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The Diagnostic Value of Circulating Cell-Free HPV DNA in Plasma from Cervical Cancer Patients

Authors :
Sara Bønløkke
Magnus Stougaard
Boe Sandahl Sorensen
Berit Bargum Booth
Estrid Høgdall
Gitte-Bettina Nyvang
Jacob Christian Lindegaard
Jan Blaakær
Jesper Bertelsen
Katrine Fuglsang
Mikael Lenz Strube
Suzan Lenz
Torben Steiniche
Source :
Cells, Vol 11, Iss 14, p 2170 (2022)
Publication Year :
2022
Publisher :
MDPI AG, 2022.

Abstract

Circulating cell-free HPV DNA (ccfHPV DNA) may serve as a marker for cervical cancer. In this study, we used digital droplet PCR (ddPCR) to detect and quantify ccfHPV DNA in plasma from patients with HPV16- or HPV18-associated cervical cancer. Blood samples from 60 patients diagnosed with cervical cancer (FIGO IA1-IVA) at Aarhus or Odense University Hospital (June 2018 to March 2020) were collected prior to treatment, and patients were subdivided into an early stage (n = 30) and a late-stage subgroup (n = 30) according to disease stage. Furthermore, blood samples from eight women with HPV16- or 18-associated premalignant conditions (CIN3), and 15 healthy controls were collected. ddPCR was used to analyze plasma from all participants. ccfHPV DNA was detected in 19 late-stage patients (63.33%), 3 early stage patients (10.00%), and none of the CIN3 patients or controls. Quantitative evaluation showed significant correlations between ccfHPV DNA level and stage, tumor score, and tumor size. Thus, our results indicate that ccfHPV DNA may not be a useful marker for early detection of cervical cancer. However, for patients with advanced stage cervical cancer, ccfHPV DNA level represents a promising tool to establish tumor burden, making it useful for establishing treatment response and monitoring the disease.

Details

Language :
English
ISSN :
11142170 and 20734409
Volume :
11
Issue :
14
Database :
Directory of Open Access Journals
Journal :
Cells
Publication Type :
Academic Journal
Accession number :
edsdoj.06bef8557aa5496f8f8b269ac5a6d902
Document Type :
article
Full Text :
https://doi.org/10.3390/cells11142170