1602-1602
被引量:9
标识
DOI:10.1158/2159-8290.cd-nb2022-0039
摘要
Findings from the phase I/IIa trial of AZD5305, a next-generation, highly selective PARP1 inhibitor, indicate that the drug is better tolerated in patients with ovarian, HER2-negative breast, pancreatic, and prostate cancers with BRCA1/2, PALB2, and RAD51C mutations compared with first-generation PARP inhibitors. In addition, 25% of 40 evaluable patients had a partial response.
科研通智能强力驱动
Strongly Powered by AbleSci AI