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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05699746
Other study ID # IR2022577
Secondary ID
Status Not yet recruiting
Phase Phase 3
First received
Last updated
Start date March 2023
Est. completion date December 2026

Study information

Verified date January 2023
Source Zhejiang University
Contact Kefeng Ding, MD, PhD
Phone +8687784720
Email dingkefeng@zju.edu.cn
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Patients with stage Ⅰ colorectal cancer or stage Ⅱ colon cancer usually have a good prognosis and are not recommended to receive adjuvant chemotherapy after radical surgery. With the advances in liquid biopsy technology, detection of circulating tumor DNA (ctDNA) can effectively identify early-stage cancer patients with minimal residual disease (MRD) after surgery. According to the growing number of MRD studies in solid tumor, colorectal cancer patients with ctDNA-MRD detection have a poor clinical outcome and are likely to relapse within two years. This study aims to assess the efficacy of adjuvant chemotherapy with capecitabine plus oxaliplatin (CAPEOX) compared with conventional observation in MRD-positive patients with stage I colorectal cancer and clinically low-risk stage II colon cancer.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 38
Est. completion date December 2026
Est. primary completion date September 2026
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: 1. Colorectal cancer confirmed by pathology, and the TNM stage (AJCC v8) is stage I or stage II. Stage II patients have T3 colonic adenocarcinoma with proficient mismatch-repair system (by immunohistochemistry for four mismatch repair proteins MSH1, MSH2, MSH6, and PMS2) and have no the following clinical risk factors: a) less than 12 lymph nodes examined; b) mucinous carcinoma; c) poor differentiation; d) bowel obstruction or perforation; e) lymphatic/vascular invasion, perineural invasion; f) close, indeterminate, uncertain, positive margins 2. ECOG performance status 0-1 3. No neoadjuvant therapy before surgery 4. Appropriate for active surveillance (i.e., no adjuvant chemotherapy) based on current practice patterns or according to the Chinese Society of Clinical Oncology guidelines for Colorectal Cancer (version 2022) 5. No history of other primary cancers in the past 3 years 6. No history of bone marrow, stem cell or organ transplant 7. Blood samples from 7 to 21 days after surgery were tested positive for ctDNA (tested by MinerVa MRD assay) 8. Pregnancy test done within 14 days before randomization must be negative (for women of childbearing potential only) 9. Voluntarily join the study and sign the informed consent document 10. No unstable or any medical condition that affects patient safety and study compliance evaluated by researchers 11. Availability and provision of adequate surgical tumor tissue for molecular diagnostics Exclusion Criteria: 1. Patients with multiple primary colorectal cancers 2. Patients with another primary cancer 3. Patients have the following conditions by blood test, or have obvious contraindication in adjuvant chemotherapy: 1. Moderate/severe renal impairment (GFR<30 ml/min), as calculated by the Cockcroft and Gault equation 2. Absolute neutrophil count <1.5×109/L 3. Platelet count < 75×109/L 4. Hemoglobin <90 g/L 5. Aspartate aminotransferase/Alanine aminotransferase >2.5 × upper limit of normal 4. Lactating women 5. Have serious or uncontrolled medical condition that may preclude compliance with the protocol

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Capecitabine tablets
Capecitabine 1000 mg/m2, twice daily PO for 14 days, repeat every 3 weeks, for at most 8 cycles.
Oxaliplatin
Oxaliplatin 130 mg/m2 IV day 1, combined with Capecitabine, for at most 8 cycles.

Locations

Country Name City State
China Second Affiliated Hospital Zhejiang University College of Medicine Hangzhou Zhejiang
China Sir Run Run Shaw Hospital, Zhejiang University School of Medicine Hangzhou Zhejiang
China The second hospital of Ningbo City Ningbo Zhejiang
China Changhai Hospital of Shanghai Shanghai Shanghai

Sponsors (2)

Lead Sponsor Collaborator
Zhejiang University GeneCast Biotechnology Co., Ltd.

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Recurrence-free survival 18 months
Secondary Clearance of circulating tumor DNA (ctDNA) 6 months
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