Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06098560

Circulating Tumor DNA (ctDNA) as a Predictive Biomarker for Immunotherapy in Advanced or Locally Advanced dMMR/MSI-H Colorectal Patients

Study on the Clinical Potential of Circulating Tumor DNA in Advanced or Locally Advanced dMMR/MSI-H Colorectal Patients Treated With Immunotherapy

Status
Recruiting
Phase
Study type
Observational
Enrollment
60 (estimated)
Sponsor
Geneplus-Beijing Co. Ltd. · Industry
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

dMMR/MSI-H colorectal cancer patients are the dominant population of immunotherapy/neoadjuvant immunotherapy, but imaging evaluation of immunotherapy efficacy is insufficient. There are some cases, although no disease remission was found on imaging,pathological complete response (pCR) was confirmed after surgery. Meanwhile,previous studies have shown that dynamic changes in ctDNA can help assess immunotherapy efficacy. Therefore, we propose to conduct a multicenter, prospective, observational clinical study to explore the efficacy prediction and monitoring value of ctDNA in immunotherapy for advanced or locally advanced dMMR/MSI-H colorectal cancer.

Conditions

Timeline

Start date
2023-10-30
Primary completion
2025-12-01
Completion
2025-12-01
First posted
2023-10-24
Last updated
2025-09-04

Locations

2 sites across 1 country: China

Source: ClinicalTrials.gov record NCT06098560. Inclusion in this directory is not an endorsement.