Ontology highlight
ABSTRACT: Background
High-grade serous ovarian cancers show increased replication stress, rendering cells vulnerable to ATR inhibition because of near universal loss of the G1/S checkpoint (through deleterious TP53 mutations), premature S phase entry (due to CCNE1 amplification, RB1 loss, or CDKN2A mRNA downregulation), alterations of homologous recombination repair genes, and expression of oncogenic drivers (through MYC amplification and other mechanisms). We hypothesised that the combination of the selective ATR inhibitor, berzosertib, and gemcitabine could show acceptable toxicity and superior efficacy to gemcitabine alone in high-grade serous ovarian cancer.Methods
In this multicentre, open-label, randomised, phase 2 study, 11 different centres in the US Experimental Therapeutics
SUBMITTER: Konstantinopoulos PA
PROVIDER: S-EPMC8023719 | biostudies-literature | 2020 Jul
REPOSITORIES: biostudies-literature