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Follow-Up Care With or Without CEA Assessments in Patients Who Have Undergone Surgery for Stage II or Stage III Colorectal Cancer

Follow-Up of Fully Resected Stage II or III Colorectal Cancer. Phase III Multicentric Prospective Randomised Study

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00995202
Acronym
SURVEILLANCE
Enrollment
1997
Registered
2009-10-15
Start date
2009-09-30
Completion date
2021-06-30
Last updated
2021-12-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colorectal Cancer

Keywords

stage II colon cancer, stage II rectal cancer, stage III colon cancer, stage III rectal cancer, adenocarcinoma of the colon, adenocarcinoma of the rectum

Brief summary

RATIONALE: Diagnostic procedures, such as ultrasound, x-ray, colonoscopy, CT scan, and CEA assessment, may help monitor a patient's response to surgery. It is not yet known which follow-up regimen is more effective in patients who have undergone surgery for colorectal cancer. PURPOSE: This randomized phase III trial is comparing two types of follow-up care with or without CEA assessments to see how well they work in patients who have undergone surgery for stage II or stage III colorectal cancer.

Detailed description

OBJECTIVES: * Evaluate the efficacy of reinforced versus standard follow-up care and the utility of follow-up CEA assessments in patients with fully resected stage II or III colorectal cancer. OUTLINE: This is a multinational/multicenter study. Patients are randomized to 1 of 2 follow-up arms. * Standard follow-up: Patients undergo clinical assessments every 3 months until year 3 and every 6 months until year 5. They are then assessed at least yearly thereafter. Patients undergo abdominal ultrasound every 3 months until year 3 and then every 6 months until year 5; chest x-ray every 6 months until year 3 and then annually until year 5; and colonoscopy at 3 years after surgery then every 3 to 6 years thereafter. * Reinforced follow-up: Patients undergo clinical assessments every 3 months until year 3 and every 6 months until year 5. They are then assessed at least yearly thereafter. Patients undergo alternate assessments every 3 months comprising thoraco-abdomino-pelvic CT scan or abdominal ultrasound until year 3 and then every 6 months until year 5. They also undergo colonoscopy at 3 years after surgery then every 3 to 6 years thereafter. Patients undergo a second randomization to 1 of 2 follow-up arms at the beginning of the study. * CEA measurement: Patients undergo measurement of CEA levels every 3 months until year 3, every 6 months until year 5, and at least yearly thereafter. * No CEA measurement: Patients do not undergo CEA measurement. Blood and tissue blocks of normal and tumor tissues are collected for the validation of protein serum, genetics, or immunologic markers predictive for relapse.

Interventions

PROCEDUREStandard Monitoring CEA

No specific follow-up of CEA

PROCEDUREIntensive Monitoring CEA

CEA levels are measured every 3 months for 3 years, then every 6 months for 2 years.

PROCEDUREStandard Monitoring Imagery

Abdominal ultrasound examination every 3 months during 3 years then every 6 months during 2 years then annually. Chest X-ray examination eveyr 6 months during 3 years then annually during 2 years

PROCEDUREIntensive Monitoring Imagery

Alternation every 3 months of TDM thoraco-abdomino-pelvis and abdominal ultrasound examination during 3 years and twice a year after during 2 years. Coloscopy at 3 years and then evry 5 years if normal

Sponsors

Federation Francophone de Cancerologie Digestive
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

This study is a surveillance study not an interventional study with products

Eligibility

Sex/Gender
ALL
Age
18 Years to 120 Years
Healthy volunteers
No

Inclusion criteria

DISEASE CHARACTERISTICS: * Pathologically confirmed adenocarcinoma of the colon or rectum * Stage II or III disease * No distant metastatic disease * Has undergone curative resection for no residual tumor * Carcinoembryonic antigen (CEA) ≤ 1.5 x upper limit of normal after surgery PATIENT CHARACTERISTICS: * WHO performance status 0-1 * Not pregnant or nursing * Fertile patients must use effective contraception * No inflammatory bowel disease * No other malignancy within the past 5 years except basal cell carcinoma of the skin and/or carcinoma in situ of the cervix * No genetic syndromes PRIOR CONCURRENT THERAPY: * See Disease Characteristics

Design outcomes

Primary

MeasureTime frameDescription
Overall survival rate5 yearsTime between randomization and date of death (all causes)

Secondary

MeasureTime frameDescription
Disease-free survival rate5 yearsTime between randomization and first recurrence (local or metastatic) or death (all causes)

Countries

Belgium, France, Martinique

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 10, 2026