A Phase 2/3 interventional study of lenvatinib and Placebo in Hepatocellular Carcinoma, Portal Vein Tumor Thrombus and Liver Transplantation, sponsored by RenJi Hospital. Not yet recruiting. Open to participants aged 1 Year to 75 Years. Per ClinicalTrials.gov, last updated 2020-03-24.
Sponsored by RenJi Hospital · Phase 2/3, Interventional, and Treatment
The aim of this study is to observe the efficacy and safety of lenvatinib in preventing recurrence of hepatocellular carcinoma patients with portal vein tumor thrombus after liver transplantation.
The research is an open, randomized, single-center study. Patients of hepatocellular carcinoma with portal vein cancer thrombus who underwent liver transplantation are included according to the criteria of admission. After operation, the regimen of calcineurin inhibitors, mycophenolate mofetil, sirolimus or everolimus with glucocorticoids removed at an early stage are used. Patients enrolled in the study were randomly allocated in the lenvatinib group (54 patients) and the control group (54 patients) after stable condition. Patients in the control group are given supportive treatment and regular follow-up. Patients in the lenvatinib group are given lenvatinib within 1-2 months after operation (dose: body weight \< 60 kg: 8 mg/day, body weight ≥ 60 kg 12 mg/day). The baseline data of patients are collected before allocation. Serum and imaging examination are checked regularly every month to monitor the recurrence of hepatocellular carcinoma and the side effects of lenvatinib. The efficacy and safety of lenvatinib in patients of hepatocellular carcinoma with portal vein tumor thrombus are observed, and the clinicopathological factors affecting the efficacy of lenvatinib are analyzed. When side effects of lenvatinib occur, the dosage can be reduced according to the patients' condition until discontinuation. When tumor recurrence occurs, a multidisciplinary team will draw up specific treatment plans according to the patients' condition, including surgical resection, interventional therapy, radiofrequency therapy, radiotherapy and targeted therapy (Patients in the control group can add lenvatinib, and patients in the lenvatinib group can decide whether to continue using it according to the patients' condition).
6,741 studies on the registry are indexed under Carcinoma; 1,163 are open to participants now.
This study's planned enrollment of 108 is above the median of 45 across 5,174 interventional studies indexed under Carcinoma.
Browse Carcinoma studies →RenJi Hospital is the lead sponsor of 535 studies on the registry; 244 are open to participants now.
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Exclusion Criteria:
Patients in the lenvatinib group are given lenvatinib within 1-2 months after operation (dose: body weight \< 60 kg: 8 mg/day, body weight ≥ 60 kg 12 mg/day).
Drug: lenvatinib
The placebo pills are made identical to the investigating lenvatinib in appearance
Drug: Placebo
1-2 months after liver transplantation, participants are given lenvatinib with an initial dose of 8 mg (body weight \< 60 kg) or 12 mg orally once a day. The initial dose was 8 mg (body weight \< 60 kg) or 12 mg orally once a day.
Also known as: experiment
1-2 months after liver transplantation, participants are given Placebo with an initial dose of 8 mg (body weight \< 60 kg) or 12 mg orally once a day. The initial dose was 8 mg (body weight \< 60 kg) or 12 mg orally once a day.
Also known as: Control
3 years recurrence-free survival rate
Tumor-free survival in 3 years
Time frame: 3 years
1 year recurrence-free survival rate
Tumor-free survival in 1 years
Time frame: 1 years
1 year overall survival rate
Overall survival refers to the time from treatment to death for any reason.
Time frame: 1 year
3 years overall survival rate
Overall survival refers to the time from treatment to death for any reason.
Time frame: 3 years
5 years overall survival rate
Overall survival refers to the time from treatment to death for any reason.
Time frame: 5 years
No study locations are listed for this record.
Plan to share: No
No publications or documents are linked to this record.
This study is not yet recruiting, as verified in Mar 2020. You cannot join it, but the record below documents what was studied.
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