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UNKNOWNN/A

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

Sponsor: Royal Marsden NHS Foundation Trust

NCT ID: NCT05645783

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Health checks and monitoring — no treatment given
Type of study
Observational (no treatment given)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
Not specified by the sponsor
How long the study runs
Study runs about 22 months (dates as stated)
About the drug or intervention
Not specified by the sponsor
Patient visit burden
Not specified by the sponsor
Type of study
Observing health over time
Ages
18 Years and over
Who
All
Number of participants
170
Started
2023-02-01
Last checked
2024-08

Plain English Summary

What is this study?

  • • Testing a new treatment for head and neck squamous cell carcinoma
  • • Clinical study - 170 participants
  • • The 5-year survival for Head and Neck squamous cell carcinoma (HNSCC) across all TNM stage groups is approximately 50%

Who can take part?

  • • Ages 18 Years and over
  • • Diagnosed with head and neck squamous cell carcinoma

Where?

  • • Kingston upon Thames - Kingston Hospital Foundation Trust
  • • London - Northwick Park Hospital

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

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.

More detail

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. Majority of the patients diagnosed via the SCR pathway present with Stage III \&IV disease, which has a direct impact on outcomes. HNSCC is classified as an uncommon cancer and as such diagnosis and treatment is undertaken in specialist tertiary referral centres. The care of patients initially diagnosed with HNSCC in smaller secondary care hospitals is transferred to these specialist tertiary referral centres via the Inter Trust Transfer (ITT). ITT can introduce delays in treatment pathways resulting in a failure to achieve cancer treatment targets. Southwest London HNSCC diagnostic pathway review which was undertaken in February 2021 demonstrated that 40% of ITTs received were greater than 38 days after referral and that 68% of the 62 day target breaches were in patients with ITT. 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 investigator's current work involves ctDNA detection to cover the spectrum of genetic alterations in HNC using a single sequencing workflow to detect copy number aberrations (CNAs), HPV DNA (to cover 99.9% of HNC related HPV) and somatic mutations. 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. This has been proven in proof of principle studies in nasopharyngeal cancer (Chan N Engl J Med 2017; 377:513-522). Furthermore, this test can be administered in smaller secondary care hospitals in parallel to the ITT. 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.

Head and Neck Squamous Cell Carcinoma

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What we know so far

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Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 18 Years and over
  • Who can join: All genders

What the study is looking for

  • ✓Patients referred for an Ultrasound guided fine needle aspiration (USFNA) in the neck lump clinic

Who cannot take part

  • ✗Patient found to have a lump in the thyroid gland at the time of USFNA
  • ✗Unable to give agreement to take part for biological sample collection
  • ✗Unable to safely participate in clinic sample collection
See the full criteria
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

Where Is This Study? (2 UK sites)

Kingston Hospital Foundation Trust

Kingston upon Thames KT27QB, United Kingdom

Recruiting
Site contact (verified)
Enyi OfoPrincipal Investigator

Northwick Park Hospital

London HA13UJ, United Kingdom

NOT_YET_RECRUITING
Site contact (verified)
Liu Zi-WeiPrincipal Investigator

How to Get in Touch

Shreerang Bhide

Sponsor contact

CONTACT

02073528171 Shreerang.Bhide@rmh.nhs.uk

Sarah Burton

Sponsor contact

CONTACT

02073528171 enhance@rmh.nhs.uk
Data sourced from ClinicalTrials.gov · Last verified: 2024-08