Actively Recruiting

Age: 18Years - 75Years
All Genders
NCT06333561

HAIC Combined With Lenvatinib and PD-1 Inhibitor in Infiltrative Hepatocellular Carcinoma

Led by Sun Yat-sen University · Updated on 2025-02-06

300

Participants Needed

1

Research Sites

260 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Hepatic arterial infusion chemotherapy (HAIC) plus lenvatinib and programmed cell death protein-1 (PD-1) inhibitor have shown promising results for advanced hepatocellular carcinoma (HCC). However, the evidence for infiltrative is limited. In this study, we aimed to describe the efficacy and safety of lenvatinib and PD-1 inhibitor with HAIC plus lenvatinib for infiltrative HCC.

CONDITIONS

Official Title

HAIC Combined With Lenvatinib and PD-1 Inhibitor in Infiltrative Hepatocellular Carcinoma

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Primary infiltrative hepatocellular carcinoma confirmed by MRI or CT imaging
  • Child-Pugh class A or B liver function
  • Eastern Cooperative Oncology Group performance status of 0 or 1
  • Lenvatinib used as initial treatment
  • Patients receiving HAIC plus lenvatinib and PD-1 inhibitor, or lenvatinib alone
  • No history of other cancers
  • No tumor thrombus in the atrium or vena cava
Not Eligible

You will not qualify if you...

  • Hepatocellular carcinoma with tumor capsule
  • Younger than 18 years or older than 75 years
  • Transarterial chemoembolization (TACE) as initial treatment
  • Use of sorafenib or other systemic therapy with or without PD-1 inhibitor after HAIC
  • Incomplete tumor imaging data
  • Lost to follow-up within three months after treatment

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Chinese PLA General hospital

Beijing, Beijing Municipality, China, 100853

Actively Recruiting

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Research Team

Q

Qunfang Zhou, MD

CONTACT

F

Feng Duan, MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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