Actively Recruiting

Age: 18Years +
All Genders
NCT06669377

TACE Combined With ICIs Plus MTT After 125I Irradiation Stent Placement in HCC With Main PVTT.

Led by Zhongda Hospital · Updated on 2024-11-01

444

Participants Needed

1

Research Sites

65 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Hepatocellular carcinoma (HCC) patients with Vp4 \[main trunk\] portal vein tumor thrombosis (PVTT) face a significantly poor prognosis, and current treatment options provide limited benefits. We aimed to assess the safety and efficacy of transcatheter arterial chemoembolization (TACE) combined with immune checkpoint inhibitors (ICIs) plus molecular targeted therapy (MTT) after irradiation stent placement (ISP) as first line treatment for HCC patients with Vp4 PVTT.

CONDITIONS

Official Title

TACE Combined With ICIs Plus MTT After 125I Irradiation Stent Placement in HCC With Main PVTT.

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Diagnosis of hepatocellular carcinoma confirmed by tissue or clinical features
  • Portal vein tumor thrombosis extending to the main portal vein (Vp4) confirmed by histology or imaging
  • At least one measurable liver lesion as per RECIST version 1.1
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or 2
  • Receiving first-line treatment with either ICIs plus molecular targeted therapy or with irradiation stent placement plus TACE within eight weeks
Not Eligible

You will not qualify if you...

  • Presence of cancer spread outside the liver (extrahepatic metastases)
  • History of or current other cancers
  • Prior systemic or local treatments including surgery, radiation, hepatic arterial embolization, TACE, hepatic arterial infusion, radiofrequency ablation, ethanol injection, or cryoablation within 3 months before stent placement
  • Severe liver dysfunction (Child-Pugh grade C), ascites score of 3, or overt hepatic encephalopathy
  • Missing important outcome data or baseline information needed for analysis

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

Zhongda Hospital

Nanjing, Jiangsu, China, 210009

Actively Recruiting

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Research Team

J

Jian Lu, M.D.

CONTACT

G

Gaojun Teng, M.D.

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

0

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