Overview

Microwave Ablation Combined With TACE in the Treatment of Unresectable Huge Hepatocellular Carcinoma Huge

Status:
Recruiting
Trial end date:
2021-12-30
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this study was to prospectively evaluate the efficacy and safety of TACE combined with MWA in patients with huge unresectable hepatocellular carcinoma.
Phase:
N/A
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Fan Weijun
Criteria
Inclusion Criteria:

1. The performance status of Eastern Cooperative Oncology Group (ECOG) must be 0-1

2. The diagnosis of primary hepatocellular carcinoma must be in line with the American
Society for the study of liver diseases (AASLD) diagnostic criteria for hepatocellular
carcinoma (HCC)

3. Child-Pugh score A or B;

4. Aged from 18 to 75 years;

5. Subjects voluntarily join the study, and signe informed consent;

6. No anti-tumor therapy was received;

7. Meet the following 4 characteristics: A. primary tumor diameter more than or equal to
10cm; B. no more than 3 HCC foci, and the maximum diameter is less than or equal to
5cm; C. with IIa, I or no portal vein tumor thrombus (Cheng's Classification);D. the
tumor could not be surgically removed

8. No extrahepatic metastases

Exclusion Criteria:

1. Abnormal coagulation function: PLT < 40×109/L, PTA < 40%;

2. Patients have the past history of liver cancer treatment, such as transplantation,
resection, radiotherapy, chemotherapy and so on;

3. Patients participated in clinical trials of equipment or drugs (signed informed
consent) within 4 weeks;

4. Patients accompany by ascites, hepatic encephalopathy and esophageal and gastric
varices bleeding;

5. Any serious accompanying disease, which is expected to have an unknown, impact on the
prognosis, include heart disease, inadequately controlled diabetes and psychiatric
disorders;

6. Patients accompanied with other tumors or past medical history of malignancy;

7. Pregnant or lactating patients, all patients participating in this trial must adopt
appropriate birth control measures during treatment;

8. Allergic to adriamycin chemotherapy drugs,contrast agent and lipiodol;

9. Patients have poor compliance.