Carcinoma, Hepatocellular Clinical Trial
— HR-HCC/PHTOfficial title:
Hepatic Resection Versus Radiofrequency Ablation for Patients With Hepatocellular Carcinoma and Portal Hypertension
The purpose of the investigators' study is to prospectively compare the safety and efficacy of hepatic resection to radiofrequency ablation for hepatocellular carcinoma in patients with portal hypertension.
Status | Recruiting |
Enrollment | 120 |
Est. completion date | December 2022 |
Est. primary completion date | August 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 75 Years |
Eligibility | Inclusion Criteria: - Age 18-75 years - In the HR group, clinical diagnosis of HCC was confirmed by histopathological examination of surgical samples in all patients; in the RFA group, HCC diagnosis was confirmed by two types of clinical imaging (ultrasonography, computed tomography, or magnetic resonance imaging), togetherwith a serum level of a-fetoprotein higher than 400 ng/mL. If diagnosis based on imaging anda-fetoprotein level was uncertain, needle biopsy was performed. - Tumor stage fitted into Milan Criteria - Patients with clinically relevant portal hypertension, which is defined as the presence of esophageal varices and/or a platelet count of less than 100 000 per µL in association with splenomegaly. - Patients have Child-Pugh A or B liver function - No previous neoadjuvant treatment - No evidence of metastasis to the lymph nodes and/or distant metastases on the basis of preoperative imaging results and perioperative findings - No malignancy other than HCC for 5 years prior to the initial HCC treatment Exclusion Criteria: - History of cardiac disease - Known history of human immunodeficiency virus (HIV) infection - Known Central Nervous System tumors including metastatic brain disease - History of organ allograft - Substance abuse, medical, psychological or social conditions that may interfere with the patient's participation in the study or evaluation of the study results - Any condition that is unstable or which could jeopardize the safety of the patient and his/her compliance in the study - Pregnant or breast-feeding patients. |
Country | Name | City | State |
---|---|---|---|
China | Department of Hepatobilliary Surgery, Affiliated Tumor of Guangxi University | Nanning | Guangxi |
Lead Sponsor | Collaborator |
---|---|
Guangxi Medical University |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Overall survival | 3 years | ||
Primary | Hospital mortality | 90 day | ||
Secondary | Recurrence rate | 3 years |
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