Hepatocellular Carcinoma Clinical Trial
— TACEforHCCOfficial title:
The Efficacy, Safety, and Patient Reported Outcomes of Different Regimens of Transarterial Chemoembolization in Patients With Hepatocellular Carcinoma
| Verified date | December 2012 |
| Source | Sun Yat-sen University |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | China: Ministry of Health |
| Study type | Interventional |
The purpose of this study is to evaluate efficacy, safety, and patient reported outcomes (PRO) of different regimens of transarterial chemoembolization (TACE) in patients with hepatocellular carcinoma (HCC).
| Status | Completed |
| Enrollment | 365 |
| Est. completion date | December 2010 |
| Est. primary completion date | December 2010 |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 18 Years to 75 Years |
| Eligibility |
Inclusion Criteria: - Adult patients with minimal height of 150cm and minimal weight of 50 KG - Histological confirmed HCC - with no previous treatment - With unresectable tumor - With solitary or multiple intrahepatic tumor, the diameter of the largest one must larger than 7cm. - No significant baseline liver dysfunction. Cirrhotic status of Child-Pugh class A only - No significant renal impairment (creatinine clearance < 30 mL/minute) - The following laboratory parameters: - Platelet count = 60,000/µL - Hemoglobin = 8.5 g/dL - Total bilirubin = 1.5 mg/dL - ASL and AST = 5 x upper limit of normal - Serum albumin = 35 g/L - Serum creatinine = 1.5 x upper limit of normal - INR = 1.5 or a Pt/PTT within normal limits - Absolute neutrophil count (ANC) > 1,500/mm3 - Ability to understand the protocol and to agree to and sign a written informed consent document Exclusion Criteria: - Avascular tumor - Main portal vein obstruction without cavernous transformation - Evidence of hepatic decompensation including esophageal or gastric variceal bleeding or hepatic encephalopathy - Obstructive jaundice - Severe underlying cardiac or renal diseases - Known or suspected allergy to the investigational agent or any agent given in association with this trial - Pregnant or breast-feeding patients. - History of organ allograft - Active clinically serious infections - Any condition that is unstable or which could jeopardize the safety of the patient and his/her compliance in the study |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Factorial Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| China | Cancer Center Sun Yat-sen University | Guangzhou | Guangdong |
| Lead Sponsor | Collaborator |
|---|---|
| Sun Yat-sen University | Guangdong General Hospital, Kaiping Central Hospital, Ministry of Health, China, The 458 Hospital of Chinese PLA |
China,
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* Note: There are 28 references in all — Click here to view all references
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|---|---|---|---|---|
| Primary | Overall survival | 3 years | Yes | |
| Secondary | Time to progression | 3 years | Yes |
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