% IMPORTANT: The following is UTF-8 encoded. This means that in the presence % of non-ASCII characters, it will not work with BibTeX 0.99 or older. % Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or % “biber”. @ARTICLE{Mittelstadt:274472, author = {S. Mittelstadt and O. Kelemen and J. Admard and A. Gschwind and A. Koch and S. Wörz and E. Oberlechner and T. Engler and I. Bonzheim and A. Staebler and N. Weidner and F. Stubenrauch and T. Iftner and O. Riess and C. Schroeder$^*$ and S. Kommoss and S. Ossowski$^*$}, title = {{D}etection of circulating cell-free {HPV} {DNA} of 13 {HPV} types for patients with cervical cancer as potential biomarker to monitor therapy response and to detect relapse.}, journal = {British journal of cancer}, volume = {128}, number = {11}, issn = {0007-0920}, address = {Edinburgh}, publisher = {Nature Publ. Group}, reportid = {DKFZ-2023-00617}, pages = {2097-2103}, year = {2023}, note = {2023 Jun;128(11):2097-2103}, abstract = {HPV-related cervical cancer (CC) is the fourth most frequent cancer in women worldwide. Cell-free tumour DNA is a potent biomarker to detect treatment response, residual disease, and relapse. We investigated the potential use of cell-free circulating HPV-DNA (cfHPV-DNA) in plasma of patients with CC.cfHPV-DNA levels were measured using a highly sensitive next-generation sequencing-based approach targeting a panel of 13 high-risk HPV types.Sequencing was performed in 69 blood samples collected from 35 patients, of which 26 were treatment-naive when the first liquid biopsy sample was retrieved. cfHPV-DNA was successfully detected in 22/26 $(85\%)$ cases. A significant correlation between tumour burden and cfHPV-DNA levels was observed: cfHPV-DNA was detectable in all treatment-naive patients with advanced-stage disease (17/17, FIGO IB3-IVB) and in 5/9 patients with early-stage disease (FIGO IA-IB2). Sequential samples revealed a decrease of cfHPV-DNA levels in 7 patients corresponding treatment response and an increase in a patient with relapse.In this proof-of-concept study we demonstrated the potential of cfHPV-DNA as a biomarker for therapy monitoring in patients with primary and recurrent CC. Our findings facilitate the development of a sensitive and precise, non-invasive, inexpensive, and easily accessible tool in CC diagnosis, therapy monitoring and follow-up.}, cin = {TU01}, ddc = {610}, cid = {I:(DE-He78)TU01-20160331}, pnm = {899 - ohne Topic (POF4-899)}, pid = {G:(DE-HGF)POF4-899}, typ = {PUB:(DE-HGF)16}, pubmed = {pmid:36973448}, doi = {10.1038/s41416-023-02233-x}, url = {https://inrepo02.dkfz.de/record/274472}, }