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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
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.
Minimum Age: 50 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
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
Name: John N. Primrose, MD
Affiliation: University Hospital Southampton NHS Foundation Trust
Role: STUDY_CHAIR