TY - JOUR
T1 - The Diagnostic Value of Circulating Cell-Free HPV DNA in Plasma from Cervical Cancer Patients
AU - Bønløkke, Sara
AU - Stougaard, Magnus
AU - Sorensen, Boe Sandahl
AU - Booth, Berit Bargum
AU - Høgdall, Estrid
AU - Nyvang, Gitte Bettina
AU - Lindegaard, Jacob Christian
AU - Blaakær, Jan
AU - Bertelsen, Jesper
AU - Fuglsang, Katrine
AU - Strube, Mikael Lenz
AU - Lenz, Suzan
AU - Steiniche, Torben
N1 - Funding Information:
This research was funded by IMK Almene Fond, grant number 30-206-365; Civilingeniør Frode V. Nyegaard og hustrus fond, grant number 12-06-2018; Fabrikant Einar Willumsens Mindelegat, grant number 6000073; Folketingsmand J. Christensen og hustrus K. Christensens Fond til støtte af forskning i kræft- og AIDS-sygdomme, grant number 21012021; Grosserer A.V. Lykfeldts og Hustrus legat, grant number 27022021; Harboefonden, grant number 19181; Holms Mindelegat, grant number 20006-1902; Inge og Jørgen Larsens mindelegat, grant number 105 37-05; Krista og Viggo Petersens Fond, grant number 6030/67; Søster og Verner Lipperts fond, grant number 13-12-2017; Vissingfonden, grant number 54622; and Aase og Ejnar Danielsens Fond, grant number 10-002130.
PY - 2022/7
Y1 - 2022/7
N2 - 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.
AB - 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.
KW - ccfHPV DNA
KW - cervical cancer
KW - circulating cell-free DNA
KW - circulating cell-free HPV DNA
KW - circulating tumor DNA
KW - ctDNA
KW - ddPCR
KW - digital droplet PCR
KW - HPV
KW - human papillomavirus
U2 - 10.3390/cells11142170
DO - 10.3390/cells11142170
M3 - Journal article
C2 - 35883612
AN - SCOPUS:85136248540
VL - 11
JO - Cells
JF - Cells
SN - 2073-4409
IS - 14
M1 - 2170
ER -