Screening for liver metastases in high-risk colorectal cancer patients using MRI
Screening for Synchronous Metastases in Colorectal Cancer With DW-MRI.
This study is testing if a special type of MRI can find liver cancer spread earlier in patients with high-risk colorectal cancer compared to regular CT scans.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 282 (estimated) |
| Ages | 16 Years and up |
| Sex | All |
| Sponsor | Imperial College London Academic / other |
| Locations | 13 sites (Macclesfield, Cheshire and 12 other locations) |
| Trial ID | NCT02246634 on ClinicalTrials.gov |
What this trial studies
This study aims to evaluate the effectiveness of Diffusion Weighted MRI (DW-MRI) in detecting synchronous liver metastases in patients with high-risk colorectal cancer, compared to standard CT imaging. Eligible participants will undergo DW-MRI scans every six months for three years following surgery, provided they have no prior evidence of liver metastases. The findings from these scans will be shared with local multidisciplinary teams (MDTs) to guide treatment decisions for any identified liver metastases. The goal is to improve early detection and management of metastatic disease.
Who should consider this trial
Good fit: Ideal candidates are patients aged 16 years or older with high-risk primary colorectal malignancies and no prior evidence of liver metastases.
Not a fit: Patients with previous colorectal malignancies, existing metastatic disease, or contraindications for MRI will not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could lead to earlier diagnosis and treatment of liver metastases in colorectal cancer patients, potentially improving survival outcomes.
How similar studies have performed: Other studies have shown promise in using advanced imaging techniques like DW-MRI for detecting metastases, suggesting potential success for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Have a high risk primary colorectal malignancy 2. Have a negative CT or includes no confirmatory evidence of liver metastases 3. Is able to undergo treatment if liver metastasis is found 4. Have provided written informed consent to participate in the study 5. Be aged 16 years or over Exclusion Criteria: 1. Have had a previous colorectal malignancy 2. Have metastatic disease 3. Have a synchronous second malignancy 4. Are contraindicated for MRI 5. Has a T3b or below low rectal tumour without EMVI or N1c
Where this trial is running
Macclesfield, Cheshire and 12 other locations
- Macclesfield District General Hospital — Macclesfield, Cheshire, United Kingdom (Recruiting)
- Queen's Hospital — Burton-on-Trent, Derbyshire, United Kingdom (Not_yet_recruiting)
- Broomfield Hospital — Chelmsford, Essex, United Kingdom (Recruiting)
- Royal Bolton Hospital — Bolton, Greater Manchester, United Kingdom (Recruiting)
- Medway Maritime Hospital — Gillingham, Kent, United Kingdom (Recruiting)
- University Hospital of South Manchester & Manchester Royal Infirmary — Wythenshawe, Manchester, United Kingdom (Recruiting)
- Royal Liverpool Hospital — Liverpool, Merseyside, United Kingdom (Recruiting)
- Royal Stoke University Hospital — Stoke-on-Trent, Staffordshire, United Kingdom (Recruiting)
- Royal Marsden Hospital — Sutton, Surrey, United Kingdom (Recruiting)
- Royal Gwent Hospital — Newport, Wales, United Kingdom (Recruiting)
- George Eliot Hospital — Nuneaton, Warwickshire, United Kingdom (Recruiting)
- Salisbury District Hospital — Salisbury, Wiltshire, United Kingdom (Recruiting)
- Queen Alexandra Hospital — Portsmouth, United Kingdom (Recruiting)
Study contacts
- Principal investigator: Gina Brown — Imperial College London
- Study coordinator: Caroline Martin
- Email: c.martin1@imperial.ac.uk
- Phone: +44 (0) 7749 655 817
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.