Longitudinal Clinical Performance of the RNA-Based Aptima Human Papillomavirus (AHPV) Assay in Comparison to the DNA-Based Hybrid Capture 2 HPV Test in Two Consecutive Screening Rounds with a 6-Year Interval in Germany

Author:

Iftner Thomas1,Neis Klaus-Joachim2,Castanon Alejandra34,Landy Rebecca3,Holz Barbara1,Woll-Herrmann Astrid2,Iftner Angelika1,Staebler Annette5,Wallwiener Diethelm6,Hann von Weyhern Claus5,Neis Felix6,Haedicke-Jarboui Juliane1,Martus Peter7,Brucker Sara6,Henes Melanie6,Sasieni Peter34

Affiliation:

1. Institute of Medical Virology and Epidemiology of Viral Diseases, University Hospital Tübingen, Tübingen, Germany

2. Frauenärzte am Staden, Saarbrücken, Germany

3. Centre for Cancer Prevention, Queen Mary University of London, London, United Kingdom

4. Cancer Prevention Group, School of Cancer & Pharmaceutical Sciences, Faculty of Life Sciences & Medicine, King’s College London, London, United Kingdom

5. Department of Pathology and Neuropathology, University Hospital Tübingen, Tübingen, Germany

6. Department of Gynaecology and Obstetrics, University Hospital Tübingen, Tübingen, Germany

7. Medical Faculty Tübingen, Institute for Clinical Epidemiology and Applied Biometry, Tübingen, Germany

Abstract

Longitudinal data on the E6/E7 mRNA-based Aptima human papillomavirus (AHPV) assay exceeding three years in comparison to the gold standard Digene Hybrid Capture 2 (HC2) test are not available. We previously reported the cross-sectional data of the German AHPV Screening Trial (GAST) in which 10,040 women were recruited and tested by liquid-based cytology, the HC2 assay, and the AHPV assay.

Funder

Cancer Research UK

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

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