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Study identifier: NCT05645783 Synced from ClinicalTrials.gov · August 08, 2026
● Study status: RecruitingENHANCE

Liquid Biopsy for Early DiagNosis of Squamous Cell Carcinoma of the HeAd and NeCk rEgion

Condition: Head and Neck Squamous Cell Carcinoma  ·  Sponsor: Royal Marsden NHS Foundation Trust

PhaseN/A
Planned participants170
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNoCheck eligibility criteria ↓
Where2 locations

Interested? Contact the study team ↓

Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.

About this study

The 5-year survival for Head and Neck squamous cell carcinoma (HNSCC) across all TNM stage groups is approximately 50%. Patients who are present with stage I \& II disease have significantly better survival. When a patient presents to their general practitioner (GP) with symptoms suggestive of HNSCC, they may be referred for urgent specialist input through the suspected cancer referral (SCR) pathway, which include dedicated neck lump clinics. HNSCC is known to shed fragments of DNA, called circulating tumor DNA (ctDNA) into the bloodstream. The investigators have developed novel ultra-sensitive (\>90% sensitivity) next generation sequencing (NGS) assay for circulating HPV DNA in patients with non-metastatic locally advanced head and neck cancer. The use of ultra-sensitive NGS assay for detection of ctDNA using a simple blood test (liquid biopsy) holds a great promise for cancer screening and early diagnosis and can lead to better survival results and less disease burden. With a quicker turnaround (1-2 weeks), the liquid biopsy can help expedite the patient journey through the cancer pathways reducing the incidence of cancer target breaches. In order to design studies to test this hypothesis the investigators require preliminary data quantifying sensitivity and specificity of the assay in this setting.

This description comes directly from the study's public registry record.

Talk to the study team

Shreerang Bhide  ·  02073528171  ·  Shreerang.Bhide@rmh.nhs.uk

Sarah Burton  ·  02073528171  ·  enhance@rmh.nhs.uk

There is no obligation to join — the study team can answer your questions about taking part.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

Inclusion Criteria: * Patients referred for an Ultrasound guided fine needle aspiration (USFNA) in the neck lump clinic Exclusion Criteria: * Patient found to have a lump in the thyroid gland at the time of USFNA * Unable to give informed consent for biological sample collection * Unable to safely participate in clinic sample collection

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (2)

Kingston Hospital Foundation TrustKingston upon Thames, United KingdomRecruiting
Northwick Park HospitalLondon, United KingdomNot Yet Recruiting

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Kingston upon ThamesLondon

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