Abstract 880P
Background
Globally the incidences of oropharyngeal squamous cell carcinoma (OPSCC), especially those associated with high-risk human papillomavirus are rising. Although patients with HPV-positive OPSCC present with better survival, up to 25% develop recurrent disease. Biomarkers to monitor therapy response, minimal residual disease and tumor burden during follow-up are urgently needed. The detection of cell-free (cf)HPV-DNA in blood plasma offers the opportunity for minimally invasive disease monitoring and early recurrence detection.
Methods
We examined 34 patients with HPV-related OPSCC and 21 controls (healthy donors and HPV-negative OPSCC patients) to investigate cfHPV16-DNA status prior to and during therapy as well as throughout follow-up. qPCR and ddPCR were applied to quantify the concentration of cfHPV16-DNA in plasma, using the viral gene E6 as a target.
Results
No cfHPV16-DNA or <10 copies per ml plasma were detected in healthy donors or HPV-negative OPSCC patients. Plasma samples from patients with HPV-positive OPSCC collected prior to treatment. At the cut-off of 10 copies/ml plasma, ddPCR showed 79% sensitivity, 80% specificity, 70% NPV, and 90% PPV, whereas qPCR showed 73% sensitivity, 80% specificity, 60% NPV, 90% PPV. Patients without clinical evidence of recurrence had significantly lower cfHPV16-DNA concentrations after therapy, whereas increase of copy number was correlated to recurrent disease.
Conclusions
Our results demonstrate that ddPCR is a more sensitive method compared to qPCR for detection of cfHPV16-DNA in plasma of patients with HPV16-positive OPSCC. cfHPV16-DNA correlated with tumor burden and therefore presents a promising diagnostic tool. Nevertheless, prospective studies with expanded patient cohorts are necessary to investigate the kinetics of cfHPV16-DNA in relation to therapy response and the development of recurrent and metastatic disease.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
Dr. Nora Würdemann.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
878P - INHBA is overexpressed in HPV-negative oropharyngeal squamous cell carcinoma and contributes to an aggressive phenotype
Presenter: Simon Laban
Session: Poster session 12
881P - SOTO study: Prospective study to correlate the treatment sensitivity of patient-derived organoids (PDOs) with treatment outcomes in head and neck cancer patients
Presenter: Ifigenia Vasiliadou
Session: Poster session 12
882P - Claudin-1 (CLDN1) expression in head and neck squamous cell carcinoma (HNSCC) patients
Presenter: Stefano Cavalieri
Session: Poster session 12
884P - Prognostic value and immune characteristics of LGALS1 in head and neck squamous cell carcinoma
Presenter: Yanfei Min
Session: Poster session 12
885P - Clinical significance of folate receptor-positive circulating tumor cells detected by ligand-targeted polymerase chain reaction in nasopharyngeal carcinoma
Presenter: Dingyi Wang
Session: Poster session 12
887P - Antitumor activity of the radioenhancer NBTXR3 on injected lesions to estimate overall survival: Exploratory analyses from a phase I in cisplatin-ineligible locally advanced HNSCC patients
Presenter: Christophe Le Tourneau
Session: Poster session 12
888P - Phase I study of olaparib combined with loco-regional radiotherapy in patients with head and neck squamous cell carcinoma
Presenter: Marcel Verheij
Session: Poster session 12
889P - CT-based radiomics models to predict progression in locally advanced head and neck cancer treated with definitive chemoradiation
Presenter: Gema Bruixola
Session: Poster session 12