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 ccfHPV than ccfHPV patients had HPV16 integration (P = 0.04), and in patients with HPV16 integration (n = 13), ccfHPV patients had higher disease stages than ccfHPV 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 ccfHPV patients.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11076984PMC
http://dx.doi.org/10.1002/1878-0261.13538DOI Listing

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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).

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Article Synopsis
  • More than 99% of cervical cancers and 40% of vulvar cancers are caused by a virus called HPV, especially types 16 and 18.
  • Scientists are testing a new way to detect tiny bits of HPV DNA in blood to help monitor cancer treatment.
  • They found that the amount of HPV DNA in the blood dropped a lot after treatment, indicating that this method could help doctors see if the treatment is working, especially for more advanced cancer cases.
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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 ( = 30) and a late-stage subgroup ( = 30) according to disease stage.

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