Incidence of ovarian cancer after bilateral salpingo-oophorectomy in women with histologically proven endometriosis.


Journal

Fertility and sterility
ISSN: 1556-5653
Titre abrégé: Fertil Steril
Pays: United States
ID NLM: 0372772

Informations de publication

Date de publication:
05 2022
Historique:
received: 27 09 2021
revised: 16 01 2022
accepted: 25 01 2022
pubmed: 19 3 2022
medline: 10 5 2022
entrez: 18 3 2022
Statut: ppublish

Résumé

To assess the incidence of ovarian cancer in women with histologically proven endometriosis after bilateral salpingo-oophorectomy (BSO). Retrospective nationwide cohort study. Dutch pathology database. Women with histologically proven endometriosis who had undergone BSO between 1990 and 2015 (n = 7,984). This study consists of 2 control cohorts: women with histologically proven endometriosis without BSO (n = 42,633) and women with a benign dermal nevus (n = 132,535). Observational study. Number of histologic diagnoses of (extra-)ovarian cancers. Incidence rate ratios (IRR) were estimated for (extra-)ovarian cancer. The number needed to treat was calculated. We identified 9 (0.1%) (extra-)ovarian cancers in the BSO cohort and 170 (0.4%) and 444 (0.3%) ovarian cancers in the endometriosis and nevus control cohorts, respectively. We found an age-adjusted IRR of 0.34 (95% confidence interval [CI], 0.15-0.76) when the BSO cohort was compared with the endometriosis cohort. Comparing the BSO cohort with the nevus control cohort resulted in an age-adjusted IRR of 0.38 (95% CI, 0.17-0.85). The number needed to treat when the BSO cohort was compared with the endometriosis control cohort was 351 (95% CI, 272-591). In this nationwide study, we found that the (extra-)ovarian cancer incidence in women with histologically proven endometriosis decreased to less than the background population risk after BSO. Additionally, we found a significant reduction of the incidence of ovarian cancer when compared with women with histologically proven endometriosis without BSO. Endometriosis surgery could in the future be a preventive strategy in women with endometriosis and a high-risk profile for ovarian cancer.

Identifiants

pubmed: 35300832
pii: S0015-0282(22)00065-6
doi: 10.1016/j.fertnstert.2022.01.030
pii:
doi:

Types de publication

Journal Article Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

938-945

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2022 American Society for Reproductive Medicine. Published by Elsevier Inc. All rights reserved.

Auteurs

Marjolein Hermens (M)

Department of Obstetrics and Gynecology, Catharina Hospital, Eindhoven, the Netherlands; Department of Obstetrics & Gynecology, Radboud University Medical Center, Nijmegen, the Netherlands. Electronic address: marjolein.hermens@catharinaziekenhuis.nl.

Anne M van Altena (AM)

Department of Obstetrics & Gynecology, Radboud University Medical Center, Nijmegen, the Netherlands.

Johan Bulten (J)

Department of Pathology, Radboud University Medical Center, Nijmegen, the Netherlands.

Huib A A M van Vliet (HAAM)

Department of Obstetrics and Gynecology, Catharina Hospital, Eindhoven, the Netherlands; Department of Obstetrics and Gynecology, University Hospital Ghent, Ghent, Belgium.

Albert G Siebers (AG)

Dutch Nationwide Registry of Histopathology and Cytopathology-Pathologisch Anatomisch Landelijk Geautomatiseerd Archief (PALGA), Houten, the Netherlands.

Ruud L M Bekkers (RLM)

Department of Obstetrics and Gynecology, Catharina Hospital, Eindhoven, the Netherlands; GROW School for Oncology and Developmental Biology, Maastricht University Medical Center, Maastricht, the Netherlands.

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