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Research Article| Volume 161, ISSUE 2, P521-526, May 2021

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Outcomes of incidentally detected ovarian cancers diagnosed at time of risk-reducing salpingo-oophorectomy in BRCA mutation carriers

  • Renee Cowan
    Affiliations
    Gynecology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA
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  • Silvana Pedra Nobre
    Affiliations
    Gynecology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA
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  • Nisha Pradhan
    Affiliations
    Clinical Genetics Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA
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  • Maya Yasukawa
    Affiliations
    Gynecology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA
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  • Qin C. Zhou
    Affiliations
    Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY, USA
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  • Alexia Iasonos
    Affiliations
    Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY, USA
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  • Robert A. Soslow
    Affiliations
    Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA

    Weill Medical College of Cornell University, New York, NY, USA
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  • Angela G. Arnold
    Affiliations
    Clinical Genetics Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA
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  • Magan Trottier
    Affiliations
    Clinical Genetics Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA
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  • Amanda Catchings
    Affiliations
    Clinical Genetics Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA
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  • Kara Long Roche
    Affiliations
    Gynecology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA

    Weill Medical College of Cornell University, New York, NY, USA
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  • Ginger Gardner
    Affiliations
    Gynecology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA

    Weill Medical College of Cornell University, New York, NY, USA
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  • Mark Robson
    Affiliations
    Clinical Genetics Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA

    Weill Medical College of Cornell University, New York, NY, USA

    Robert and Kate Niehaus Center for Inherited Cancer Genomics, Memorial Sloan Kettering Cancer Center, New York, NY, USA

    Gynecologic Medical Oncology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA
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  • Nadeem R. Abu Rustum
    Affiliations
    Gynecology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA

    Weill Medical College of Cornell University, New York, NY, USA
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  • Carol Aghajanian
    Affiliations
    Weill Medical College of Cornell University, New York, NY, USA

    Gynecologic Medical Oncology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA
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  • Karen Cadoo
    Correspondence
    Corresponding author: HOPe Directorate - St. James's Hospital, James Street, Dublin 8 D08 NHY1, Ireland.
    Affiliations
    Clinical Genetics Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA

    Weill Medical College of Cornell University, New York, NY, USA

    Robert and Kate Niehaus Center for Inherited Cancer Genomics, Memorial Sloan Kettering Cancer Center, New York, NY, USA

    Gynecologic Medical Oncology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA

    HOPe Directorate, St. James's Hospital, Dublin, Ireland
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      Highlights

      • A majority of OOC tumors are diagnosed at an early stage and have PFS and DSS consistent with what would be expected.
      • Women with an OOC diagnosed at the time of RRSO should be managed per stage-appropriate guidelines.
      • The OOC cohort was significantly older at RRSO, with a median age beyond that recommended for risk-reducing surgery.

      Abstract

      Objective

      Prior data suggested that women with incidentally detected occult invasive ovarian cancer (OIOC) at the time of risk-reducing salpingo-oophorectomy (RRSO) for BRCA mutation may have poorer prognoses than would be expected based on disease stage. We sought to evaluate prevalence and outcomes of patients with OIOC in a tertiary referral center.

      Methods

      Patients with BRCA mutation undergoing RRSO from 01/2005 to 05/2017 were identified, and their records reviewed. Women with incidentally detected OIOC were included; those with clinical features raising preoperative suspicion for malignancy were excluded.

      Results

      548 patients with BRCA mutation who underwent RRSO were identified. 26 (4.7%) had an OIOC (median age 55 years; range 42–75); 15(58%) patients, BRCA1; 9(34%), BRCA2; 2(8%) had a mutation in both genes. All OIOCs were high-grade serous: 10 (38%) Stage I; 8 (31%) Stage II; 8(31%) Stage III. 24(92%) patients received adjuvant platinum/taxane therapy. Of Stage III patients, 4 (50%) were identified intraoperatively; the remaining 4 (50%) had microscopic nodal disease on final pathology only. At median follow-up of 67.3 months (28–166) no Stage I patients have recurred; 2 Stage II and 6 Stage III patients recurred. 5-year progression-free survival (PFS) was 72% (95%CI, 50.2–85.7%); median PFS for the cohort was 129 months (95%CI, 75.3-not estimable). 5-year disease-specific survival (DSS) was 96% (95%CI, 76–99%); median DSS not reached.

      Conclusion

      Consistent with prior reports, almost 5% of patients had an OIOC at RRSO. The majority with early-stage disease had excellent PFS and DSS outcomes, as would be expected based on disease stage.

      Keywords

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