RecruitingNot ApplicableNCT02704520

Magnetic Resonance Tumour Regression Grade (mrTRG) as a Novel Biomarker - Phase III Non CTIMP Trial

Magnetic Resonance Tumour Regression Grade (mrTRG) as a Novel Biomarker to Stratify Management of Good and Poor Responders to Radiotherapy: A Rectal Cancer Multicentre Randomised Control Trial to Avoid Surgery With 'Watch and Wait' or Intensify Treatment According to mrTRG


Sponsor

Imperial College London

Enrollment

441 participants

Start Date

Mar 1, 2016

Study Type

INTERVENTIONAL

Conditions

Summary

Open to patients undergoing any pre-operative treatment for locally advanced rectal cancer, TRIGGER is the only phase III clinical trial in the UK offering watch and wait. All patients will have post treatment MRI scans routinely performed, no change from the MERCURY trials high resolution MRI protocol is required. Patients will be randomised to either the control arm for management according to national guidelines - conventional MDT, clinical assessment post-treatment planning using the baseline MRI. Patients in the interventional arm will have their post treatment MRI scans read by a radiologist trained and supported to reliably report the mrTRG grade and have their management directed accordingly - 'Good response' (mrTRG 1\&2) - watch and wait (avoidance of surgery) offered. 'Poor response' (mrTRG 3-5) - local colorectal MDT is informed and uses information to discuss and agree next steps in treatment and surveillance. Patients are followed up for five years with QoL questionnaires completed at registration, 3 and 5 years.


Eligibility

Min Age: 16 Years

Plain Language Summary

Simplified for easier understanding

This study is testing whether a measure called Magnetic Resonance Tumor Regression Grade (mrTRG) — which looks at how well a rectal tumor has responded to pre-surgery treatment on an MRI scan — can accurately predict surgical and long-term outcomes in patients with rectal cancer. **You may be eligible if...** - You have been diagnosed with rectal cancer - You have received pre-surgery (neoadjuvant) chemotherapy and radiation therapy - You are scheduled for surgery to remove the tumor - You have had or will have an MRI scan of the rectum after completing pre-surgery treatment **You may NOT be eligible if...** - You have not received pre-surgery treatment - You are not scheduled for surgical removal of the tumor - You have metastatic rectal cancer (cancer that has spread to other organs) - Your MRI images are of insufficient quality to assess tumor response Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DIAGNOSTIC_TESTHigh resolution MRI scan

MRI reporting of tumour but not mrTRG in the control arm = standard of care

DIAGNOSTIC_TESTmrTRG assessment

Watch and wait offered for good responders Consider further treatment for poor responders


Locations(10)

Aberdeen Royal Infirmary - NHS Grampion

Aberdeen, Aberdeenshire, United Kingdom

Hampshire Hospitals NHS Foundation Trust

Basingstoke, Hampshire, United Kingdom

University Hospital of North Midlands NHS Trust - Royal Stoke

Stoke-on-Trent, Staffordshire, United Kingdom

Salisbury NHS Foundation Trust

Salisbury, Wiltshire, United Kingdom

Bristol Royal Infirmary

Bristol, United Kingdom

Colchester General Hospital

Colchester, United Kingdom

NHS Lanarkshire - Hairmyres Hospital

East Kilbride, United Kingdom

Diana Princess of Wales Hospital

Grimsby, United Kingdom

University Hospital of North Tees

Stockton-on-Tees, United Kingdom

Royal Marsden NHS Foundation Trust

Sutton, United Kingdom

View Full Details on ClinicalTrials.gov

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NCT02704520


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