Cancer Discov. 2017 Feb;7(2):120-121. doi: 10.1158/2159-8290.CD-NB2016-164. Epub 2017 Jan 5.
The FDA approved the PARP inhibitor rucaparib to treat women with advanced ovarian cancer who have already been treated with at least two chemotherapies and have a BRCA1 or BRCA2 gene mutation identified by an approved companion diagnostic test. The agency also gave a nod to the FoundationFocus CDxBRCA test to detect BRCA alterations.
美国食品药品监督管理局(FDA)批准 PARP 抑制剂芦卡帕利(rucaparib)用于治疗至少接受过两种化疗且经获批伴随诊断检测识别出 BRCA1 或 BRCA2 基因突变的晚期卵巢癌女性。该机构还批准了 FoundationFocus CDxBRCA 检测法,以检测 BRCA 改变。