Evidence map›Paper›PMID 41906961›Full record

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

Developing and validating ultrasound-based machine-learning models incorporating radiomics features to predict malignancy in adnexal masses.

F Moro, M Ciancia, S di Berardino, G Baldassari, F Mascilini, F Ciccarone, C Nero, H E Tran, T Pasciuto, L Boldrini and 8 more

Abstract readObservational StudyValidation Study
In one paragraph

Observational study 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. 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

18 authors.

F MoroUniCamillus-International Medical University of Rome, Rome, Italy.ORCID 0000-0002-5070-7245
M CianciaDipartimento Scienze della Salute della Donna e del Bambino, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.ORCID 0009-0001-9443-1834
S di BerardinoDipartimento Scienze della Salute della Donna e del Bambino, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.
G BaldassariRadiomics G-STeP Research Core Facility, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.ORCID 0000-0001-8172-1093
F MasciliniDipartimento Scienze della Salute della Donna e del Bambino, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.ORCID 0000-0003-0736-3114
F CiccaroneDipartimento Scienze della Salute della Donna e del Bambino, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.ORCID 0000-0003-2104-0602
C NeroDipartimento Scienze della Salute della Donna e del Bambino, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.ORCID 0000-0002-4442-4046
H E TranRadiomics G-STeP Research Core Facility, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.ORCID 0000-0002-7176-9090
T PasciutoData Collection G-STeP Research Core Facility, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
L BoldriniRadiomics G-STeP Research Core Facility, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.
D GiannarelliEpidemiology and Biostatistics Facility, G-STeP Generator, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
A LedgerDepartment of Development and Regeneration, KU Leuven, Leuven, Belgium.
T BourneDepartment of Development and Regeneration, KU Leuven, Leuven, Belgium.ORCID 0000-0003-1421-6059
W FroymanDepartment of Development and Regeneration, KU Leuven, Leuven, Belgium.ORCID 0000-0002-1398-9124
D TimmermanDepartment of Development and Regeneration, KU Leuven, Leuven, Belgium.ORCID 0000-0002-3707-6645
L ValentinDepartment of Obstetrics and Gynaecology, Skåne University Hospital, Malmö, Sweden.ORCID 0000-0002-3830-6414
A FagottiDipartimento Scienze della Salute della Donna e del Bambino, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.
A C TestaDipartimento Scienze della Salute della Donna e del Bambino, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe primary aim of this study was to develop and internally validate ultrasound-based radiomics models to discriminate between all types of benign and malignant adnexal masses. The secondary aim was to compare the performance of the radiomics models with that of the Assessment of Different NEoplasias in the adneXa (ADNEX) model.

methodsThis was a retrospective, observational, single-center study, for which all patients with an adnexal mass that were included in the ongoing International Ovarian Tumor Analysis phase-5 and phase-7 studies and were examined using ultrasound between January 2012 and December 2023 at Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy, were eligible for inclusion. Inclusion criteria were: adnexal mass detected by ultrasound; surgical removal of the adnexal mass within 180 days after the ultrasound examination; histological confirmation of an adnexal mass; and absence of a synchronous malignant tumor. Patients without digital ultrasound images saved in DICOM format were excluded. The patient cohort was split randomly into training and validation sets using a stratified split with a ratio of 70:30, to preserve the proportion of benign and malignant cases in the two sets. Two machine-learning models for discriminating between benign and malignant adnexal masses were built using one image per tumor, with 5-fold cross-validation for hyperparameter tuning, and were tested on the validation set. The variables used in model building were patient age, serum CA 125 level and the radiomics features that differed significantly between benign and malignant tumors (determined using the Mann-Whitney U-test with Benjamini-Hochberg correction) and were not redundant based on Pearson correlation analysis. Histology was the reference standard. We assessed the discriminative performance of the radiomics models using the area under the receiver-operating-characteristics curve (AUC) and classification performance using sensitivity and specificity at the optimal cut-off of each model to classify the mass as malignant, as determined by Youden's index. The diagnostic performance of the developed radiomics models was compared with that of the ADNEX model (AUC, sensitivity and specificity at the 10% risk-of-malignancy cut-off, which is the recommended threshold for clinical use of the ADNEX model).

resultsIn total, 4501 patients met the inclusion criteria. Among these, 2428 patients were excluded owing to an absence of ultrasound images or images unsuitable for radiomics analysis. Overall, a total of 2073 patients were included in the analysis, of whom 803 (38.7%) had a histologically confirmed malignant tumor. In the validation set (n = 622, including 254 malignancies), the clinical-radiomics model trained using the eXtreme Gradient Boosting algorithm, including age, serum CA 125 level and 14 selected radiomics features, achieved the highest performance, with an AUC of 0.89 (95% CI, 0.86-0.92), sensitivity of 0.83 (95% CI, 0.79-0.88) and specificity of 0.81 (95% CI, 0.77-0.85) at the optimal cut-off (31% risk of malignancy, based on Youden's index). At a 10% risk-of-malignancy cut-off, it had a sensitivity of 0.94 (95% CI, 0.91-0.97) and specificity of 0.48 (95% CI, 0.42-0.53). The ADNEX model had an AUC of 0.95 (95% CI, 0.93-0.97), sensitivity of 0.97 (95% CI, 0.95-0.99) and specificity of 0.72 (95% CI, 0.68-0.77) at the 10% risk-of-malignancy cut-off in the validation set.

conclusionsOur results support further exploration of radiomics analysis for distinguishing between benign and malignant adnexal masses in larger study populations. Future studies should consider using multiple images per tumor and testing alternative model-building methods, and should perform external validation to assess the generalizability of the radiomics models. © 2026 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

Adnexal DiseasesMachine LearningOvarian NeoplasmsAdultAgedFemaleHumansMiddle AgedPredictive Value of TestsRadiomicsRetrospective StudiesROC CurveSensitivity and SpecificityUltrasonographyAIartificial intelligencemachine learningovarian massesradiomicsultrasonography

Identifiers

PMID41906961
PMCPMC13040134

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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.