Evidence map›Paper›PMID 41442084›Full record

Observational studyCancer causes & control : CCC2025

Clinical value of serum biomarkers, magnetic resonance imaging risk scoring, and malignancy risk indices in distinguishing benign and malignant ovarian masses: an observational study.

Naina Kumar, Mishu Mangla, Subhrajyoti Roy, Aparna Setty, Srujana Veldi, Pooja T Rathod

Abstract readObservational Study
PubMed Publisher
In one paragraph

Observational study in Cancer causes & control : CCC, 2025. 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

6 authors.

Naina KumarDepartment of Obstetrics and Gynaecology, All India Institute of Medical Sciences, Bibinagar, Hyderabad Metropolitan Region, Hyderabad, Telangana, 508126, India. drnainakumar@gmail.com.ORCID http://orcid.org/0000-0002-5970-6935
Mishu ManglaDepartment of Obstetrics and Gynaecology, All India Institute of Medical Sciences, Bibinagar, Hyderabad Metropolitan Region, Hyderabad, Telangana, 508126, India.
Subhrajyoti RoyDepartment of Obstetrics and Gynaecology, All India Institute of Medical Sciences, Bibinagar, Hyderabad Metropolitan Region, Hyderabad, Telangana, 508126, India.
Aparna SettyDepartment of Obstetrics and Gynaecology, All India Institute of Medical Sciences, Bibinagar, Hyderabad Metropolitan Region, Hyderabad, Telangana, 508126, India.
Srujana VeldiDepartment of Obstetrics and Gynaecology, All India Institute of Medical Sciences, Bibinagar, Hyderabad Metropolitan Region, Hyderabad, Telangana, 508126, India.
Pooja T RathodDepartment of Obstetrics and Gynaecology, All India Institute of Medical Sciences, Bibinagar, Hyderabad Metropolitan Region, Hyderabad, Telangana, 508126, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeAccurate preoperative differentiation between benign and malignant adnexal masses is essential for guiding optimal surgical management. This study aimed to assess the diagnostic performance, calibration, and clinical utility of serum biomarkers (CA-125, CEA), the O-RADS MRI risk score, and Risk of Malignancy Indices (RMI-I-V) in both premenopausal and postmenopausal women.

methodsThis retrospective study included data from consecutive patients who underwent surgical management for ovarian masses at a rural tertiary care center in Southern India over 2 years. Preoperative ultrasonography, serum CA-125, CEA levels, and O-RADS MRI risk scores were recorded. RMI-I-V were calculated for each case. Statistical analyses included Receiver Operating Characteristic (ROC) curves, calibration plots, and decision curve analysis to assess discrimination and clinical utility across decision thresholds (5-50%).

resultsA total of 129 women were evaluated-98 (75.9%) had benign, 5 (3.9%) borderline, and 26 (20.2%) malignant ovarian masses. At recommended cut-offs, all RMI models and serum biomarkers significantly differentiated between benign, borderline, and malignant cases. RMI-IV and RMI-V demonstrated the best sensitivity (92.31%), specificity (90.82% and 92.86%), and negative predictive values (97.80% and 97.85%), whereas CEA showed the poorest sensitivity (23.08%). Calibration was most accurate for RMI-V, with RMI-II and RMI-IV also performing well. Decision curve analysis confirmed the highest net clinical benefit for RMI-II and RMI-IV across thresholds of 5-50%.

conclusionRMI-based models, especially RMI-IV, demonstrated excellent diagnostic accuracy and clinical utility, supporting their use as a reliable, cost-effective tool for adnexal mass evaluation.

Indexed as

Biomarkers, TumorMagnetic Resonance ImagingOvarian NeoplasmsAdultAgedCA-125 AntigenDiagnosis, DifferentialFemaleHumansMiddle AgedRetrospective StudiesROC CurveYoung AdultBiomarkers, TumorCA-125 AntigenArea under the curveBenignMalignantOvaryRisk of malignancy index

Identifiers

PMID41442084

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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.