External validation of ADNEX MR SCORING system: a single-centre retrospective study.


Journal

Clinical radiology
ISSN: 1365-229X
Titre abrégé: Clin Radiol
Pays: England
ID NLM: 1306016

Informations de publication

Date de publication:
02 2019
Historique:
received: 09 08 2018
accepted: 31 10 2018
pubmed: 6 12 2018
medline: 27 11 2019
entrez: 6 12 2018
Statut: ppublish

Résumé

To evaluate the accuracy of the ADNEX MR SCORING system for characterising adnexal masses. An institutional review board approved this retrospective study. The study population comprised 663 women who underwent magnetic resonance imaging (MRI) from January 2007 to December 2014 to characterise 778 adnexal masses that were indeterminate under ultrasonography (590 benign and 188 malignant). Two radiologists independently reviewed the MRI images. The masses were scored from 1 to 5 according to the ADNEX MR SCORING system. The diagnostic performance of the system was evaluated by receiver operating characteristic (ROC) analysis. Masses scored 4 or greater were considered malignant (including tumours of borderline malignancy or low malignant potential). The malignancy rates of masses with scores of 2, 3, 4 and 5 were 1.9% (8/419), 12.8% (19/149), 62.6% (57/91) and 87.4% (104/119) for reader 1 and 2.1% (9/424), 13.6% (20/147), 67.6% (71/105) and 86.3% (88/102) for reader 2, respectively. The areas under the ROC curves for the differentiation of benign and malignant masses were 0.929 and 0.923, respectively; the sensitivity, specificity and accuracy of diagnosis were 85.6% (161/188), 91.7% (541/590), and 90.2% (702/778) for reader 1 and 84.6% (159/188), 91.9% (542/590), and 90.1% (701/778) for reader 2, respectively. Tumours of borderline malignancy or low malignant potential had a higher rate of misclassification (46.1%) than other malignant tumours (6-7.4%). The ADNEX MR SCORING system was highly accurate in differentiating benign and malignant adnexal masses, although it may be less accurate for tumours of borderline malignancy or low malignant potential.

Identifiants

pubmed: 30514585
pii: S0009-9260(18)30584-1
doi: 10.1016/j.crad.2018.10.014
pii:
doi:

Types de publication

Journal Article Validation Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

131-139

Informations de copyright

Copyright © 2018 The Royal College of Radiologists. Published by Elsevier Ltd. All rights reserved.

Auteurs

K Sasaguri (K)

Department of Radiology, Faculty of Medicine, Saga University, Saga, 849-8501, Japan. Electronic address: k.sasaguri@gmail.com.

K Yamaguchi (K)

Department of Radiology, Faculty of Medicine, Saga University, Saga, 849-8501, Japan.

T Nakazono (T)

Department of Radiology, Faculty of Medicine, Saga University, Saga, 849-8501, Japan.

M Mizuguchi (M)

Department of Radiology, Faculty of Medicine, Saga University, Saga, 849-8501, Japan.

S Aishima (S)

Department of Pathology and Microbiology, Faculty of Medicine, Saga University, Saga, 849-8501, Japan.

M Yokoyama (M)

Department of Obstetrics & Gynecology, Faculty of Medicine, Saga University, Saga, 849-8501, Japan.

H Irie (H)

Department of Radiology, Faculty of Medicine, Saga University, Saga, 849-8501, Japan.

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