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NCT06227728Recruiting

Analysis of PD-L1, TMB, MSI and ctDNA Dynamics to Predict and Monitor Response to Immunotherapy in Metastatic Cancer.

Analysis of PD-L1, TMB, CTDNA in Immunotherapy Response Monitoring and Prediction in Advancer Lung Cancer Treatment.

Source: ClinicalTrials.gov · Last updated 16 Jan 2026

Brief summary (registry, in English)

This is an observational clinical trial, aiming to investigate whether the ctDNA dynamics could predict early response to ICIs in patients with advanced-stage cancer. Moreover, conventional tumor markers PD-L1, TMB and MSI are to be investigated for their combined prognostic values in ICI treatment.

Status (registry)
Recruiting
Study type
Observational
Enrollment
50 (estimated)
First submitted
18 Jan 2024
Start date
22 Mar 2024
Primary completion date
1 Dec 2026
Lead sponsor
Gene Solutions
NCT number
NCT06227728

What you commit to

  • Study type: Observational
  • Planned participants: 50
  • From 22 Mar 2024 to the primary completion date, 1 Dec 2026
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients already started chemotherapy before enrollment.

Other illness

  • Medical or psychiatric conditions or occupational responsibilities that may preclude compliance with the protocol.

Other

  • Patients already started ICI before enrollment.
  • Consolidation ICI (eg. Durvalumab).
  • Patients did not agree to participate in the studies.

Who the study is looking for

  • 18 years and older, both genders.
  • Patients are diagnosed with stage IV cancer (lung, colorectal, breast, liver, gastric…) and indicated for ICI (first or second line). Concurrent chemotherapy with ICI is allowed.
  • FFPE/FNA sample is available.
  • Compliant with treatment protocol.
  • Patients consented to participate in the study.

Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Medicine and Pharmacy at HCMC
Coordinator of this site? Confirm its status
Ho Chi Minh CityVietnamRecruiting
Medical Genetics Institute
Coordinator of this site? Confirm its status
Ho Chi Minh CityVietnamNot yet recruiting

This page is information, not medical advice. Discuss any trial with your doctor.