AI Article Synopsis

  • This study compares two diagnostic models, ADNEX and ROMA, used to identify whether adnexal masses (tumors near the ovaries) are benign or malignant.
  • The research included 894 women undergoing surgery for adnexal tumors and found that ADNEX outperformed ROMA in terms of accuracy, particularly when combined with the biomarker CA125.
  • The results indicate that ADNEX not only provided better discrimination between tumor types but also had greater clinical utility, making it a more effective tool for clinicians in practice.

Article Abstract

Background: Several diagnostic prediction models to help clinicians discriminate between benign and malignant adnexal masses are available. This study is a head-to-head comparison of the performance of the Assessment of Different NEoplasias in the adneXa (ADNEX) model with that of the Risk of Ovarian Malignancy Algorithm (ROMA).

Methods: This is a retrospective study based on prospectively included consecutive women with an adnexal tumour scheduled for surgery at five oncology centres and one non-oncology centre in four countries between 2015 and 2019. The reference standard was histology. Model performance for ADNEX and ROMA was evaluated regarding discrimination, calibration, and clinical utility.

Results: The primary analysis included 894 patients, of whom 434 (49%) had a malignant tumour. The area under the receiver operating characteristic curve (AUC) was 0.92 (95% CI 0.88-0.95) for ADNEX with CA125, 0.90 (0.84-0.94) for ADNEX without CA125, and 0.85 (0.80-0.89) for ROMA. ROMA, and to a lesser extent ADNEX, underestimated the risk of malignancy. Clinical utility was highest for ADNEX. ROMA had no clinical utility at decision thresholds <27%.

Conclusions: ADNEX had better ability to discriminate between benign and malignant adnexal tumours and higher clinical utility than ROMA.

Clinical Trial Registration: clinicaltrials.gov NCT01698632 and NCT02847832.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10951363PMC
http://dx.doi.org/10.1038/s41416-024-02578-xDOI Listing

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