Hepatocellular Carcinoma Clinical Trial
Official title:
Acquisition of Blood and Tumor Tissue Samples From Patients With Hepatobiliary Tumors
NCT number | NCT04445532 |
Other study ID # | JS-2296 |
Secondary ID | |
Status | Recruiting |
Phase | |
First received | |
Last updated | |
Start date | October 11, 2020 |
Est. completion date | June 1, 2025 |
Hepatobiliary tumors have a poor prognosis and high individual heterogeneity, so it is of great significance to find important prognostic markers and then screen out specific subgroups of people; meanwhile, chronic hepatitis, cirrhosis, and healthy control participants also need to show the evolution of tumors and discover specific diagnostic markers as a control group. Moreover, targeted therapy and immunotherapy make cancer treatment enter a new field, but only part of patients achieve response rates and reach clinical benefit. However, these drugs are expensive and can cause treatment-related adverse events. Therefore, reliable biomarkers identification is needed to help predict the response to these treatment options in order to screen patients with better responsiveness and avoid wasting money. Multi-omics research can reveal the characteristics of hepatobiliary tumors more deeply and find meaningful therapeutic targets. Therefore, 450 patients at least 18 years of age with hepatobiliary tumors were included in this study.
Status | Recruiting |
Enrollment | 450 |
Est. completion date | June 1, 2025 |
Est. primary completion date | June 1, 2025 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: 1. Be older than 18 years old; 2. ECOG 0-2 points; 3. May have received treatment; 4. Clinical consideration or diagnosis of benign and malignant hepatobiliary tumors; or chronic hepatitis, cirrhosis, or healthy control participants; 5. Patients may have received or are about to undergo surgery, chemotherapy, radiotherapy, targeted therapy, local therapy, immunotherapy, etc.; 6. Patients understand and are willing to sign written informed consent documents. Exclusion Criteria: 1. The doctor thinks it is not suitable to enter the group (mental disorder or poor compliance, etc.) 2. Pregnant women; 3. Active or uncontrollable infections (fungi, bacteria, etc.); 4. Estimated survival time <12 weeks; 5. If the patient is receiving chronic anticoagulant therapy, the anticoagulant withdrawal should not be shorter than 3 days; 6. In the evaluation of the doctor, there is a risk of uncontrolled complications in the biopsy. |
Country | Name | City | State |
---|---|---|---|
China | Chinese Academy of Medical Sciences & Peking Union Medical College Hospital | Beijing | Beijing |
Lead Sponsor | Collaborator |
---|---|
Peking Union Medical College Hospital | GeneCast Biotechnology Co., Ltd., Geneplus-Beijing Co. Ltd., OrigiMed, YuceBio Technology Co., Ltd. |
China,
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* Note: There are 23 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Collected samples | Collected normal tissue, tumor samples, blood, urine, feces, ascites, bile samples from patients with hepatobiliary cancers | through study completion, an average of 5 years | |
Secondary | Biomarkers of resectable disease-free recurrence (DFS) and overall survival (OS) | through study completion, an average of 5 years | ||
Secondary | Biomarkers of evolution of tumors and discover specific diagnostic markers for hepatobiliary tumors | through study completion, an average of 5 years | ||
Secondary | Biomarkers of the efficacy of target and immunotherapy for advanced hepatobiliary tumors | through study completion, an average of 5 years | ||
Secondary | Multi-omics analysis to further type and find therapeutic targets | through study completion, an average of 5 years |
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