A 38-year-old woman presents to the genetics clinic with a personal history of triple-negative breast cancer diagnosed at age 35 and a family history of ovarian cancer in her mother at age 42. Genetic testing confirms a pathogenic mutation in BRCA1. The pedigree pattern shown in the diagram is labeled **B** (Hereditary breast-ovarian cancer). Which of the following management strategies is MOST appropriate to reduce her ovarian cancer risk in this BRCA1 carrier?
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