Evidence map›Paper›PMID 41346086›Full record

SynthesisUltrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology2026

Diagnostic accuracy of ultrasound models for assessment of ovarian tumors: systematic review and meta-analysis.

E Lems, A H Koch, E J L G Delvaux, J C Leemans, M Y Bongers, C A R Lok, B L Ramaekers, P M A J Geomini

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

8 authors.

E LemsDepartment of Obstetrics and Gynaecology, Máxima Medical Center, Veldhoven, The Netherlands.ORCID 0000-0002-4495-9622
A H KochDepartment of Gynaecologic Oncology, Center of Gynaecologic Oncology Amsterdam, location Antoni van Leeuwenhoek, Netherlands Cancer Institute, Amsterdam, The Netherlands.
E J L G DelvauxDepartment of Research and Medical Innovation, Máxima Medical Center, Veldhoven, The Netherlands.
J C LeemansDepartment of Obstetrics and Gynaecology, Máxima Medical Center, Veldhoven, The Netherlands.
M Y BongersDepartment of Obstetrics and Gynaecology, Máxima Medical Center, Veldhoven, The Netherlands.
C A R LokDepartment of Gynaecologic Oncology, Center of Gynaecologic Oncology Amsterdam, location Antoni van Leeuwenhoek, Netherlands Cancer Institute, Amsterdam, The Netherlands.
B L RamaekersDepartment of Clinical Epidemiology and Medical Technology Assessment, Maastricht University, Maastricht, The Netherlands.
P M A J GeominiDepartment of Obstetrics and Gynaecology, Máxima Medical Center, Veldhoven, The Netherlands.

Funding

ZonMw 852002128
6 · The paper itself

Abstract

objectiveAccurate preoperative classification of ovarian tumors is essential for guiding treatment. There is an increasing body of data evaluating ultrasound-based models for this purpose in diverse clinical settings. The aim of this systematic review and meta-analysis was to generate up-to-date evidence on the diagnostic accuracy of the most relevant ultrasound-based models, including the Risk of Malignancy Index (RMI) versions 1, 2 and 3, Logistic Regression model 2 (LR2), Simple ultrasound-based Rules (SR), the Assessment of Different NEoplasias in the adneXa (ADNEX) model and subjective assessment (SA), for the differentiation between benign and malignant ovarian tumors.

methodsOvid/MEDLINE, EMBASE and the Cochrane Library were searched systematically from database inception until 19 June 2025. Eligible studies investigated the diagnostic accuracy of at least one of the preselected models, collected model parameters prospectively and provided sufficient data to construct 2 × 2 tables. The risk of bias of all included studies was assessed using the Quality Assessment of Diagnostic Accuracy Studies (QUADAS)-2 and QUADAS-C extension tools. Pooled summary estimates of sensitivity and specificity for all included models were calculated and bivariate models were fitted into hierarchical summary receiver-operating-characteristics curves. Bivariate random-effects meta-regression analysis was conducted to determine significant differences in sensitivity and specificity between models. Subgroup analyses were conducted according to menopausal status and prevalence of ovarian malignancy.

resultsA total of 99 studies were included, describing 42 496 ovarian tumors, of which 31 371 (74%) were benign and 11 125 (26%) were malignant. SA had both high sensitivity (90.2% (95% CI, 87.8-92.2%)) and high specificity (91.4% (95% CI, 89.3-93.2%)). SR followed by SA of inconclusive cases (SR + SA) showed similar performance to SA (sensitivity, 88.6% (95% CI, 85.7-91.0%); P = 0.397 and specificity, 91.0% (95% CI, 89.0-92.7%); P = 0.811), as did the ADNEX model with a cut-off of 20% (sensitivity, 86.7% (95% CI, 80.6-91.0%); P = 0.095; specificity, 87.9% (95% CI, 80.1-92.9%), P = 0.119). The ADNEX model with a cut-off of 10% had a similar sensitivity to SA (92.7% (95% CI, 90.8-94.2%); P = 0.130), but lower specificity (78.4% (95% CI, 71.7-83.8%); P < 0.001). Higher cut-offs of the ADNEX model led to a decrease in sensitivity, whereas lower cut-offs resulted in reduced specificity. The LR2 model with a 10% cut-off had a sensitivity of 89.5% (95% CI, 85.8-92.4%) and a specificity of 82.3% (95% CI, 75.0-87.8%). The RMI had the lowest diagnostic accuracy, with a sensitivity of 69.7% (95% CI, 67.0-72.2%) and a specificity of 90.5% (95% CI, 88.3-92.4%) for RMI version 1 with a cut-off of 200. Subgroup analyses showed that both menopausal status and prevalence of malignancy significantly affected sensitivity (P < 0.01) and specificity (P < 0.01). Postmenopausal status and higher disease prevalence were associated with lower specificity, while sensitivity was lower in premenopausal women.

conclusionsAll approaches, except for the RMI, performed well and could be used to differentiate between benign and malignant ovarian tumors. Although SA with or without SR had the highest diagnostic performance, it is dependent on operator expertise. If a strategy independent of operator expertise is preferred, the ADNEX model is recommended. Because of the high sensitivity of the ADNEX model, the likelihood of missing malignancies is low. In postmenopausal women, however, the reduced specificity may warrant a higher cut-off, depending on how the impact of a false-positive test result is evaluated. © 2025 The Author(s). Ultrasound in Obstetrics & Gynecology published by John Wiley & Sons Ltd on behalf of International Society of Ultrasound in Obstetrics and Gynecology.

Indexed as

Ovarian NeoplasmsDiagnosis, DifferentialFemaleHumansSensitivity and SpecificityUltrasonographymeta‐analysisovarian cancerrisk assessmentultrasound

Identifiers

PMID41346086
PMCPMC13136063

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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.