Publication:
Clinical significance of risk-reducing salpingo-oophorectomy in patients with BRCA1/2 mutation

dc.contributor.authorAbay, Merve
dc.contributor.authorÖzgen, Levent
dc.contributor.authorYalçın, Yakup
dc.contributor.authorÖzerkan, Kemal
dc.contributor.buuauthorABAY, MERVE
dc.contributor.buuauthorÖZGEN, LEVENT
dc.contributor.buuauthorYALÇIN, YAKUP
dc.contributor.buuauthorÖZERKAN, KEMAL
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentKadın Hastalıkları ve Doğum Ana Bilim Dalı
dc.contributor.orcid0000-0003-0070-2646
dc.contributor.researcheridCAK-3842-2022
dc.contributor.researcheridJFT-0660-2023
dc.contributor.researcheridHQP-3191-2023
dc.contributor.researcheridAAH-9791-2021
dc.date.accessioned2024-06-14T06:17:56Z
dc.date.available2024-06-14T06:17:56Z
dc.date.issued2023-10
dc.description.abstractObjective: Serous tubal intraepithelial carcinoma (STIC) is a precursor lesion which is located in the distal fallopian tube and causes high grade serous ovarian carcinoma (HGSOC). The incidence of STIC for women underwent risk reducing salpingo-oophorectomy for BRCA mutation varies from 0.6 to 7% and its clinical outcomes are still unclear. The aim of this study was to demonstrate the incidence of STIC and HGSOC in BRCA1/2 mutation carriers after risk reducing salpingo-oophorectomy (RRSO) and the clinical outcomes of these patients. Material and methods: We retrospectively reviewed the records of 48 BRCA1 and/or 2 mutation carriers who underwent prophylactic salpingo-oophorectomy with or without hysterectomy at the Department of Obstetrics and Gynecology, Bursa Uludag University between January 2000 and January 2022. Inclusion criteria: BRCA 1 and/or 2 mutation carriers diagnosed by genetic testing, asymptomatic patients with no abnormal findings on pelvic examination. Exclusion criteria: patients with no abnormal findings on pelvic examination and a presence of a personal history of ovarian, fallopian tube or peritoneal cancer. Results: A total of 48 BRCA 1 and/or 2 mutation carriers underwent RRSO. STIC was diagnosed in 1 (2,0%) patient and restaging surgery was not performed. Primary peritoneal carcinoma (PPC) did not develop during the 20 months follow-up period. One (2.0%) patient was diagnosed with occult ovarian cancer. Restaging surgery was performed and chemotherapy treatments were given after surgery. A pelvic recurrence developed 25 months after the occult cancer diagnosis in the follow up period. One (2.0%) patient with normal histopathological findings after RRSO was diagnosed with peritoneal cancer 57 months after the operation. Conclusion: The risk of PPC continues after RRSO. Therefore, close follow-up procedure is very important for early diagnosis and effective treatment of patients with PPC after RRSO.
dc.identifier.doi10.1016/j.jogoh.2023.102642
dc.identifier.issn2468-7847
dc.identifier.issn1773-0430
dc.identifier.issue8
dc.identifier.pubmed37573025
dc.identifier.urihttps://doi.org/10.1016/j.jogoh.2023.102642
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S2468784723001095
dc.identifier.urihttps://hdl.handle.net/11452/42183
dc.identifier.volume52
dc.identifier.wos001058557100001
dc.indexed.wosWOS.SCI
dc.language.isoen
dc.publisherElsevier
dc.relation.journalJournal of Gynecology Obstetrics And Human Reproduction
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectFollow-up
dc.subjectCancer
dc.subjectCarriers
dc.subjectOvarian
dc.subjectOutcomes
dc.subjectSurgery
dc.subjectBrca 1/2
dc.subjectOvarian carcinoma
dc.subjectSerous tubal intraepithelial carcinoma
dc.subjectRisk reducing salpingo-oophorectomy
dc.subjectScience & technology
dc.subjectLife sciences & biomedicine
dc.subjectObstetrics & gynecology
dc.titleClinical significance of risk-reducing salpingo-oophorectomy in patients with BRCA1/2 mutation
dc.typeArticle
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Kadın Hastalıkları ve Doğum Ana Bilim Dalı
local.indexed.atPubMed
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relation.isAuthorOfPublication47fb1174-c9d0-40fc-bb18-53e5b1eb1df2
relation.isAuthorOfPublication.latestForDiscovery09b69994-b256-4bb6-9bbc-54981c10aee2

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