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Circulating cell-free HPV DNA is a strong marker for disease severity in cervical cancer.
Bønløkke, Sara; Steiniche, Torben; Sorensen, Boe Sandahl; Nyvang, Gitte-Bettina; Lindegaard, Jacob Christian; Blaakaer, Jan; Bertelsen, Jesper; Fuglsang, Katrine; Strube, Mikael Lenz; Lenz, Suzan; Stougaard, Magnus.
Afiliación
  • Bønløkke S; Department of Clinical Medicine, Aarhus University, Denmark.
  • Steiniche T; Department of Pathology, Aarhus University Hospital, Denmark.
  • Sorensen BS; Department of Clinical Medicine, Aarhus University, Denmark.
  • Nyvang GB; Department of Pathology, Aarhus University Hospital, Denmark.
  • Lindegaard JC; Department of Clinical Medicine, Aarhus University, Denmark.
  • Blaakaer J; Department of Clinical Biochemistry, Aarhus University Hospital, Denmark.
  • Bertelsen J; Department of Oncology, Odense University Hospital, Denmark.
  • Fuglsang K; Department of Oncology, Aarhus University Hospital, Denmark.
  • Strube ML; Department of Obstetrics and Gynecology, Odense University Hospital, Denmark.
  • Lenz S; Department of Clinical Research, University of Southern Denmark, Odense M, Denmark.
  • Stougaard M; Department of Pathology, Aarhus University Hospital, Denmark.
Mol Oncol ; 2023 Oct 19.
Article en En | MEDLINE | ID: mdl-37853962
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.
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Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Mol Oncol Asunto de la revista: BIOLOGIA MOLECULAR / NEOPLASIAS Año: 2023 Tipo del documento: Article País de afiliación: Dinamarca

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Mol Oncol Asunto de la revista: BIOLOGIA MOLECULAR / NEOPLASIAS Año: 2023 Tipo del documento: Article País de afiliación: Dinamarca