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Not yet recruitingNCT04319484LLTHVVUpdated Mar 24, 2020

Lenvatinib Following Liver Transplantation in Patients of Hepatocellular Carcinoma With Portal Vein Tumor Thrombus

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

From the registry’s dates

  • Primary completion was expected by Jan 2025, 1 year 9 months ago, but the record still lists the study as not yet recruiting.
Phase
Phase 2/3
Study type
Interventional
Enrollment
108
Allocation
Randomized
Ages
1 Year to 75 Years
Sex
All
01

Study summary

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.

Read the detailed description

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).

02

Conditions studied

  • Hepatocellular Carcinoma
  • Portal Vein Tumor Thrombus
  • Liver Transplantation

Keywords

  • Liver Transplantation
  • Hepatocellular Carcinoma
  • Portal Vein Tumor Thrombus
  • Lenvatinib
03

In context

Carcinoma

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 →

Lead sponsor

RenJi Hospital is the lead sponsor of 535 studies on the registry; 244 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
1 Year to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Patients who underwent liver transplantation were preoperatively imaging diagnosed as hepatocellular carcinoma with portal vein tumor thrombus.
  2. Male or female patients aged 18 to 75.
  3. ECOG physical condition was 0-2 points.
  4. Child-Pugh A grade of liver function.
  5. Targeted therapy is acceptable within 1-2 months after liver transplantation.
  6. Immunosuppressive regimen consists of calcineurin inhibitor, mycophenolate mofetil and sirolimus.
  7. No history of surgical resection of liver tumors and targeted drug therapy before liver transplantation.
  8. Good liver, kidney and bone marrow function: serum albumin > 28g/L, total bilirubin ≤ 3 mg/dL (51.3 umol/l), ALT and AST ≤ 5 times the upper limit of normal range; serum creatinine ≤ 1.5 times the upper limit of normal range; hemoglobin > 90 g/L, neutrophil count (ANC) > 1.5 * 10 \^ 9/L, platelet count > 60 * 10 \^ 9/L; PT-INR \< 2.3, or PT within 6 seconds over normal upper limit.
  9. For fertile female patients, the serum/urine pregnancy test should be negative within 7 days before treatment.
  10. All male and female participants must take reliable contraceptive measures during the trial and within four weeks after the end of the trial.
  11. The participants have the capability of oral medication.
  12. The participants must sign the consent form.

Exclusion criteria

Exclusion Criteria:

  1. Hepatocellular carcinoma with invasion of hepatic vein and inferior vena cava
  2. Life expectancy is less than 3 months
  3. The recurrence and metastasis of hepatocellular carcinoma are highly suspected.
  4. Patients are with other malignant tumors simultaneously.
  5. Patients are anaphylaxis to the inactive ingredients of lenvatinib or drugs.
  6. Pregnant or lactating women (Female participants need pregnancy test within 7 days before treatment).
  7. Preoperative history of severe cardiovascular disease: congestive heart failure > NYHA grade 2; active coronary heart disease (myocardial infarction occurred within 6 months before entry into the study); severe arrhythmia requiring antiarrhythmic treatment (allowable use of beta-blockers or digoxin); uncontrolled hypertension.
  8. History of HIV infection.
  9. Severe clinical active infections (> NCI-CTCAE version 3.0).
  10. Epilepsy patients requires medication (e.g. steroids or antiepileptic drugs).
  11. Patients with kidney diseases requires renal dialysis.
  12. Drug abuse, medical symptoms, mental illness or social status that may interfere with participants'participation in research or evaluation of research results.
  13. Patients who could not swallow oral drugs, such as those with severe upper gastrointestinal obstruction and need gastric tube feeding.
  14. Other anti-angiogenesis therapies, surgery, TACE, local therapy and systemic chemotherapy were given before the treatment after liver transplantation.
05

Study design

Phase
Phase 2 / Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
108 participants (estimated)

Study arms

  • Experimental
    lenvatinib

    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

  • Placebo comparator
    Placebo

    The placebo pills are made identical to the investigating lenvatinib in appearance

    Drug: Placebo

Interventions

  • Druglenvatinib

    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

  • DrugPlacebo

    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

06

What researchers measure

Primary outcomes

  1. 3 years recurrence-free survival rate

    Tumor-free survival in 3 years

    Time frame: 3 years

Secondary outcomes

  1. 1 year recurrence-free survival rate

    Tumor-free survival in 1 years

    Time frame: 1 years

  2. 1 year overall survival rate

    Overall survival refers to the time from treatment to death for any reason.

    Time frame: 1 year

  3. 3 years overall survival rate

    Overall survival refers to the time from treatment to death for any reason.

    Time frame: 3 years

  4. 5 years overall survival rate

    Overall survival refers to the time from treatment to death for any reason.

    Time frame: 5 years

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 24, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04319484
Lead sponsor
RenJi Hospital
Responsible party
Sponsor
First posted
Mar 24, 2020
Start date
May 2, 2020 (estimated)
Primary completion
Jan 1, 2025 (estimated)
Completion
Dec 1, 2025 (estimated)
Last update
Mar 24, 2020

Study contacts

qiang xia, doctor
Contact
xiaqiang1966@126.com
+8613661889035
qiang xia, doctor
study chair · RenJi Hospital

Oversight

Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

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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