COlorectal BReath Analysis (COBRA2)
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Details and patient eligibility
About
Colorectal cancer (CRC) is the second most common cause of cancer death in the United Kingdom, with approximately 17,000 deaths per year. The five-year survival rate from CRC is only 10% when discovered at a late stage, but exceeds 90% if diagnosed early. Symptoms related to CRC can be non-specific, therefore the decision to refer for a colonoscopy can be challenging.
There is a clear need to improve earlier detection of CRC so that patients with CRC can be identified earlier and faster, enabling them to start treatment more quickly.
The study team is developing a non-invasive breath test that detects small molecules called volatile organic compounds (VOCs) that are specific to CRC. For patients with non-specific symptoms, this test would help GPs to identify those patients that may have underlying CRC, who would benefit from referral for specialised CRC tests.
Full description
The COBRA1 study initially assessed VOCs in CRC and identified a list of 14 VOC biomarkers for CRC and provided a detection model with an area under the receiver operating characteristic curve of 0.91, sensitivity of 83% and specificity of 88% in symptomatic patients.
COBRA2 aims to develop and validate the clinical prediction model (CPM) in the detection of CRC based on the breath test. An exploratory comparison between the breath test and faecal immunochemical test (FIT) will also be carried out to assess whether combining both tests improves diagnostic performance.
Methods: COBRA2 is be a prospective, multicentre validation study. The study team are recruiting the following patients:
The following groups of patients are being recruited:
i) Control group: symptomatic patients who are attending a planned colonoscopy referred under the suspected lower GI cancer pathway. Any patient who is found to have histologically-proven CRC on colonoscopy will be analysed as part of the CRC group.
ii) CRC group: patients who either have a confirmed diagnosis of colorectal adenocarcinoma according to a biopsy, or who are due to undergo surgical resection for suspected CRC (with histological confirmation to follow within three months).
Target recruitment is 720 patients (470 controls, 250 CRC), aiming for 576 patients (376 controls, 200 CRC) with reliable and complete data. Participants are required to maintain a clear fluid diet for a minimum of 4-6 hours prior to sampling and should not have received bowel preparation. Participants will be asked to provide breath samples by exhaling into single-use breath collection bags and breath will be transferred using a precision pump onto thermal desorption (TD) tubes. Breath samples will be analysed with gas chromatography-mass spectrometry in accordance with existing quality control processes.
Enrollment
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Inclusion and exclusion criteria
Inclusion Criteria:
- Patients aged ≥ 18 years referred from primary care with symptoms of suspected CRC.
- Patients with histologically confirmed colorectal adenocarcinoma (stages I-IV) who are treatment naïve (CRC group).
Exclusion Criteria - patients with any of the following will not be eligible for inclusion:
- Previous surgery altering the anatomy of the lower GI tract (e.g., hemicolectomy, anterior resection).
- Previous treatment (neoadjuvant chemotherapy or radiotherapy or immunotherapy) for CRC.
- Received bowel preparation for their colonoscopy procedure.
- History of any other cancer within three years.
- Unable or unwilling to provide informed written consent.
Trial design
720 participants in 2 patient groups
Trial contacts and locations
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Central trial contact
Mr Michael G Fadel, BSc MBBS MRCS
Data sourced from clinicaltrials.gov
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