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Randomized contorol trial of transarterial chemoinfusion with cisplatin-lipiodol susupension or miriplatin-lipiodol suspension for advanced HCC

Not Applicable
Conditions
Hepatocellular carcinoma
Registration Number
JPRN-UMIN000003452
Lead Sponsor
First Department of Internal Medicine,Gifu University Hospital
Brief Summary

The 1-year survival rates in the cisplatin and miriplatin groups were 84.0% and 77.7%, and the 2-year survival rates were 60.0% and 51.8% respectively. (P = 0.905).The 1-year survival rates in the cisplatin and miriplatin groups with TAI alone were 71.4% and 71.4%, and the 2-year survival rates cannot be calculated yet. (P = 0.695).TE evaluation, the 1-year survival rates in TE3+4 and TE1+2 groups were 100% and 62.1%, and the 2-year survival rates were 66.7% and 33.1% respectively. (P = 0.0263).

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
98
Inclusion Criteria

Not provided

Exclusion Criteria

1)Patienta with sever co-morbidity such as cardiac failure or renal failure 2)Patienta with a medical history of severe hypersensitivity 3)Patients who are pregnant,lactating or are suspected to be a pregnant 4)Patients who are concluded to be inappropriate to participate in this study by their physitians

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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