Actively Recruiting
CyberKnife Stereotactic Body Radiation Therapy for Small Hepatocellular Carcinoma Patients With Decompensated Cirrhosis
Led by Beijing 302 Hospital · Updated on 2023-06-27
60
Participants Needed
1
Research Sites
315 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The aim of our research is to evaluate the curative effect and safety of CyberKnife stereotactic body radiation therapy in treating small hepatocellular carcinoma (HCC) patients with decompensated cirrhosis.
CONDITIONS
Official Title
CyberKnife Stereotactic Body Radiation Therapy for Small Hepatocellular Carcinoma Patients With Decompensated Cirrhosis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Primary hepatocellular carcinoma diagnosed by a surgeon, radiologist, or oncologist according to international guidelines or pathology
- Unable or unwilling to undergo other treatments
- Residual normal liver volume of at least 700 cc
- Decompensated cirrhosis (Child-Pugh B or C classification)
- No portal vein tumor thrombus
- Eastern Cooperative Oncology Group (ECOG) score of 0 or 1
- Tumor located more than 5 mm away from esophagus, stomach, duodenum, and bowel
- Rejecting other therapies such as resection or liver transplantation
- Platelet count of 50 x 10^9/L or higher and white blood count of 1.5 x 10^9/L or higher
- Patients with hepatitis B treated with adefovir or entecavir, or patients with hepatitis C with negative HCV DNA
You will not qualify if you...
- Presence of tumor thrombus
- Presence of extrahepatic metastasis
- Presence of lymph node involvement
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Beijing 302 hospital
Beijing, China, 100039
Actively Recruiting
Research Team
J
Jing Sun
CONTACT
X
Xuezhang Duan
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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