Homologous recombination deficiency and VEGF expression are key pathways in high-grade ovarian cancer. Recently, three randomized practice changing trials were published: the PAOLA-1, PRIMA and VELIA trials. The use of PARP inhibitors (PARPi) following chemotherapy has become standard of care in first line. Combination of PARPi with anti-angiogenic agents has demonstrated synergistic activity in preclinical study. This review summarizes the body of evidence supporting the efficacy and safety of the combination of PARPi and anti-angiogenic drugs in first-line homologous recombination deficiency high-grade ovarian cancer leading to US FDA and EMA approvals. This double maintenance is supported by: a large benefit with bevacizumab + olaparib compared with olaparib alone, a rationale for additive effect, and a good safety and cost-effective profile.

Download full-text PDF

Source
http://dx.doi.org/10.2217/fon-2021-0059DOI Listing

Publication Analysis

Top Keywords

ovarian cancer
12
anti-angiogenic agents
8
homologous recombination
8
high-grade ovarian
8
polyadp-ribose polymerase inhibitors
4
polymerase inhibitors combination
4
combination anti-angiogenic
4
agents treatment
4
treatment advanced
4
advanced ovarian
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!