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Oesophageal CancerVALUENCT06440174

Understanding the Variation of Modern Endoscopic Ultrasound Use in Patients With Oesophageal Cancer (VALUE)

An observational study of Oesophageal Cancer, run by University Hospital Southampton NHS Foundation Trust at 14 sites in United Kingdom.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record

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Trial summary

This is an observational trial that will look at patients undergoing endoscopic ultrasound (EUS) in patients with oesophageal cancer and to determine the proportion of cases in which EUS changes disease management in these patients. Read more about this study

Who is it for?
Ages 16 years and older
Conditions the study is for
Oesophageal Cancer
What is being tested?
endoscopic ultrasound
Type of treatment
Surgery or procedure
How many people
160 participants
Where
14 sitesUnited Kingdom
Study dates
27 Jun 2024to 31 Dec 2026
How long will I take part?
6 Months
Phase
Observational

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 16 years and older
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Study population: Patients will be recruited through MDTs at participating secondary care centres in the UK. Those deemed suitable will be approached by their care team to take part.

Who may be able to join

  • Patients aged 16 or above with first diagnosis of biopsy-confirmed oesophageal cancer.
  • Referred for EUS examination as part of standard of care investigations.
  • Tumour location in the oesophagus, or gastro-oesophageal junction (Siewert types I-III)
  • MDT decision that patient is potentially curable with radical treatment (e.g., endoscopic treatment, surgery +/- neoadjuvant therapy, or definitive chemoradiotherapy)
  • Prior staging with CT and PET-CT
  • Eastern Cooperative Oncology Group (ECOG) performance status 0-2
  • Clinical staging of T1-T4, N0-N3, M0 disease
  • Adenocarcinoma or squamous cell carcinoma (SCC) histopathological cell type

Who cannot join

  • Recurrent or residual disease
  • Distant metastatic disease detected before EUS.
  • Previous oesophagectomy or oesophageal radiotherapy
  • Unable to undergo EUS examination.
  • Concurrent malignancy e.g., second primary tumour
  • Other histopathological cell type

Trial locations and contacts

14 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Ben Lindfield contact

023 8120 5154

value@soton.ac.uk

14 sites in 1 country

United Kingdom14 sites, 13 recruiting
  • Cwm Taf UHB

    Abercynon

    Lauren Geen, lauren.geen@wales.nhs.uk

    Recruiting
  • Royal Bournemouth Hospital

    Bournemouth

    Terminated
  • Cambridge University NHS Foundation Trust

    Cambridge

    Sophie Samra, sophie.samra@nhs.net

    Massimiliano di Pietro

    Recruiting
  • Cardiff and Vale UHB

    Cardiff

    Karen Arndell, karen.arndell2@wales.nhs.uk

    Recruiting
  • Velindre University NHS Trust

    Cardiff

    Emma John, emma.john3@wales.nhs.uk

    Kieran Foley

    Recruiting
  • Glasgow Royal Infirmary

    Glasgow

    Lauren Walker, Lauren.Walker5@nhs.scot

    Eliana Saffouri

    Recruiting
  • Castle Hill Hospital

    Hull

    Debbie Callaghan, debbie.callaghan3@nhs.net

    Rajarshi Roy

    Recruiting
  • Guy's and St Thomas' NHS Foundation Trust

    London

    Leeying Giet, l.giet@nhs.net

    Recruiting
  • Imperial College Healthcare NHS Trust

    London

    Quoc Nguyen, quoc.nguyen@nhs.net

    Christopher Peters

    Recruiting
  • Queen's Medical Centre, Nottingham

    Nottingham

    Emma Chamberlain, emma.chamberlain16@nhs.net

    Recruiting
  • Salford Royal Hospital

    Salford

    Sadaf Naveed, sadaf.naveed@nca.nhs.uk

    Recruiting
  • University Hospital Southampton

    Southampton

    Donna Graham, donna.graham@uhs.nhs.uk

    Nadeem Tehami

    Recruiting
  • Singleton Hospital, Swansea

    Swansea

    Esther Reeves, esther.reeves@wales.nhs.uk

    Recruiting
  • Royal Cornwall Hospital

    Truro

    Sally Thomas, sally.thomas23@nhs.net

    Dushyant Shetty

    Recruiting

Other trials in United Kingdom

About this study

Official title: Understanding the Variation of Modern Endoscopic Ultrasound Use in Patients With Oesophageal Cancer (VALUE): a Multi-methods Study

This is an observational trial that will look at patients undergoing endoscopic ultrasound (EUS) in patients with oesophageal cancer and to determine the proportion of cases in which EUS changes disease management in these patients.

Read the detailed description

Over 9,000 patients are diagnosed with oesophageal cancer in the United Kingdom (UK) annually. The prognosis of these patients is poor, with an overall 5-year survival rate of 15%.

Most patients (60%) present with advanced disease and palliation is the only treatment option. Accordingly, oesophageal cancer has considerable unmet research need.

The VALUE trial is a prospective observational study investigating EUS in the modern era of oesophageal cancer staging. A quantitative study component will examine how often and why EUS changes treatment decisions after initial staging with CT and PET-CT. A qualitative study component will explore both clinician and patient attitudes and opinions towards the utility of EUS in the staging pathway.

EUS is an invasive procedure combining upper gastrointestinal endoscopy with ultrasonography. An ultrasound probe located at the end of the endoscope allows direct visualisation of the oesophageal wall layers and adjacent tissues providing local assessment of the depth of tumour invasion and lymph nodes. This assessment informs local tumour (T-) and node (N-) staging which are important prognostic indicators of survival. Patients undergoing EUS require sedation and there are risks of complication. EUS is a specialist investigation requiring many years of dedicated training to perform competently.

VALUE aims to recruit patients with oesophageal cancer who are deemed to have potentially curable disease and who are fit for, and wish to have, radical treatment, and who receive EUS as part of their standard of care staging pathway. Patients with a range of disease status (T1-T4; N0-N3) will be considered for recruitment to allow diverse consideration of the reasons whether EUS impacts treatment decisions in current clinical practice. VALUE will also recruit clinicians who regularly care for oesophageal cancer patients in a multi-disciplinary setting to gather their opinions regarding the use of EUS in this patient population.

A systematic review, updating a prior review, found that current evidence concerning the impact of EUS on the management and outcome of oesophageal cancer patients in modern staging with PET-CT was of limited quality. In total, 18 studies with 11,836 patients were included. Overall, 2,805 patients (23.7%) underwent EUS compared to 9,031 (76.3%) without. However, only 19.7% of all patients also had PET-CT for staging. Reported change of management by EUS varied widely from 0% to 56%.

EUS use in oesophageal cancer patients across the NHS is also reported to vary widely. Considerable variation in EUS practice was found in a survey of oesophageal cancer multi-disciplinary team (MDT) leads across the UK. Eighty-seven of 97 UK NHS trusts responded. 29% recommended EUS for all potentially curable patients whereas 46% requested EUS after PET-CT on a case-by-case basis. 20% reported both a lack of utility and concerns about treatment delay. Overall, 63% and 43% routinely use EUS for radiotherapy and surgical planning, respectively. Further, data from the National Oesophago-Gastric Cancer Audit (NOGCA) all describe the reported decline in EUS use from 62% of all patients in 2013, to 39% in 2019, and 18.6% to 2021. In 2020/21, EUS was used in 23.6% of patients who had a curative treatment plan.

The Cancer of Oesophagus or Gastricus-New Assessment of Technology of Endosonography (COGNATE) trial randomised patients between EUS with CT, and CT alone. EUS led to improved quality-adjusted survival. However, since COGNATE, oesophageal cancer staging has been transformed by PET-CT, a cross-sectional nuclear imaging test usually performed prior to EUS. PET-CT has greater sensitivity for distant metastases than CT, and therefore identifies more patients unsuitable for radical treatment, meaning that local staging with EUS becomes less critical in these patients.

This conclusion is supported by data from a large retrospective cohort study by Findlay et al which included 953 patients, of which 798 had EUS, and 918 had PET-CT. The authors found that patient management was changed by EUS in 11% of cases, but when probability thresholds were calculated, the utility of EUS in the majority of patients (71.8% staged T2-T4a) was minimal (0.4%), concluding that the risk of EUS exceeded its benefit. However, these data have not been validated outside of this single-centre study but does question the value of EUS in the modern staging pathway.

In summary, the use of PET-CT for oesophageal cancer staging is increasing, and use of EUS declining, which supports the modern tendency of clinicians to favour non-invasive cross-sectional imaging. However, evidence supporting the basis for this recent change in practice is limited.

There will also be a qualitative part of the trial where a qualitative researcher will interview 30 patients who consent to this in the patient information sheet and 30 clinicians who can carry out EUS, and ask both for their opinions and thoughts on the procedure.

Being tested
endoscopic ultrasound
Medical subject headings
Esophageal Neoplasms

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • endoscopic ultrasoundProcedure or surgery

    EUS is an invasive procedure combining upper gastrointestinal endoscopy with ultrasonography. An ultrasound probe located at the end of the endoscope allows direct visualisation of the oesophageal wall layers and adjacent tissues providing local assessment of the depth of tumour invasion and lymph nodes. This assessment informs local tumour (T-) and node (N-) staging which are important prognostic indicators of survival. Patients undergoing EUS require sedation and there are risks of complication. EUS is a specialist investigation requiring many years of dedicated training to perform competently.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Number of patients who change treatment management

    to determine if using EUS after CT-PET changes management.

    Measured: this decision will be made at baseline.

Secondary outcomes (3)
  1. Number of clinicians and patients who will share their opinions on EUS by a one to one interview with a qualitative researcher.

    The voluntary one to one interview which patients will consent to on the informed consent form, will be used to identify factors that patients consider when deciding whether EUS should be used. This will take place on Microsoft Teams, hosted by the SCTU qualitative researcher. The interview will be recorded and accurately transcribed and once this has taken place, the interview will be deleted. The anonymised transcript can be stored for up to 10 years with the University of Southampton research data management policy.

    Measured: This will take place up to 6 weeks following the EUS at one to one interviews.

  2. Number of patients who changed their treatment management following EUS.

    to determine the reasons why EUS changed management.

    Measured: this decision will be made at baseline.

  3. Number of patients who decided on their treatment.

    to determine the time from diagnosis to treatment decision before and after EUS.

    Measured: this decision will be made at baseline.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted3 Jun 2024
  2. Study start27 Jun 2024
  3. Primary completion30 Jun 2026 (estimated)
  4. Study completion31 Dec 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
160 participants (estimated)
Target duration
6 Months
IDs, dates and publications
ClinicalTrials.gov ID
NCT06440174
Sponsor's protocol ID
CAN1794
Acronym
VALUE
Status last verified
Apr 2026
First submitted
8 May 2024
Last updated
30 Apr 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Foley KG, Boxall C, Franklin J, Cook A, Underwood T, Griffiths G, Cozens K, Bradbury K, Fay M, Chuter D, Longman KA, Lindfield B, Hurt C. Understanding the variation of modern endoscopic ultrasound use in patients with oesophageal cancer (VALUE): protocol for a multi-methods study. BJR Open. 2025 May 21;7(1):tzaf012. doi: 10.1093/bjro/tzaf012. eCollection 2025 Jan.

    PubMed 40486070

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