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NCT07407205Active, not recruiting

Tumor Mutational Burden, Liquid Biopsy, Angiogenic Factors and DCE-MRI Perfusion in HPV-Negative Oropharyngeal Cancer

Tumor Mutational Burden, Liquid Biopsy, Angiogenic Factors and Magnetic Resonance Perfusion in Predicting Response to Chemoradiotherapy in HPV-Negative Oropharyngeal Squamous Cell Carcinoma and Disease Course After Treatment

Source: ClinicalTrials.gov · Last updated 17 Feb 2026

Brief summary (registry, in English)

This prospective interventional study evaluates the predictive value of tumor mutational burden, liquid biopsy biomarkers (including circulating tumor DNA), angiogenic factors, and dynamic contrast-enhanced magnetic resonance (MR) perfusion imaging in patients with HPV-negative oropharyngeal squamous cell carcinoma treated with concurrent chemoradiotherapy. The aim is to improve prediction of treatment response and disease course after treatment, support decision-making regarding optimal therapy, and potentially reduce the number of imaging examinations required during follow-up.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
30 (estimated)
First submitted
6 Feb 2026
Start date
10 Jun 2019
Primary completion date
31 Dec 2025
Lead sponsor
Institute of Oncology Ljubljana
NCT number
NCT07407205

What you commit to

  • Study type: Interventional
  • Planned participants: 30
  • From 10 Jun 2019 to the primary completion date, 31 Dec 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • HPV-positive oropharyngeal carcinoma
  • Contraindications for MRI
  • Severe comorbidities preventing chemoradiotherapy
  • Pregnancy or breastfeeding
  • Inability to comply with study procedures

Who the study is looking for

  • Age ≥ 18 years
  • Histologically confirmed HPV-negative oropharyngeal squamous cell carcinoma
  • Planned treatment with concurrent chemoradiotherapy
  • Ability to undergo MRI examination
  • Signed informed consent

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Institute of Oncology Ljubljana
Coordinator of this site? Confirm its status
LjubljanaSloveniaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.