TY - JOUR
T1 - Comparison of the ADNEX and ROMA risk prediction models for the diagnosis of ovarian cancer
T2 - a multicentre external validation in patients who underwent surgery
AU - Landolfo, Chiara
AU - Ceusters, Jolien
AU - Valentin, Lil
AU - Froyman, Wouter
AU - Van Gorp, Toon
AU - Heremans, Ruben
AU - Baert, Thaïs
AU - Wouters, Roxanne
AU - Vankerckhoven, Ann
AU - Van Rompuy, Anne Sophie
AU - Billen, Jaak
AU - Moro, Francesca
AU - Mascilini, Floriana
AU - Neumann, Adam
AU - Van Holsbeke, Caroline
AU - Chiappa, Valentina
AU - Bourne, Tom
AU - Fischerova, Daniela
AU - Testa, Antonia
AU - Coosemans, An
AU - Timmerman, Dirk
AU - Van Calster, Ben
PY - 2024
Y1 - 2024
N2 - 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.
AB - 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.
U2 - 10.1038/s41416-024-02578-x
DO - 10.1038/s41416-024-02578-x
M3 - Article
C2 - 38243011
AN - SCOPUS:85182629437
SN - 0007-0920
VL - 130
SP - 934
EP - 940
JO - British Journal of Cancer
JF - British Journal of Cancer
IS - 6
ER -