TY - JOUR
T1 - Circulating cell-free HPV DNA is a strong marker for disease severity in cervical cancer
AU - Bønløkke, Sara
AU - Steiniche, Torben
AU - Sorensen, Boe Sandahl
AU - Nyvang, Gitte-Bettina
AU - Lindegaard, Jacob Christian
AU - Blaakaer, Jan
AU - Bertelsen, Jesper
AU - Fuglsang, Katrine
AU - Strube, Mikael Lenz
AU - Lenz, Suzan
AU - Stougaard, Magnus
PY - 2024/5
Y1 - 2024/5
N2 - 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.
AB - 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.
KW - HPV
KW - HPV integration
KW - Sedlis criteria
KW - cervical cancer
KW - circulating HPV DNA
KW - next-generation sequencing
KW - Severity of Illness Index
KW - Papillomavirus Infections/virology
KW - DNA, Viral/blood
KW - Biomarkers, Tumor/blood
KW - Humans
KW - Middle Aged
KW - Cell-Free Nucleic Acids/blood
KW - Uterine Cervical Neoplasms/virology
KW - Human papillomavirus 16/genetics
KW - Adult
KW - Female
KW - Aged
U2 - 10.1002/1878-0261.13538
DO - 10.1002/1878-0261.13538
M3 - Journal article
C2 - 37853962
SN - 1574-7891
VL - 18
SP - 1231
EP - 1244
JO - Molecular Oncology
JF - Molecular Oncology
IS - 5
ER -