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Prospective observational study to investigate the predictive factors on the efficacy of molecular targeting therapy for unresectable advanced hepatocellular carcinoma.

Not Applicable
Conditions
hepatocellular carcinoma
Registration Number
JPRN-UMIN000010000
Lead Sponsor
Japanese Red Cross Liver Study Group
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
150
Inclusion Criteria

Not provided

Exclusion Criteria

Patients with Eastern Cooperative Oncology Group (ECOG) performance status of 3 or 4 and pretreatment Child-Pugh score of 8 or more.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The clinicopathological factors related to time to progression of unresectable advanced hepatocellular carcinoma.patients treated with sorafenib.
Secondary Outcome Measures
NameTimeMethod
The clinicopathological factors related to overall survival of unresectable advanced hepatocellular carcinoma patients treated with sorafenib. The clinicopathological factors to predict serious adverse effects caused by sorafenib.
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