Clinical trial · Observational
Dynamic ctDNA Detection for Colorectal Cancer Liver Metastases
Dynamic ctDNA Detection for Guiding Adjuvant Therapy and Recurrence Monitoring After Curative Resection of Colorectal Cancer Liver Metastases: A Prospective Study
NCT06404593CI-TRIAL-00076881completedClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Evaluating the value of dynamic monitoring of a colorectal cancer liver metastasis cohort underwent curative resection after receiving multipoint ctDNA detecting in predicting recurrence prognosis and guiding adjuvant chemotherapy treatment.
Conditions
Conditions (5)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Circulating Tumor DNA | — | UNRESOLVED | — |
| Colorectal Cancer | Malignant Colorectal Neoplasm | CURATED_BROADER | 0.80 |
| Liver Metastases | — | UNRESOLVED | — |
| Minimal Residual Disease | — | UNRESOLVED | — |
| Surgery | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Blood sampling | Diagnostic Test | — | UNRESOLVED |
Design
Arms and outcomes
Arms (5)
- label
- Group 1
- description
- Blood sampling 7 days after surgery
- interventionNames
- Diagnostic Test: Blood sampling
- label
- Group 2
- description
- Blood sampling 1 month after surgery
- interventionNames
- Diagnostic Test: Blood sampling
- label
- Group 3
- description
- Blood sampling 3 to 6 months after surgery
- interventionNames
- Diagnostic Test: Blood sampling
- label
- Group 4
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 20 Years
- Maximum age
- 85 Years
Show eligibility criteria text
Inclusion Criteria: 1. Before implementing any trial-related procedures, written informed consent should be signed; 2. \>=20 and \<= 85 years old, male or female; 3. Patients with liver metastases pathologically confirmed as colorectal adenocarcinoma; 4. According to the Response Evaluation Criteria for Solid Tumors (RECIST version 1.1), there is at least one lesion that can be measured by imaging; 5. The multidisciplinary team (MDT) confirmed that the liver metastases were initially resectable ,without locally treatable extrahepatic metastases; 6. The general physical condition is good (ECOG score 0-1); 7. Life expectancy of more than 3 months; 8. There is no obvious symptoms of primary bleeding, obstruction and other indications for emergency surgery; 9. adequate organ function; 10. samples meet NGS quality control requirements; 11. The subjects are able and willing to comply with the visits, treatment plans, laboratory tests and other research-related procedures stipulated in the research protocol. Exclusion Criteria: 1. Patients who are intolerant to systemic chemotherapy or surgery; 2. Patients with multiple primary lesions; 3. Blood samples and/or baseline tissue samples that do not meet the requirements for testing (hemolysis, low tumor cell content, insufficient DNA extraction yield, etc.); 4. Excessive tissue necrosis after conversion therapy, making it impossible to sample according to testing requirements 5. Patients who have not undergone surgery after conversion therapy, only receiving radiofrequency ablation or chemotherapy follow-up 6. Not all metastatic lesions were resected after conversion therapy, or liver metastatic lesions did not achieve R0 resection 7. No definite mutations detected in the tissue, or mutations detected in tumor tissue were not covered by the designed small panel.
References
Publications (0)
Data not yet available
No reference posted for this study.