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Spots Global Cancer Trial Database for Follow-Up Study of Patients Who Have Undergone Surgery for Stage I, Stage II, or Stage III Colorectal Cancer

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Trial Identification

Brief Title: Follow-Up Study of Patients Who Have Undergone Surgery for Stage I, Stage II, or Stage III Colorectal Cancer

Official Title: A Randomised Controlled Trial to Assess the Cost-effectiveness of Intensive Versus no Scheduled Follow-up in Patients Who Have Undergone Resection for Colorectal Cancer With Curative Intent. (FACS - Follow-up After Colorectal Surgery)

Study ID: NCT00560365

Study Description

Brief Summary: RATIONALE: Following patients who have undergone surgery for colorectal cancer may help doctors learn more about the disease and plan better follow-up care. PURPOSE: This randomized clinical trial is following patients who have undergone surgery for stage I, stage II, or stage III colorectal cancer.

Detailed Description: OBJECTIVES: Primary * To assess the effect of augmenting symptomatic follow-up in primary care with two intensive methods of follow-up (monitoring tumor marker in primary care and intensive imaging in hospital) on survival of patients with stage I, II, or III colorectal cancer who have undergone curative resection. Secondary * Determine the quality of life of these patients. * Determine the cost of National Health Service (NHS) services utilized. * Determine the NHS cost per life-year saved. OUTLINE: This is a multicenter study. Patients are stratified according to certainty of need for imaging follow-up, as determined by the local clinician (uncertain vs certain). Patients are randomized to 1 of 4 follow-up arms. * Arm I (primary care follow-up): Patients undergo symptomatic follow-up (i.e., are asked to contact their physician if they have symptoms suggestive of disease recurrence). Some patients may also undergo a single CT scan 12-18 months post-randomization. * Arm II (primary care follow-up): Patients undergo tumor marker measurements (CEA) at baseline, every 3 months for 2 years, and every 6 months for 3 years. Some patients may also undergo a single CT scan 12-18 months post-randomization. * Arm III (intensive hospital follow-up): Patients undergo CT scan or MRI at baseline, every 6 months for 2 years, and then annually for 3 years. * Arm IV (primary care and intensive hospital follow-up): Patients undergo primary care and intensive hospital follow-up as in arms II (without the single CT scan) and III. All patients receive a handbook from their physician detailing possible symptoms suggestive of disease recurrence. Quality of life is assessed at baseline and then annually for 5 years.

Eligibility

Minimum Age: 50 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Queen's Hospital, Burton-upon-Trent, England, United Kingdom

Cumberland Infirmary, Carlisle, England, United Kingdom

Saint Richards Hospital, Chichester, England, United Kingdom

Queen Alexandra Hospital, Cosham, England, United Kingdom

Castle Hill Hospital, Cottingham, England, United Kingdom

Mid Cheshire Hospitals Trust- Leighton Hopsital, Crewe, England, United Kingdom

Mayday University Hospital, Croydon, England, United Kingdom

Darent Valley Hospital, Dartford Kent, England, United Kingdom

Royal Derby Hospital, Derby, England, United Kingdom

Russells Hall Hospital, Dudley, England, United Kingdom

Grantham and District Hospital, Grantham, Lincolnshire, England, United Kingdom

Harrogate District Hospital, Harrogate, England, United Kingdom

St. Mark's Hospital, Harrow, England, United Kingdom

Wycombe General Hospital, High Wycombe, England, United Kingdom

Hinchingbrooke Hospital, Huntingdon, England, United Kingdom

West Middlesex University Hospital, Isleworth, England, United Kingdom

Leeds General Infirmary, Leeds, England, United Kingdom

Charing Cross Hospital, London, England, United Kingdom

Mid Kent Oncology Centre at Maidstone Hospital, Maidstone, England, United Kingdom

Queen's Medical Centre, Nottingham, England, United Kingdom

Derriford Hospital, Plymouth, England, United Kingdom

Scarborough General Hospital, Scarborough, England, United Kingdom

Royal Shrewsbury Hospital, Shrewsbury, England, United Kingdom

Wexham Park Hospital, Slough, Berkshire, England, United Kingdom

Solihull Hospital, Solihull, England, United Kingdom

Southampton General Hospital, Southampton, England, United Kingdom

St. Peter's Hospital, Surrey, England, United Kingdom

Royal Cornwall Hospital, Truro, Cornwall, England, United Kingdom

Hillingdon Hospital, Uxbridge, England, United Kingdom

Warrington Hospital NHS Trust, Warrington, England, United Kingdom

Worcester Royal Hospital, Worcester, England, United Kingdom

Contact Details

Name: John N. Primrose, MD

Affiliation: University Hospital Southampton NHS Foundation Trust

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

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