Evaluation of the Clinical Performance of the cobas 4800 HPV Test in Patients Referred for Colposcopy

Author:

White Christine12,Keegan Helen12,Pilkington Loretto2,Ruttle Carmel2,Kerr Patrick2,Sharp Linda3,O'Toole Sharon1,Turner Michael4,Prendiville Walter4,D'Arcy Tom4,Fitzpatrick Myra5,Lenehan Peter5,Flannelly Grainne5,O'Leary John J.12,Martin Cara M.12

Affiliation:

1. Department of Histopathology, Trinity College Dublin, Dublin, Ireland

2. Department of Pathology, Coombe Women's and Infants University Hospital, Dublin, Ireland

3. National Cancer Registry Ireland, Cork, Ireland

4. Department of Obstetrics and Gynaecology, Coombe Women and Infants University Hospital, Dublin, Ireland

5. Department of Obstetrics and Gynaecology, National Maternity Hospital, Dublin, Ireland

Abstract

ABSTRACT The clinical performance of the cobas human papillomavirus (HPV) test for detection of high-grade disease in a colposcopy-referred population was compared with that of Hybrid Capture 2 (HC2). The overall agreement between the tests was 92.3%. Clinical sensitivity and specificity for detection of cervical intraepithelial neoplasia grade 2 or greater (CIN2+) were 90.0% and 55.5% for cobas and 90.5% and 50.2% for HC2, respectively. In conclusion, both tests showed comparable performance for detection of CIN2+.

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

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