Evidence map›Paper›PMID 39823150›Full record

ArticleBJOG : an international journal of obstetrics and gynaecology2025

Salpingectomy With Delayed Oophorectomy Versus Salpingo-Oophorectomy in BRCA1/2 Carriers: Three-Year Outcomes of a Prospective Preference Trial.

Majke H D Van Bommel, Miranda P Steenbeek, Joanna Inthout, Tessa Van Garderen, Marline G Harmsen, Marieke Arts-De Jong, Angela H E M Maas, Judith B Prins, Johan Bulten, Helena C Van Doorn and 14 more

Abstract readMulticenter StudyComparative Study
In one paragraph

Article in BJOG : an international journal of obstetrics and gynaecology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Article
  2. Further Considerations on Risk-Reducing Salpingectomy and Oophorectomy in BRCA1/2 Carriers.BJOG : an international journal of obstetrics and gynaecology · 2026
    Article
  3. Contemporary risk assessment and risk-reducing strategies for tubo-ovarian cancer in women with BRCA pathogenic variants.International journal of gynecological cancer : official journal of the International Gynecological Cancer Society · 2026
    Review
  4. Review
  5. Article
  6. Review
  7. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

24 authors.

Majke H D Van BommelRadboud University Medical Center, Radboud Institute for Health Sciences, Department of Obstetrics and Gynecology, Nijmegen, The Netherlands.ORCID https://orcid.org/0000-0002-7562-9861
Miranda P SteenbeekRadboud University Medical Center, Radboud Institute for Health Sciences, Department of Obstetrics and Gynecology, Nijmegen, The Netherlands.
Joanna InthoutDepartment for Health Evidence, Radboud University Medical Center, Nijmegen, The Netherlands.
Tessa Van GarderenRadboud University Medical Center, Radboud Institute for Health Sciences, Department of Obstetrics and Gynecology, Nijmegen, The Netherlands.
Marline G HarmsenRadboud University Medical Center, Radboud Institute for Health Sciences, Department of Obstetrics and Gynecology, Nijmegen, The Netherlands.
Marieke Arts-De JongRadboud University Medical Center, Radboud Institute for Health Sciences, Department of Obstetrics and Gynecology, Nijmegen, The Netherlands.
Angela H E M MaasDepartment of Cardiology, Radboud University Medical Center, Nijmegen, The Netherlands.
Judith B PrinsDepartment of Medical Psychology, Radboud University Medical Center, Nijmegen, The Netherlands.
Johan BultenDepartment of Pathology, Radboud University Medical Center, Nijmegen, The Netherlands.
Helena C Van DoornDepartment of Gynecology, Erasmus MC Cancer Clinic, Rotterdam, The Netherlands.ORCID https://orcid.org/0000-0003-1062-4485
Marian J E MouritsDepartment of Gynecologic Oncology, University of Groningen, University Medical Centre Groningen, Groningen, The Netherlands.
Rachel TrosVUmc, Department of Obstetrics and Gynecology, Amsterdam, The Netherlands.
Ronald P ZweemerDepartment of Gynecological Oncology, UMC Utrecht Cancer Centre, Utrecht, The Netherlands.
Katja N GaarenstroomDepartment of Obstetrics and Gynecology, Leiden University Medical Centre, Leiden, The Netherlands.
Brigitte F M SlangenDepartment of Obstetrics and Gynecology, Maastricht University Medical Centre, GROW-School for Oncology and Developmental Biology, Maastricht, The Netherlands.
Monique M A Brood-Van ZantenVUmc, Department of Obstetrics and Gynecology, Amsterdam, The Netherlands.
M Caroline VosGynecologic Oncologic Centre South Location Elisabeth-TweeSteden Hospital, Tilburg, The Netherlands.
Jurgen M J PiekGynecologic Oncologic Centre South Location Catharina Hospital, Eindhoven, The Netherlands.
Luc R C W van LonkhuijzenDepartment of Gynecology, Netherlands Cancer Institute/Antoni van Leeuwenhoek, Amsterdam, The Netherlands.
Mirjam J A ApperlooDepartment of Obstetrics and Gynecology, Medical Centre Leeuwarden, Leeuwarden, The Netherlands.
Sjors F P J CoppusDepartment of Obstetrics and Gynecology, Maxima Medical Centre, Veldhoven, The Netherlands.
Nicoline HoogerbruggeRadboud University Medical Center, Radboud Institute for Health Sciences, Department of Human Genetics, Nijmegen, The Netherlands.
Rosella P M G HermensRadboud University Medical Center, Scientific Institute for Quality of Healthcare, Nijmegen, The Netherlands.
Joanne A De HulluRadboud University Medical Center, Radboud Institute for Health Sciences, Department of Obstetrics and Gynecology, Nijmegen, The Netherlands.

Funding

Dutch Cancer Society KUN 2014-7187KWF Kankerbestrijding
6 · The paper itself

Abstract

objectiveTo compare menopause-related quality of life (QoL) after risk-reducing salpingectomy (RRS) versus risk-reducing salpingo-oophorectomy (RRSO) until 3 years of post-surgery.

designA prospective study (TUBA study) with treatment allocation based on patients' preference. Data were collected pre-surgery and at 3 months, 1 and 3 years of post-surgery.

settingMulticentre prospective preference trial in thirteen hospitals in the Netherlands. POPULATION: BRCA1/2 pathogenic variant (PV) carriers aged 25-40 (BRCA1) or 25-45 (BRCA2), who were premenopausal, without a future child wish and without current (treatment for) malignancy.

methodsTreatment allocation was based on patients' preference: either RRS from the age of 25 years with delayed oophorectomy at the maximum age of 45 (BRCA1) or 50 (BRCA2), or RRSO between the ages of 35-40 (BRCA1) or 40-45 (BRCA2). After RRSO, hormone replacement therapy (HRT) was recommended, if not contraindicated. Primarily, menopause-related QoL as measured with the Greene Climacteric Scale (GCS) was compared between the RRS and RRSO without HRT group. Secondarily, GSC-scores of the RRS group were compared with the scores of the RRSO with HRT after surgery group. A higher GSC-score reflects more climacteric symptoms.

resultsUntil April 2023, 410 participants had undergone RRS and 160 RRSO. The BRCA1/BRCA2 proportions were 51.4%/48.6%. The mean age at surgery (SD) was 37.9 (3.5) years. Participants 3 years after RRSO without HRT had a 4.3 (95% CI 2.1-6.5; p < 0.001) point higher increase in GCS-score from baseline compared to those after RRS, while the difference was 7.9 (95% CI 5.9-9.8) and 8.5 (95% CI 6.5-10.5) points at 3 and 12 months, respectively. Among participants with HRT after surgery, the RRSO group had a 2.4 (95% CI 0.8-3.9; p = 0.002) point higher increase in GCS-score from baseline compared to the RRS group.

conclusionsIn this multicentre preference trial, menopause-related QoL was better after RRS than after RRSO, even with HRT after RRSO. Differences between arms were most pronounced until one-year post-surgery.

Indexed as

Ovarian NeoplasmsOvariectomySalpingectomySalpingo-oophorectomyAdultBRCA1 ProteinBRCA2 ProteinFemaleGenes, BRCA1Genes, BRCA2HeterozygoteHumansMenopauseMiddle AgedNetherlandsPatient PreferenceBRCA1 ProteinBRCA1 protein, humanBRCA2 ProteinBRCA2 protein, humanBRCA1BRCA2delayed oophorectomyovarian cancerquality of lifesalpingectomysalpingo‐oophorectomy

Identifiers

PMID39823150
PMCPMC11969916

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.