ctDNA blood test to spot buried cancer after surgery or treatment in colorectal cancer
Official title: Monitoring of Minimal Residual Disease (MRD) in Selected Patients With Colorectal Cancer (Stages II-IV) Using Analysis of Circulating Tumor DNA (ctDNA) by the ddPCR Method
Run by Masaryk Memorial Cancer Institute · NCT07895459 · Data updated 2026-11-12
A blood test that looks for specific KRAS mutations in circulating tumor DNA to see if colorectal cancer has left residual disease or is likely to relapse.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 60 (estimated) |
| Sponsor | Masaryk Memorial Cancer Institute Academic / other |
| Locations | 1 site (Brno, Czech Republic) |
| Status | Recruiting |
| Started | February 7, 2023 |
| Main results expected | January 2027 |
| Study ends | September 2027 |
| Registry record updated | October 28, 2026 |
| Trial ID | NCT07895459 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults with histologically confirmed colorectal cancer (stages II–IV) who harbor KRAS G12 or G13 mutations and are scheduled for standard treatment.
✕Probably not a fit
Patients without the target KRAS mutations or who do not maintain regular blood sampling may not benefit from this approach.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study tests whether analyzing circulating tumor DNA in blood can detect minimal residual disease in colorectal cancer patients after surgery or treatment. The approach uses ddPCR to target KRAS G12 and G13 mutations and monitors patients over two years with regular blood draws. It aims to improve risk stratification and guide follow-up or therapy decisions based on MRD status. The study is prospective and conducted at Masaryk Memorial Cancer Institute in the Czech Republic. Primary outcome is early detection of recurrence and better prediction of disease course.
Why it matters
Potential benefit: If successful, patients could receive earlier intervention or closer monitoring based on MRD status.
How similar studies have gone: Prior studies using ctDNA for MRD in colorectal cancer have shown promise for early relapse detection, though approaches and mutation targets vary.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Histologically confirmed diagnosis of colorectal cancer (clinical stage II, III, or IV). * Presence of KRAS gene mutation (specifically G12 or G13 mutations) confirmed in the primary tumor tissue. * Age 18 years or older at the time of inclusion. * Patient scheduled for standard primary surgical resection, local treatment, or adjuvant therapy as per institutional guidelines. * Signed written informed consent to participate in the study. Exclusion Criteria: * Absence of target KRAS mutations (G12/G13) in the primary tumor. * Inability or unwillingness to comply with scheduled blood sampling and follow-up visits. * Active second primary malignancy that could interfere with ctDNA interpretation.
Where it's running
-
Masaryk Memorial Cancer Institute
Brno, Czech Republic, Czechia Recruiting
Study contacts
- Study coordinator: Igor Kiss, doc. MUDr. Ph.D., MBA
- Email: igor.kiss@mou.cz
- Phone: +42054313111
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.