Overview
Efficacy of Postoperative Adjuvant Chemotherapy for Stage II Colon Cancer With High Risk Factors(EPAC1)
Status:
Recruiting
Recruiting
Trial end date:
2024-07-31
2024-07-31
Target enrollment:
0
0
Participant gender:
All
All
Summary
The purpose of this study is to design a prospective randomized clinical trial to explore whether postoperative adjuvant chemotherapy may provide survival benefit for stage II colon cancer patients with high risk factors.Therefore the investigators can provide high level clinical evidence of indications for patients with colon cancer with stage II colon cancer.Phase:
Phase 3Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Beijing Cancer HospitalCollaborators:
Peking Union Medical College Hospital
Peking University People's HospitalTreatments:
Capecitabine
Oxaliplatin
Criteria
Inclusion Criteria:1. aged 18 to 75 years;
2. pathologically confirmed adenocarcinoma of the colon
3. after curative resection pathological stage was T3-4N0M0;
4. with at least one of the following factors:
1. T4 staging
2. lymph nodes number less than 12
3. poor differentiation (except MSI-H)
4. LVI or PNI
5. obstruction or perforation
6. Elevated preoperative serum CEA
5. ECOG Performance status 0-1
6. no evidence of distant metastases
7. no preoperative chemotherapy or chemoradiation therapy
8. ANC > 1.5 cells/mm3, HGB > 10.0 g/dL, PLT > 100,000/mm3, total bilirubin ≤ 1.5 xULN,
AST≤ 3 x ULN, ALT ≤ 3 x ULN.
9. Patients must read, agree to, and sign a statement of Informed Consent prior to
participation in this study.
Exclusion Criteria:
1. combined with other cancer
2. Creatinine level greater than 1.5 times the upper limit of normal.
3. Patients who have received preoperative chemotherapy or chemoradiotherapy.
4. Patients with a history of a prior malignancy within the past 5 years.
5. Women who are pregnant or breast-feeding.
6. patients may not complete the whole schedule of chemotherapy
7. Patients with any other concurrent medical or psychiatric condition or disease which
would make them inappropriate candidates for entry into this study.