Journal Article DKFZ-2026-01427

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Detection of recurrence of HPV-driven oropharyngeal cancer by HPV cell-free DNA.

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2026
Springer Nature [London]

Scientific reports 16(1), 18349 () [10.1038/s41598-026-56914-7]
 GO

Abstract: The incidence of oropharyngeal cancer (OPC) driven by human papillomavirus (HPV) is increasing in high-income countries. Recurrent tumors remain a major cause of HPV-OPC mortality, yet reliable biomarkers for post-treatment monitoring are lacking. This study evaluated HPV cell-free DNA (cfDNA) from blood plasma as a monitoring biomarker for the detection of HPV-OPC recurrence. Blood plasma from 59 OPC patients was collected at diagnosis and during follow-up. HPV cfDNA was quantified using a multiplex digital PCR assay targeting HPV16 and seven other high-risk types. Tumor HPV status was confirmed by p16INK4A immunohistochemistry, HPV DNA PCR, and E6 serology. At diagnosis, HPV cfDNA was detected with 95% sensitivity (36/38; 95% CI 82-99%) and 95% specificity (19/20; 95% CI 75-100%). For 24 HPV-OPC patients, follow-up samples were available (median follow-up 1.5 years), with four patients experiencing recurrence or persistence of HPV-OPC. In two patients, HPV cfDNA detection after initial clearance preceded clinical recurrence by 3 and 8 months, respectively. The third patient experienced recurrence 7 months after collection of the last blood sample, which was HPV cfDNA-negative. The fourth patient had persistent disease without HPV cfDNA detection. HPV cfDNA positivity after therapy had a positive predictive value of 75% for HPV-OPC recurrence within one year on a per-test basis. HPV cfDNA has been shown to have great potential as a minimally invasive monitoring biomarker for HPV-OPC surveillance. Monitoring HPV cfDNA levels may identify patients at risk of recurrence early, thereby potentially facilitating timely intervention. Studies with more participants are needed to establish a solid evidence base for surveillance protocols that incorporate HPV cfDNA.

Keyword(s): Humans (MeSH) ; Oropharyngeal Neoplasms: virology (MeSH) ; Oropharyngeal Neoplasms: diagnosis (MeSH) ; Oropharyngeal Neoplasms: blood (MeSH) ; Female (MeSH) ; Cell-Free Nucleic Acids: blood (MeSH) ; Cell-Free Nucleic Acids: genetics (MeSH) ; Neoplasm Recurrence, Local: virology (MeSH) ; Neoplasm Recurrence, Local: diagnosis (MeSH) ; Neoplasm Recurrence, Local: blood (MeSH) ; DNA, Viral: blood (MeSH) ; DNA, Viral: genetics (MeSH) ; Papillomavirus Infections: virology (MeSH) ; Papillomavirus Infections: complications (MeSH) ; Papillomavirus Infections: blood (MeSH) ; Middle Aged (MeSH) ; Male (MeSH) ; Aged (MeSH) ; Human Papillomavirus Viruses: genetics (MeSH) ; Biomarkers, Tumor: blood (MeSH) ; Papillomaviridae: genetics (MeSH) ; Adult (MeSH) ; Cell-Free Nucleic Acids ; DNA, Viral ; Biomarkers, Tumor

Classification:

Note: #EA:C230#LA:C230#

Contributing Institute(s):
  1. Infektionen und Krebsepidemiologie (C230)
Research Program(s):
  1. 313 - Krebsrisikofaktoren und Prävention (POF4-313) (POF4-313)

Appears in the scientific report 2026
Database coverage:
Medline ; DOAJ ; Article Processing Charges ; BIOSIS Previews ; Biological Abstracts ; Clarivate Analytics Master Journal List ; Current Contents - Physical, Chemical and Earth Sciences ; DOAJ Seal ; Ebsco Academic Search ; Essential Science Indicators ; Fees ; IF < 5 ; JCR ; PubMed Central ; SCOPUS ; Science Citation Index Expanded ; Web of Science Core Collection ; Zoological Record
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 Record created 2026-06-15, last modified 2026-06-16



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