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HAIC+Lenvatinib+Tislelizumab vs D-TACE+Lenvatinib+Tislelizumab for Unresectable HCC

Primary Purpose

Unresectable Hepatocellular Carcinoma

Status
Recruiting
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
D-TACE
HAIC
Lenvatinib
tislelizumab
Sponsored by
Wen Li
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Unresectable Hepatocellular Carcinoma

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with advanced unresectable hepatocellular carcinoma treated by D- TACE, or HAIC combined with Lenvatinib and Tislelizumab as initial treatment
  • Age between 18 and 75 years
  • Child-Pugh A or B liver function
  • Eastern Cooperative Oncology Group (ECOG) performance status 0-1
  • Adequate hematologic blood counts (white blood cell count >3ⅹ109/L, absolute neutrophil count >1.5ⅹ109/L, platelet count >10ⅹ109/L, hemoglobin concentration >85 g/L
  • No extrahepatic metastasis

Exclusion Criteria:

  • Severe underlying cardiac, pulmonary, or renal diseases
  • History of a second primary malignant tumor
  • Incomplete medical data
  • Loss to follow-up.

Sites / Locations

  • The Second Affiliated Hospital of Nanchang UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

HAIC+lenvatinib+tislelizumab

D-TACE+lenvatinib+tislelizumab

Arm Description

Hepatic Arterial Infusion Chemotherapy Combined With lenvatinib and tislelizumab

Transarterial chemoembolization with drug-eluting beads Combined With lenvatinib and tislelizumab

Outcomes

Primary Outcome Measures

Tumor Response
The tumor responses were evaluated by measuring the longest diameter of target lesions according to response evaluation criteria in solid tumors.(RECIST) version 1.1
Overall survival
Overall survival (OS) was measured from the initiation of transarterial therapy to the date of death or the last follow-up.
Progression-free survival
Progression-free survival (PFS) was measured from the initiation of transarterial therapy to the time of progression or recurrence or last follow-up
Cancer embolism withdraws
The degree of thrombosis withdrawal of the portal vein or hepatic vein(VP1-VP4 or I-IV).

Secondary Outcome Measures

Full Information

First Posted
October 12, 2022
Last Updated
October 14, 2022
Sponsor
Wen Li
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1. Study Identification

Unique Protocol Identification Number
NCT05582278
Brief Title
HAIC+Lenvatinib+Tislelizumab vs D-TACE+Lenvatinib+Tislelizumab for Unresectable HCC
Official Title
HAIC Combined With Lenvatinib and Tislelizumab Versus D-TACE Combined With Lenvatinib and Tislelizumab in Advanced Unresectable Hepatocellular Carcinoma
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Recruiting
Study Start Date
January 1, 2021 (Actual)
Primary Completion Date
January 1, 2024 (Anticipated)
Study Completion Date
January 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Wen Li

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Drug-eluting Bead-Transarterial chemoembolization (D-TACE) is the most widely used palliative treatment for hepatocellular carcinoma (HCC) patients. While a number of studies demonstrate poor effect of D-TACE for patients in Advanced Unresectable HCC. The investigators previous study also revealed similar results in Advanced Unresectable HCC patients treated with D-TACE. Recently, the investigators previous study demonstrated that, compared with D-TACE, hepatic arterial infusion chemotherapy (HAIC) may improve tumor response in Advanced Unresectable HCC. Thus, the investigators carried out this prospective nonrandomized control to demonstrate the superiority of HAIC-based combination therapy over D-TACE-based combination therapy.
Detailed Description
HCC is one of the most common malignant tumors with the worst prognosis. At present, except for liver transplantation, surgical resection is the most effective therapy for patients with HCC. However, many patients are found to have advanced cancer as soon as they were diagnosed and lose the opportunity of radical resection and treatments are limited.More and more clinical research failures have hit the investigators' hard, until a clinical study named IMbrave150, published in the New England Journal of Medicine in 2020. It has opened up a new era of combination therapy, breaking the pattern of only a single mode of advanced liver cancer for more than ten years, making the investigators realize that for the treatment of patients with advanced liver cancer, the single treatment effect is often very limited, and combination therapy is the future.The investigators recent research showed that HAIC Combined With Lenvatinib and Tislelizumab brings good results to patients with advanced HCC.To identify a more effective and safety way for treating potentially resectable HCC patients, this study is designed to compare the safety and efficacy between HAIC-based combination therapy and D-TACE-based combination therapy for those patients in Advanced Unresectable HCC.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Unresectable Hepatocellular Carcinoma

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
HAIC+lenvatinib+tislelizumab
Arm Type
Experimental
Arm Description
Hepatic Arterial Infusion Chemotherapy Combined With lenvatinib and tislelizumab
Arm Title
D-TACE+lenvatinib+tislelizumab
Arm Type
Experimental
Arm Description
Transarterial chemoembolization with drug-eluting beads Combined With lenvatinib and tislelizumab
Intervention Type
Drug
Intervention Name(s)
D-TACE
Other Intervention Name(s)
D-TACE+lenvatinib+tislelizumab
Intervention Description
CalliSpheres (100-300 µm) loaded with pirarubicin for transarterial chemombolization: Typically, one vial of the beads was loaded with 60 mg pirarubicin. If blushed tumors is still visible after the embolization with one vial of beads, regular microspheres (8spheres) with diameters of 100-700 μm are additionally injected.
Intervention Type
Drug
Intervention Name(s)
HAIC
Other Intervention Name(s)
HAIC+Lenvatinib+tislelizumab
Intervention Description
FOLFOX-based regimen for hepatic arterial infusion chemotherapy: oxaliplatin, 100 mg/m2 infusion for 2 hours; calcium levofolinate, 200 mg/m2 infusion for 1 hours; and 5-FU, 400 mg/m2 bolus infusion and then 2400 mg/m2 continuous infusion over 46 h.
Intervention Type
Drug
Intervention Name(s)
Lenvatinib
Other Intervention Name(s)
Targeted therapy
Intervention Description
12 mg/d for bodyweight ⩾ 60 kg or 8 mg/d for bodyweight <60 kg
Intervention Type
Drug
Intervention Name(s)
tislelizumab
Other Intervention Name(s)
PD-1 inhibitors
Intervention Description
tislelizumab 200 mg, every 3 weeks.
Primary Outcome Measure Information:
Title
Tumor Response
Description
The tumor responses were evaluated by measuring the longest diameter of target lesions according to response evaluation criteria in solid tumors.(RECIST) version 1.1
Time Frame
6-8 weeks
Title
Overall survival
Description
Overall survival (OS) was measured from the initiation of transarterial therapy to the date of death or the last follow-up.
Time Frame
24months
Title
Progression-free survival
Description
Progression-free survival (PFS) was measured from the initiation of transarterial therapy to the time of progression or recurrence or last follow-up
Time Frame
24 months
Title
Cancer embolism withdraws
Description
The degree of thrombosis withdrawal of the portal vein or hepatic vein(VP1-VP4 or I-IV).
Time Frame
6-8 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with advanced unresectable hepatocellular carcinoma treated by D- TACE, or HAIC combined with Lenvatinib and Tislelizumab as initial treatment Age between 18 and 75 years Child-Pugh A or B liver function Eastern Cooperative Oncology Group (ECOG) performance status 0-1 Adequate hematologic blood counts (white blood cell count >3ⅹ109/L, absolute neutrophil count >1.5ⅹ109/L, platelet count >10ⅹ109/L, hemoglobin concentration >85 g/L No extrahepatic metastasis Exclusion Criteria: Severe underlying cardiac, pulmonary, or renal diseases History of a second primary malignant tumor Incomplete medical data Loss to follow-up.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Wen Li, PhD
Phone
18870050597
Email
lw1042@126.com
First Name & Middle Initial & Last Name or Official Title & Degree
Lu Fang, PHD
Phone
13507911672
Email
fanglu@medmail.com.cn
Facility Information:
Facility Name
The Second Affiliated Hospital of Nanchang University
City
Nanchang
State/Province
Jiangxi
ZIP/Postal Code
330000
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Wen Li, PHD
Phone
18870050597
Email
lw1042@126.com
First Name & Middle Initial & Last Name & Degree
Lu Fang, PHD
Phone
13507911672
Email
fanglu@medmail.com.cn

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

HAIC+Lenvatinib+Tislelizumab vs D-TACE+Lenvatinib+Tislelizumab for Unresectable HCC

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