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The aim of this study is to evaluate the 131I-chTNT-1/B treatment effect and safety of individual therapy using randomized controlled study, in order to acquire the evidence of evidence-based medicine and create a new program of targeted internal radiation therapy in advanced HCC patients.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| transcatheter arterial chemoembolization | Active Comparator | Patients will be treated with TACE only. |
|
| internal radiation group | Experimental | Patients will be treated with TACE combined with internal radiation. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| 131I-chTNT-1/B | Biological | 29.6 MBq/kg,intravenous administration in 1 hour,1-3 course of treatment |
|
| Measure | Description | Time Frame |
|---|---|---|
| Overall Survival | 3 years |
| Measure | Description | Time Frame |
|---|---|---|
| Time to Progression | 3 years |
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Inclusion Criteria:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Eastern hepatobilliary surgery hospital | Shanghai | Shanghai Municipality | 200438 | China |
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| ID | Term |
|---|---|
| C576180 | 131I-chimeric TNT-1-B monoclonal antibody |
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