Prediction of Hepatocellular Carcinoma Recurrence After Curative Treatment by Longitudinal Monitoring MRD Based on ctDNA

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-75
SponsorZhujiang Hospital

About this trial

This study will conduct a prospective cohort study to verify the predictive value of ctDNA-MRD longitudinal monitoring model in predicting postoperative recurrence, verify whether ctDNA-MRD longitudinal monitoring model can indicate recurrence earlier than imaging examination, and explore the feasibility of guiding adjuvant therapy after curative treatment based on this model.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Male or female patients aged 18-75 years;

Preoperative imaging examination diagnosed hepatocellular carcinoma (BCLC) stage 0 / stage A/stage B, eligible for radical surgery;

ECOG physical status score is 0-1;

Child-Pugh score is 5-6 points (Level A);

Disqualifiers

Patient can't provide blood samples for ctDNA testing;

Patient with two or more types of tumors at the same time;

Non-primary liver lesions;

Pregnant or lactating women;

Trial population

Patient with hepatocellular carcinoma who can undergo radical surgical resection

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • circulating tumor DNA

    Diagnostic test

    blood sample and tissue specimen for circulating tumor DNA will be done to patient with hepatocellular carcinoma

Treatment groups

255 Participants
are divided into 1 treatment group
Group A: Patient with hepatocellular carcinoma1 intervention

Trial outcomes

Primary outcomes

1

2-year recurrence-free survival rate

percentage of recurrence-free survival 2 years after surgery

Time frame
2 years

Secondary outcomes

1

Correlation between ctDNA-MRD status dynamic changes and relapse

Correlation between ctDNA-MRD status dynamic changes and relapse

Time frame
2 years

Other outcomes

Sponsors and contacts

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