Chinese PLA General hospital
Beijing, None Selected, 100853, China
Location status: Recruiting
Location contact
Feng Duan, MD
CONTACT
Qunfang Zhou, MD
CONTACT
NCT Number: NCT06622031
Hepatocellular carcinoma (HCC) with main trunk portal vein tumor thrombus (PVTT) has poor prognosis. The main lethiferous factor is the upper gastrointestinal hemorrhage by PVTT-related portal hypertension, then the second is the tumor-caused death. It is vital to prevent the portal hypertension by PVTT.
Interested in participating?
Request Info18 year–75 year
All sexes
Interventional
Not applicable
Beijing, None Selected, 100853, China
Location status: Recruiting
Feng Duan, MD
CONTACT
Qunfang Zhou, MD
CONTACT
Portal hypertension by main trunk portal vein tumor thrombus (PVTT) is a severe disease. Patients usually die of gastrointestinal hemorrhage rather than tumor progression. It is vital to prevent the portal hypertension. Transjugular intrahepatic portosystemic shunt (TIPS) is an effective method to alleviate the portal pressure. Then the risk of gastrointestinal hemorrhage is decreased which provides an opportunity for system therapy. In this study, the investigators explore the TIPS combined with Lenvatinib and PD-1 inhibitor for advanced hepatocellular carcinoma with main trunk portal vein tumor thrombus. The investigators aim to add clinical evidence for this subtype of advanced HCC.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
A needle punctured the portal vein through the transjugular approach. After a successful puncture, the parenchymal tract was dilated, and covered stents were introduced. The specifications of the covered stents were 8 mm × 50 mm, 8 mm × 60 mm, 8 mm × 70 mm, and 8 mm × 80 mm. All of the diameters of the bare stents were 8 mm, and the lengths were 50-80 mm. The portal vein pressure was measured before and after shunt creation. After the insertion of TIPS, all of the participants received a diuretic treatment and a salt-limited diet.
Other names: TIPS
12 mg (body weight ≥60 kg) , 8 mg (body weight <60 kg
Tislelizumab (200mg intravenously every 3 weeks), Sintilimab (200mg intravenously every 3 weeks), Camrelizumab (200mg intravenously every 3 weeks)
Time frame: 6 months
atients occur gastrointestinal hemorrhage within 6 months after TIPS.
Time frame: 12 months
Progression was defined as progressive disease by independent radiologic review
Time frame: 24 months
OS is the length of time from the date of inclusion until death from any cause.
Time frame: 6 months
ORR, as determined based on tumor response according to RECIST 1.1, is defined as the proportion of all included patients whose best overall response (BOR) is either a complete response or partial response.
Time frame: 24 months
Safety will be evaluated according to the NCI CTCAE Version 4.03. All observations
Contact information is provided by the study sponsor or research team.
Feng Duan, MD
CONTACT
Qunfang Zhou, MD
CONTACT
Sun Yat-sen University
Other
Transjugular Intrahepatic Portosystemic Shunt Combined With Lenvatinib and PD-1 Inhibitor for Advanced Hepatocellular Carcinoma With Main Trunk Portal Vein Tumor Thrombus: a Multicenter Phase II Study
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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