| Literature DB >> 31242303 |
Koji Matsumoto1,2, Meiko Nishimura1,2, Takuma Onoe1,2, Hideki Sakai1, Yusaku Urakawa2, Takashi Onda3, Nobuo Yaegashi4.
Abstract
After a brief summary of the current status of poly-ADP ribose polymerase (PARP) inhibitors for ovarian cancer, we summarize the current status of PARP inhibitors for BRCA wild type ovarian cancer, especially regarding gene alterations other than BRCA, homologous recombination deficiency (HRD), and combinations. Discussion of gene alterations other than BRCA include the results of multiple gene panels studying homologous recombination repair deficiency genes and cancer susceptibility genes, and influences of these alterations on efficacy of PARP inhibitors and cancer susceptibility. Discussions of HRD include the results of phase three trials using HRD assay, the definition of HRD assays, and the latest assays. Discussions of combinations include early phase trial results and ongoing trials combining PARP inhibitors with immune checkpoint inhibitors, anti-angiogenic agents, and triplets.Entities:
Keywords: zzm321990 BRCA wild type; HRD; LOH; PARP inhibitors; genetic counseling
Year: 2019 PMID: 31242303 DOI: 10.1093/jjco/hyz090
Source DB: PubMed Journal: Jpn J Clin Oncol ISSN: 0368-2811 Impact factor: 3.019