NCT04103398CompletedPhase 3
TACE Plus Sorafenib Versus TACE Alone for Recurrent Intermediate Hepatocellular Carcinoma
TRansarterial ChEmoembolization Plus SorAfenib Versus Transarterial Chemoembolization Alone for Recurrent Intermediate Hepatocellular Carcinoma: A Phase 3, Open Label, Multicenter, Randomized Controlled Trial
Source: ClinicalTrials.gov · Last updated 28 Feb 2024
Brief summary (registry, in English)
The study is a multicenter phase III randomized trial. The purpose is to investigate both the efficacy and safety of transarterial chemoembolization (TACE) plus sorafenib versus TACE alone for recurrent intermediate hepatocellular carcinoma patients.
- Status (registry)
- Completed
- Phase (registry)
- Phase 3
- Study type
- Interventional
- Enrollment
- 162 (actual)
- First submitted
- 20 Sept 2019
- Start date
- 2 Oct 2019
- Primary completion date
- 31 Dec 2023
- Lead sponsor
- Sun Yat-sen University
- Diseases
- Liver and biliary tract cancer
- NCT number
- NCT04103398
What you commit to
- Study type: Interventional · Phase 3
- Participants enrolled: 162
- From 2 Oct 2019 to the primary completion date, 31 Dec 2023
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Unable to orally take drugs;
- Participating other clinical drug trials 12 months before enrolment.
Other illness
- Have a history of hepatic encephalopathy, refractory ascites, severe esophageal and gastric varices or variceal bleeding and obstructive jaundice;
- Allergic to intravenous contrast agents;
- Infection of HIV, known syphilis requiring treatment;
- Have a known history of prior invasive malignancies within 5 years before enrolment;
- Severe dysfunction involving heart, kidney or other organs;
- Severe active clinical infection which is over grade 2 based on NCI-CTC version 4;
- Patients with mental disorders which may impact informed consent;
Other
- Have lesions which are diffuse or can not be evaluated via imaging. Tumor burden\>50%;
- Have contraindications for TACE;
- Have metastasis in central nervous system;
- Pregnant or breastfeeding women, or expecting to conceive or father children within two years;
- Patients with allotransplantation;
Who the study is looking for
- Age: 18-75 years;
- Diagnosed as HCC based on the American Association for the Study of Liver Diseases 2018 Guideline on Liver Cancer Diagnosis;
- Initial tumor recurrence following curative surgical resection (R0 hepatectomy) (two to three lesions with at least one lesion \>3 cm in diameter or more than three lesions of any diameter). Tumor burden ≤ 50% and no distant metastasis and macroscopic vascular invasion;
- Histologically confirmed microvascular invasion in the specimen slices of surgically removed primary tumor;
- Eastern Cooperative Oncology Group scoring 0-1;
- Child-Pugh A class;
- At least 3 months of life expectancy;
- Adequate hematologic, hepatic and renal function: absolute neutrophil count ≥ 1.5x10\^9/L, platelet ≥ 60 x10\^9/L, Hb ≥ 90g/L, albumin ≥ 30g/L, total bilirubin ≤ 1.5 x upper limit of normal (ULN) , ALT \< 5×ULN, AST \< 5×ULN, alkaline phosphatase \< 4×ULN, extended prothrombin time not exceeding 6s of ULN, creatine\<1.5×ULN.
Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| the First Affiliated Hospital of Sun Yat-sen University Coordinator of this site? Confirm its status | Guangzhou | China | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.