Recurrent Liver Cancer: Reconceptualization and Reevaluation
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Recurrent Liver Cancer, Primary Liver Cancer. Basic parameters: 18 years — 75 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- China
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
The goal of this observational study is to determine if a specific protein can serve as a novel indicator for the recurrence of liver cancer. The study will focus on recurrent liver cancer patients and compare participants to primary liver cancer patients as controls. The primary purpose is to assess whether the elevated levels of this protein can be used to monitor the recurrence of liver cancer. The main questions it aims to answer are: Is the levels of the protein significantly elevated in recurrent liver cancer patients compared to primary liver cancer patients? Can the protein be used as a reliable biomarker for the early detection of liver cancer recurrence? Researchers will compare the protein levels in the following groups: 50 recurrent liver cancer patients (training set) with abnormally high levels of the protein. 250 recurrent liver cancer patients (validation set) to confirm the protein's elevation in a separate cohort. Participants will be required to: * Provide blood samples for protein analysis. * Undergo regular follow-up visits for monitoring and data collection. * Allow access to their medical records for relevant clinical information.
Detailed description
As part of the patient registry, investigators will implement the following registration procedures and other quality factors:
Screening and Recruitment: Eligible patients will be screened and recruited through hospital liver cancer outpatient clinics and wards. Patients must meet the diagnostic criteria for recurrent or primary liver cancer and be willing to participate in the study.
Data Collection: Clinical information of participants will be collected, including demographic characteristics, medical history, treatment regimens, and follow-up outcomes. Data will be entered and verified by professionals to ensure accuracy and completeness.
Quality Control: Strict quality control measures will be implemented, including data audits, sample management, and laboratory testing. Regular reviews and validations of the data will be conducted to ensure the reliability and replicability of the study results.
Data Security: The privacy and personal information of participants will be protected. All data will be stored in a secure environment and comply with relevant laws, regulations, and ethical guidelines.
Ethical Review: The research protocol has been approved by the ethics committee, ensuring that the conduct of the study meets ethical standards and the protection of patient rights.
Primary outcome measures
- Sensitivity and Specificity of the Novel Protein Indicator [Time frame: Assessed at the end of the study (up to 3 years), once all patient data has been collected and analyzed.]
- Positive and Negative Predictive Values [Time frame: Calculated after the threshold value has been determined and applied to the patient data (up to 3 years).]
Secondary outcome measures (4)
- Overall Survival (OS) [Time frame: Monitored throughout the study and reported at 1 year, 2 years, and study completion (up to 5 years).]
- Progression-Free Survival (PFS) [Time frame: Assessed at each follow-up visit, every 3 months for the first 2 years, then every 6 months until study completion (up to 5 years).]
- Disease-Free Survival (DFS) [Time frame: Monitored and reported at 6 months, 1 year, 2 years, and study completion (up to 5 years).]
- Time to Progression (TTP) [Time frame: Measured from the initiation of the study intervention until progression or defined worsening, assessed at each follow-up visit (every 3 months for the first 2 years, then every 6 months until study completion, up to 5 years).]
Eligibility criteria
Inclusion criteria
- Diagnosed with primary hepatocellular carcinoma or diagnosed with non-HCC
- The patient or the patient's legal representative must be able to read, understand, and sign the informed consent form
- Agree to provide blood samples and have good clinical compliance
- Complete clinical basic information, including: the patient's unique traceability number (ID card number/outpatient number/health insurance card number), age, gender, imaging and/or pathological diagnosis results (for patients with primary liver disease), imaging examination confirmed heteromorphic liver cancer (for non-HCC patients)
Exclusion criteria
- Pregnant women
- Those who have received organ transplantation
- Non-HCC patients diagnosed with other tumors
- Patients with primary hepatocellular carcinoma complicated by other tumors
- Those judged by the researcher as not meeting the inclusion criteria
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Observational model
- Cohort
Study locations
China · 1 center
- The Second Affiliated Hospital of Nanjing Medical University — Nanjing
Identifiers
NCT: NCT06430983 · 2024KY16401