Clinical trial Recruiting at 1 site Interventional Ages 18 and up

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.

More Colorectal Neoplasms trials

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment60 (estimated)
SponsorMasaryk Memorial Cancer Institute
Academic / other
Locations1 site (Brno, Czech Republic)
StatusRecruiting
StartedFebruary 7, 2023
Main results expectedJanuary 2027
Study endsSeptember 2027
Registry record updatedOctober 28, 2026
Trial IDNCT07895459 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

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.