An observational study in Hepatocellular Carcinoma, sponsored by Taipei Veterans General Hospital, Taiwan. Status unknown at 1 site in Taiwan. Open to participants aged 20 Years and older. Per ClinicalTrials.gov, last updated 2017-09-06.
Sponsored by Taipei Veterans General Hospital, Taiwan · Observational
The purpose of this multicenter registry is to gather the safety, efficacy and survival data in intermediate and advanced HCC patients treated drug-eluting microsphere in Taiwan in order to provide clinical evidence in HCC management to physicians in the region, and to support the application of deTACE in treating advanced HCC patients.
The purpose of this multicenter registry is to gather the safety, efficacy and survival data in intermediate and advanced HCC patients treated drug-eluting microsphere in Taiwan in order to provide clinical evidence on deTACE in HCC management to physicians in the region, and to support the application of in treating advanced HCC patients.
Primary Objective:
To collect 1-year overall survival of chemoembolization with drug-eluting microsphere in intermediate and advanced HCC patients in Taiwan.
Secondary Objectives:
Exploratory Objectives:
Superselective Drug-Eluting Chemoembolization in Unresectable Intermediate and Advanced HCC Patients.
Inclusion Criteria:Patients must meet all of the following inclusion criteria in order to be entered into the study:
Patient must have a diagnosis of hepatocellular cancer confirmed by AASLD and at least one of the following method:
Patient must not be suitable for treatment by resection or percutaneous ablation at time of study entry.
Patient MUST be with either BCLC stage B OR C, and meet the following criteria:
Exclusion Criteria:If patients meet any of the following criteria they may not be entered into the study:
Overall survival
To define all participants from the day of the first HepaSphere Treatment until end of study or death is reported, whichever comes first.
Time frame: 1 year
Tumor Response
Tumor response will be assessed using modified Response Evaluation Criteria In Solid Tumors (mRECIST) criteria to evaluate tumor necrosis under CT/ MRI and will be presented as %.
Time frame: 1 year
Adverse Event (AE)
Adverse event will be accessed according to CTCAE 4.0 after treatments until end of study or death.
Time frame: 1 year
Exploratory Objectives, Time-To-Progression (TTP)
To define all participants from the day of the first HepaSphere Treatment until tumor progression or death is first reported, whichever comes first.
Time frame: 1 year
Exploratory Objectives, Downstaging
Tumor staging will be accessed according to BCLC staging system and Milan criteria, and will be reviewed at follow-up until end of study or death.
Time frame: 1 year
This study is status unknown, as verified in Sep 2017. You cannot join it, but the record below documents what was studied.
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Taipei Veterans General Hospital, Taiwan