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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT06453993
Other study ID # CRP19015
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date December 1, 2019
Est. completion date June 28, 2024

Study information

Verified date June 2024
Source Benaroya Research Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to investigate whether exhaled breath can be used to detect and monitor esophageal cancer.


Description:

Esophageal cancer ("EG cancer") affects over half a millions people worldwide every year. Early esophageal cancer typically has non-specific symptoms that are often mistaken for benign (non-cancer) conditions. As a result, patients are often referred for further investigations only when they have more prominent symptoms that are typically associated with advanced incurable disease. As a consequence, 7 out of 10 new cases of EG cancer diagnosed are considered to be at an advanced stage, with less than 1 in 3 patients eligible for potentially curative therapy. Better ways of diagnosing esophageal cancer earlier are therefore needed. An ideal test for esophageal cancer would be non-invasive, simple to administer in the community, and cost effective. The investigators' approach to this clinical challenge is to establish a non-invasive test for the detection of esophageal cancer that is based upon the unique signature of small molecules within exhaled breath. In this study that is being conducted in collaboration with researchers in the United Kingdom (UK), the investigators would like to measure the levels of these small molecules within the breath of patients with esophageal cancer at different times during their treatment: (i) at diagnosis; (ii) after chemoradiotherapy, and; (iii) after surgery. By studying how the small molecules contained within the breath change as a result of esophageal cancer and its treatment, the investigators hope to learn new information that can help develop a new test for this disease. The investigators will also measure the small molecules within saliva and urine samples collected at the same time as breath in order to study if there are any important differences between these three samples. The investigators will also attempt to measure different bacteria


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 46
Est. completion date June 28, 2024
Est. primary completion date December 28, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria: - Aged 18-90 years - Newly-diagnosed, treatment naïve patients with esophageal and/or gastroesophageal junctional cancer - Planning to undergo curative treatment, including neoadjuvant chemoradiotherapy and surgical resection Exclusion Criteria: - Pregnant females - Without malignant esophageal disease - Malignancy at a secondary site other than the esophagus - Undergoing palliative treatment for esophageal cancer - Not receiving neoadjuvant chemoradiotherapy and surgical resection for esophageal cancer - Inability or unwillingness to provide written informed consent

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Exhaled VOC breath test
To determine longitudinal variation in exhaled VOC concentrations during intended curative therapy for EC cancer.

Locations

Country Name City State
United Kingdom Imperial College London London
United States Virginia Mason Medical Center Seattle Washington

Sponsors (2)

Lead Sponsor Collaborator
Benaroya Research Institute Imperial College London

Countries where clinical trial is conducted

United States,  United Kingdom, 

References & Publications (2)

Antonowicz S, Bodai Z, Wiggins T, Markar SR, Boshier PR, Goh YM, Adam ME, Lu H, Kudo H, Rosini F, Goldin R, Moralli D, Green CM, Peters CJ, Habib N, Gabra H, Fitzgerald RC, Takats Z, Hanna GB. Endogenous aldehyde accumulation generates genotoxicity and ex — View Citation

Kamal F, Kumar S, Edwards MR, Veselkov K, Belluomo I, Kebadze T, Romano A, Trujillo-Torralbo MB, Shahridan Faiez T, Walton R, Ritchie AI, Wiseman DJ, Laponogov I, Donaldson G, Wedzicha JA, Johnston SL, Singanayagam A, Hanna GB. Virus-induced Volatile Orga — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Exhaled breath and urinary VOC concentrations as biomarkers of esophageal cancer The composition and concentration of volitile organic compounds (VOC) in exhaled breath and urinary samples will be assessed to establish a VOC signature of esophogeal cancer Before commencing treatment for esophageal cancer
Secondary Changes in VOC concentrations that occur in response to therapeutic intervention VOC concentrations in exhaled breath and urinary samples will be assessed longitudinally to assess how VOC concentrations change in response to therapeutic intervention (i) Before commencing treatment for esophageal cancer, (ii) About 4 - 6 weeks after neoadjuvant therapy, (iii) About 3 - 5 days after surgical resection (but before hospital discharge), (iv) At routine follow up (6 - 12 months after surgery)
Secondary Linkage of longitudinal VOC data to predominant upper gastrointestinal bacterial species Bacterial RNA will be extracted from saliva samples to identify bacterial composition. Bacterial composition will then be correlated with breath and urinary VOC levels (i) Before commencing treatment for esophageal cancer, (ii) About 4 - 6 weeks after neoadjuvant therapy, (iii) About 3 - 5 days after surgical resection (but before hospital discharge), (iv) At routine follow up (6 - 12 months after surgery)
Secondary Patient acceptability of breath test Study subjects will be asked to complete a short survey designed to assess their understanding and opinions regarding breath testing Before commencing treatment for esophogeal cancer
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