Evidence map›Paper›PMID 41955317›Full record

ArticleJournal of the National Cancer Institute2026

Menopause-related quality of life 5 years after salpingectomy with delayed oophorectomy vs salpingo-oophorectomy.

Tamar A Gootzen, Rosella P M G Hermens, Marleen M H J van Gelder, Elle Heijnen, Majke H D van Bommel, Mirjam J A Apperloo, Monique M A Brood-van Zanten, Sjors F P J Coppus, Jose A E Custers, Helena C van Doorn and 16 more

Abstract readComparative Study
In one paragraph

Article in Journal of the National Cancer Institute, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

26 authors.

Tamar A GootzenDepartment of Gynaecology and Obstetrics, Radboudumc, Nijmegen, The Netherlands.ORCID 0009-0005-8916-1568
Rosella P M G HermensIQ Health, Radboudumc, Nijmegen, The Netherlands.ORCID 0000-0001-7624-7120
Marleen M H J van GelderIQ Health, Radboudumc, Nijmegen, The Netherlands.ORCID 0000-0003-4853-4434
Elle HeijnenDepartment of Gynaecology and Obstetrics, Radboudumc, Nijmegen, The Netherlands.ORCID 0009-0006-8782-9365
Majke H D van BommelDepartment of Gynaecology and Obstetrics, Radboudumc, Nijmegen, The Netherlands.ORCID 0000-0002-7562-9861
Mirjam J A ApperlooDepartment of Obstetrics and Gynecology, Frisius MC, Leeuwarden, The Netherlands.
Monique M A Brood-van ZantenDepartment of Gynecology, Netherlands Cancer Institute/Antoni van Leeuwenhoek, Amsterdam, The Netherlands.
Sjors F P J CoppusDepartment of Obstetrics and Gynecology, Maxima Medical Centre, Veldhoven, The Netherlands.ORCID 0000-0001-6786-5824
Jose A E CustersDepartment of Medical Psychology, Radboudumc, Nijmegen, The Netherlands.
Helena C van DoornDepartment of Gynecology, Erasmus MC Cancer Clinic, Rotterdam, The Netherlands.ORCID 0000-0003-1062-4485
Katja N GaarenstroomDepartment of Obstetrics and Gynecology, Leiden University Medical Centre, Leiden, The Netherlands.ORCID 0000-0002-4702-1680
Marline G HarmsenDepartment of Gynaecology and Obstetrics, Radboudumc, Nijmegen, The Netherlands.
Joanna IntHoutIQ Health, Radboudumc, Nijmegen, The Netherlands.ORCID 0000-0002-6127-0747
Marjan KnippenbergIQ Health, Radboudumc, Nijmegen, The Netherlands.ORCID 0000-0001-9707-7458
Luc R C W van LonkhuijzenCenter for Gynecologic Oncology, Cancer Center Amsterdam UMC, Amsterdam, The Netherlands.ORCID 0000-0001-6905-2704
Marian J E MouritsDepartment of Obstetrics and Gynecology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.ORCID 0000-0003-2385-2639
Jurgen M J PiekDepartment of Gynaecology and Obstetrics and Catharina Cancer Institute, Catharina Hospital, Eindhoven, The Netherlands.ORCID 0000-0002-0487-0631
Teska N SchuurmanDepartment of Gynaecology, Netherlands Cancer Institute, Antoni van Leeuwenhoek, Amsterdam, The Netherlands.
Michiel SimonsDepartment of Pathology, Radboudumc, Nijmegen, The Netherlands.ORCID 0000-0003-1039-3488
Brigitte F M SlangenDepartment of Obstetrics and Gynecology, Maastricht University Medical Centre, GROW-School for Oncology and Developmental Biology, Maastricht, The Netherlands.ORCID 0000-0003-2811-3851
Rachel TrosCenter for Gynecologic Oncology, Cancer Center Amsterdam UMC, Amsterdam, The Netherlands.ORCID 0000-0003-4070-2018
M Caroline VosDepartment of Obstetrics and Gynaecology, Elisabeth-TweeSteden Hospital, Tilburg, The Netherlands.ORCID 0000-0002-1612-0395
Ronald P ZweemerDepartment of Gynecological Oncology, UMC Utrecht, Utrecht, The Netherlands.ORCID 0000-0003-1829-7773
C Marleen KetsDepartment of Human Genetics, Radboudumc, Nijmegen, The Netherlands.
Joanne de HulluDepartment of Gynaecology and Obstetrics, Radboudumc, Nijmegen, The Netherlands.
Miranda P SteenbeekDepartment of Gynaecology and Obstetrics, Radboudumc, Nijmegen, The Netherlands.

Funding

Dutch Cancer Society KUN2014-7187
6 · The paper itself

Abstract

backgroundBRCA1/2 pathogenic variant (PV) carriers have an increased risk of tubo-ovarian cancer. They are recommended to have a risk-reducing salpingo-oophorectomy around age 40, resulting in premature menopause. The alternative risk-reducing salpingectomy (RRS) with delayed oophorectomy (DO) postpones this. We present the 5-year results of a nationwide preference trial (TUBA study) comparing menopause-related quality of life (QoL) after RRS/DO with salpingo-oophorectomy.

methodsPremenopausal BRCA1/2-PV carriers aged 25-40 (BRCA1) or 25-45 (BRCA2) chose RRS/DO or salpingo-oophorectomy with or without hormonal replacement therapy (HRT). We compared QoL (Greene Climacteric Scale) between RRS/DO and salpingo-oophorectomy without HRT 5 years after surgery using linear mixed models. Secondarily, RRS/DO was compared with salpingo-oophorectomy with HRT. Women who underwent oophorectomy in the RRS/DO group were excluded in a sensitivity analysis.

resultsIn total, 410 (71.9%) participants chose RRS/DO and 160 (28.1%) salpingo-oophorectomy. Seventy-three (17.8%) participants underwent oophorectomy within 5 years after salpingectomy. The adjusted mean difference (aMD) in QoL was 1.8 (95% CI = -0.6 to 4.3) after salpingo-oophorectomy without HRT and 1.4 (95% CI = -0.4 to 3.1) after salpingo-oophorectomy with HRT compared with RRS (with and without oophorectomy) at 5 years follow-up. The sensitivity analysis showed that QoL decreased less after RRS before oophorectomy compared with salpingo-oophorectomy without (aMD = 2.4, 95% CI = 0.1 to 4.8) and with HRT (aMD = 1.9, 95% CI = 0.1 to 3.7).

conclusionPostponing oophorectomy is key in preventing deterioration of QoL. QoL was similar 5 years after salpingectomy (with and without oophorectomy) compared with salpingo-oophorectomy (regardless of HRT use). However, QoL was higher when comparing salpingectomy without oophorectomy to salpingo-oophorectomy (regardless of HRT use).

Indexed as

Fallopian Tube NeoplasmsMenopauseOvarian NeoplasmsOvariectomyQuality of LifeSalpingectomySalpingo-oophorectomyAdultBRCA1 ProteinBRCA2 ProteinFemaleHumansMiddle AgedBRCA1 ProteinBRCA1 protein, humanBRCA2 ProteinBRCA2 protein, human

Identifiers

PMID41955317
PMCPMC13549723

What Socratic holds

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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 Socratic graph.