Using blood tests to monitor head and neck cancer
Official title: The Role of Circulating Tumour DNA in Head and Neck Cancer
Run by University of Edinburgh · NCT05539638 · Data updated 2026-11-12
This study is testing if blood tests can help monitor treatment and detect early relapse in people with HPV-related throat cancer.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 250 (estimated) |
| Sponsor | University of Edinburgh Academic / other |
| Locations | 5 sites (Dundee, DD2 1SG and 4 other locations) |
| Status | Recruiting |
| Started | August 14, 2022 |
| Main results expected | August 31, 2027 |
| Study ends | August 31, 2027 |
| Registry record updated | March 17, 2026 |
| Trial ID | NCT05539638 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are patients diagnosed with oropharyngeal squamous cell carcinoma, regardless of their HPV status.
✕Probably not a fit
Patients under 18 years of age, those lacking capacity to consent, or those with non-squamous cell carcinoma will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study focuses on oropharyngeal squamous cell carcinoma (OPSCC), particularly cases associated with human papillomavirus (HPV). The research aims to develop blood-based tests that detect circulating tumor DNA, providing a minimally invasive method for monitoring treatment response and identifying early relapse. By analyzing these DNA fragments shed by tumors, the study seeks to enhance clinical decision-making and improve patient outcomes. The study is set against the backdrop of increasing OPSCC incidence in Scotland and aims to address the limitations of current diagnostic techniques.
Why it matters
Potential benefit: If successful, this approach could lead to more accurate and timely monitoring of OPSCC, improving treatment outcomes for patients.
How similar studies have gone: Other studies have shown promise in using circulating tumor DNA for cancer monitoring, suggesting this approach could be effective.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients with oropharyngeal squamous cell carcinoma * Both HPV positive and negative disease Exclusion Criteria: * Patients under 18 years of age * Those who lack capacity to consent * Patients with non-squamous cell carcinoma * Patients with squamous cell carcinoma out with the oropharynx
Where it's running
-
Monklands Hospital ENT
Airdrie, United Kingdom Recruiting -
Glasgow Royal Infirmary
Glasgow, United Kingdom Recruiting -
Ninewells Hospital
Dundee, Dd2 1sg, United Kingdom Not yet recruiting -
Summerfield House - NHS Grampian
Aberdeen, United Kingdom Not yet recruiting -
The Royal Infirmiry
Edinburgh, United Kingdom Not yet recruiting
Study contacts
- Principal investigator: Ashley Tay — NHS Lothian
- Study coordinator: Iain Nixon
- Email: Iain.Nixon@nhslothian.scot.nhs.uk
- Phone: 07968498525
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Cervical screening and care options for women living with HIV who test positive for high-risk HPV
This study tests different ways to screen and manage high-risk HPV in women with HIV to see what might work best for them.
-
Docetaxel and SX-682 in head and neck cancers and prostate cancer
This trial tests a new drug SX-682 together with docetaxel in adults whose head and neck cancers or prostate cancer have returned or spread.
-
Lowering nodal and primary tumor radiation dose in HPV-positive oropharyngeal cancer
This phase II study tests whether reducing radiation doses to regions without visible cancer, while keeping the main tumor dose the same, can treat HPV-positive OPSCC with fewer side effects.
-
Selective dose reduction of neck radiation in HPV-associated oropharyngeal cancer
This trial tests whether lowering radiation doses to certain neck lymph nodes or gross disease areas is safe and can reduce side effects for adults with HPV-related oropharyngeal cancer.
-
Comparing dual-energy CT and MRI for staging oral and oropharyngeal squamous cell carcinoma
This will test whether 40 keV dual-energy CT can replace a contrast-enhanced neck and facial MRI for staging adults with oral or oropharyngeal squamous cell carcinoma.
-
Transtheoretical Model education to improve HPV vaccine knowledge and readiness in first-year nursing students
This program will try a Transtheoretical Model-based education to see if it increases first-year nursing students' HPV knowledge and makes them more ready to get the HPV vaccine.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.