PARP抑制剂
乳腺癌
癌症
医学
聚ADP核糖聚合酶
癌症研究
肿瘤科
内科学
生物信息学
计算生物学
生物
遗传学
DNA
聚合酶
标识
DOI:10.1158/2159-8290.cd-nw2024-0025
摘要
New data from the PETRA clinical trial suggest that the PARP1 inhibitor saruparib induces durable responses in patients with HER-negative breast cancer. Researchers found that the maximum tolerated dose of 90 mg per day produced an overall response rate of 46.7% and median duration of response of 5.6 months. The values for a dose of 60 mg were 48.4% and 7.3 months, leading the researchers to choose this as the optimal dose.
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