178 Risk-reducing salpingo-oophorectomy in BRCA mutation patients

Introduction/BackgroundBRCA1/2 are tumour-suppressor genes involved in DNA homologous recombination and ovarian cancer development. The study evaluated the risk of tumor cancer in women presenting the BRCA mutations.MethodologyRisk-reducing surgery (RRS) was performed in all patients carrying BRCA1...

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Published inInternational journal of gynecological cancer Vol. 33; no. Suppl 3; p. A342
Main Authors Loizzi, Vera, Arezzo, Francesca, Mongelli, Michele, Kardhashi, Anila, Silvestris, Erica, Cazzolla, Ambrogio, Difonzo, Tommaso, Cerbone, Marco, Battista, Gaia, Quarto, Pietro, Memmola, Massimiliano, Cormio, Gennaro
Format Journal Article
LanguageEnglish
Published Oxford BMJ Publishing Group LTD 01.09.2023
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Summary:Introduction/BackgroundBRCA1/2 are tumour-suppressor genes involved in DNA homologous recombination and ovarian cancer development. The study evaluated the risk of tumor cancer in women presenting the BRCA mutations.MethodologyRisk-reducing surgery (RRS) was performed in all patients carrying BRCA1 (aged between 30–73 years, median age was 51 years) and BRCA 2 mutation (aged between 36–70 years, median age was 53 years) referred at University of Bari, Italy. Fifty-eight percent of the patient population had previous history of breast cancer.ResultsOne hundred and ninty-one patients underwent risk-reducing surgery (RRS) for their BRCA1/2 mutations. Of them, 82% of the women underwent risk-reducing salpingo-oophorectomy (RRSO) through a laparoscopic minimally invasive approach, 7% underwent laparoscopic RRSO and contextual hysterectomy, 1% underwent RRSO through a laparotomic approach and 10 a laparotomic RRSO and hysterectomy. During laparoscopic RRSO, 5% of the patients underwent a prophylactic bilateral mastectomy. Early and late complication occurred in only 2 women. Five patients (3%) were found to have occult Serous Tubal Intraepithelial Carcinoma (STIC) and seven patients (4%) occult cancer.ConclusionRRSO is safe and feasible in BRCA 1/2 mutation carriers. The procedure is effective for genetic prevention of ovarian cancer.DisclosuresNo discosures
ISSN:1048-891X
1525-1438
DOI:10.1136/ijgc-2023-ESGO.721