Abstract

In the last years, Poly(ADP-ribose)-polymerase 1 inhibitors (PARPi) became a standard treatment option for patients with recurrent platinum-sensitive ovarian cancer and recently have been approved for maintenance use in the first-line setting. Biomarker subgroup analysis consistently revealed higher benefit for patients with homologous recombination deficiency (HRD; BRCA1/2m and/or genomic instability (GIS) positive), demonstrating the value of biomarker testing in this setting. The Myriad MyChoice assay has been the most commonly used HRD assay applied in the majority of clinical studies.

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