Using MRI to Improve Treatment for Sigmoid Colon Cancer
Improving Radical Treatment Through MRI Evaluation of Pelvic Sigmoid Cancers
This study is testing if using MRI scans can help doctors plan better treatments for patients with sigmoid colon cancer compared to regular CT scans.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 244 (estimated) |
| Ages | 16 Years and up |
| Sex | All |
| Sponsor | Imperial College London Academic / other |
| Locations | 16 sites (Huntingdon, Cambridgeshire and 15 other locations) |
| Trial ID | NCT02222844 on ClinicalTrials.gov |
What this trial studies
This trial evaluates whether MRI imaging can enhance the treatment planning for patients with suspected or confirmed sigmoid colon adenocarcinoma who are eligible for curative treatment. Participants are randomly assigned to either a control group receiving standard preoperative CT imaging or an intervention group that includes MRI imaging. The study aims to determine if MRI can identify high-risk tumors more effectively than CT, potentially altering treatment plans based on additional diagnostic information. Patients will be followed up at 1 and 3 years to assess outcomes and quality of life.
Who should consider this trial
Good fit: Ideal candidates are individuals aged 16 and over with suspected or proven sigmoid colon adenocarcinoma who are eligible for curative treatment.
Not a fit: Patients with metastatic disease, contraindications for MRI, or severe co-morbidities may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could lead to more personalized and effective treatment plans for patients with sigmoid colon cancer.
How similar studies have performed: Other studies have shown that advanced imaging techniques like MRI can improve treatment outcomes in various cancers, suggesting a promising avenue for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Have a suspected or proven sigmoid colon adenocarcinoma 2. Is eligible for curative treatment 3. Has no irresectable metastatic disease 4. MRI can be reviewed by an MDT prior to surgery 5. Has no decision regarding radical treatment 6. Have provided written informed consent to participate in the study 7. Be aged 16 years or over Exclusion Criteria: 1. Have metastatic disease (including resectable liver metastases) 2. Have a synchronous second malignancy 3. Are contraindicated for MRI 4. Are contraindicated for or have allergy to Buscopan (e.g. glaucoma, small or large bowel obstruction, GFR\<30) 5. Have severe co-morbidities or previous medical history that prevent the application of eventual chemo/radiotherapy
Where this trial is running
Huntingdon, Cambridgeshire and 15 other locations
- Hinchingbrooke Hospital — Huntingdon, Cambridgeshire, United Kingdom (Recruiting)
- Leighton Hospital — Crewe, Cheshire, United Kingdom (Recruiting)
- University Hospital of North Tees — Stockton-on-Tees, County Durham, United Kingdom (Recruiting)
- Croydon University Hospital — Thornton Heath, Croydon, United Kingdom (Recruiting)
- Chesterfield Royal — Chesterfield, Derbyshire, United Kingdom (Recruiting)
- Queen Alexandra Hospital — Portsmouth, Hampshire, United Kingdom (Recruiting)
- St Mark's Hospital — Middlesex, Harrow, United Kingdom (Recruiting)
- Maidstone Hospital — Maidstone, Kent, United Kingdom (Recruiting)
- Queen Elizabeth the Queen Mother Hospital — Margate, Kent, United Kingdom (Recruiting)
- North Manchester General Hospital — Crumpsall, Manchester, United Kingdom (Recruiting)
- University Hospital of South Manchester & Manchester Royal Infirmary — Wythenshawe, Manchester, United Kingdom (Recruiting)
- Harrogate District Hospital — Harrogate, North Yorkshire, United Kingdom (Recruiting)
- Musgrove Park Hospital — Taunton, Somerset, United Kingdom (Recruiting)
- Yeovil District Hospital — Yeovil, Somerset, United Kingdom (Active_not_recruiting)
- Royal Marsden Hospital — Sutton, Surrey, United Kingdom (Recruiting)
- Salisbury District Hospital — Salisbury, Whiltshire, 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.