Circulating cell‐free HPV DNA is a strong marker for disease severity in cervical cancer

Author:

Bønløkke Sara12ORCID,Steiniche Torben12,Sorensen Boe Sandahl13,Nyvang Gitte‐Bettina4,Lindegaard Jacob Christian5,Blaakær Jan67,Bertelsen Jesper2,Fuglsang Katrine18,Strube Mikael Lenz9,Lenz Suzan10,Stougaard Magnus12

Affiliation:

1. Department of Clinical Medicine Aarhus University Denmark

2. Department of Pathology Aarhus University Hospital Denmark

3. Department of Clinical Biochemistry Aarhus University Hospital Denmark

4. Department of Oncology Odense University Hospital Denmark

5. Department of Oncology Aarhus University Hospital Denmark

6. Department of Obstetrics and Gynecology Odense University Hospital Denmark

7. Department of Clinical Research University of Southern Denmark Odense M Denmark

8. Department of Obstetrics and Gynecology Aarhus University Hospital Denmark

9. DTU Bioengineering Technical University of Denmark Kongens Lyngby Denmark

10. Private Gynecological Clinic “Suzan Lenz Gynækolog” Copenhagen Denmark

Abstract

For cervical cancer (CC), circulating cell‐free HPV DNA (ccfHPV) may establish disease severity. Furthermore, HPV integration has been correlated to viral load and survival. In this study, pre‐treatment plasma from 139 CC cases (50 primary surgery patients, 22 primary surgery + adjuvant oncological therapy patients, and 67 primary oncological therapy patients) was collected (2018–2020). Furthermore, plasma from 25 cervical intraepithelial neoplasia grade 3 patients and 15 healthy women (negative controls) were collected. Two next‐generation sequencing (NGS) panels were used to establish ccfHPV presence and human papillomavirus type 16 (HPV16) integration status. ccfHPV was detected in four primary surgery (8.0%), eight primary surgery + adjuvant oncology (36.4%), and 54 primary oncology (80.6%) patients. For primary oncology patients with HPV16‐related cancer (n = 37), more ccfHPVneg than ccfHPVpos patients had HPV16 integration (P = 0.04), and in patients with HPV16 integration (n = 13), ccfHPVpos patients had higher disease stages than ccfHPVneg patients (P = 0.05). In summary, ccfHPV presence is related to disease severity and may add to the debated Sedlis criteria used for identifying patients for adjuvant oncological therapy. However, ccfHPV detection is influenced by HPV integration status and disease stage, and these factors need to be considered in ccfHPVneg patients.

Funder

Aase og Ejnar Danielsens Fond

Fabrikant Einar Willumsens Mindelegat

Harboefonden

Inge og Jørgen Larsens Mindelegat

Ingeniør K. A. Rohde og hustrus Legat

KV Fonden

Publisher

Wiley

Subject

Cancer Research,Genetics,Molecular Medicine,General Medicine,Oncology

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