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Clinical Trials/NCT05625893
NCT05625893
Recruiting
Phase 2

Proton Beam Radiotherapy Followed by Tecentriq and Avastin for Primary Liver Cancer With Vp2-4 Portal Vein Invasion: PORTAL Study

Samsung Medical Center1 site in 1 country63 target enrollmentJanuary 15, 2023

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Hepatocellular Carcinoma
Sponsor
Samsung Medical Center
Enrollment
63
Locations
1
Primary Endpoint
Incidence of adverse event assessed according to the Common Terminology Criteria for Adverse Events (CTCAE version 5.0)
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

This study is investigator initiated, single-institution, prospective, phase 2 open-label study to determine the efficacy and safety of combination therapy of atezolizumab/bevacizumab and proton beam therapy to portal vein tumor thrombosis with or without main primary tumor in patients with stage 3 or higher hepatocellular carcinoma (HCC) with Vp2-4 portal vein invasion who had not undergone systemic therapy for HCC. The primary endpoint of this study is progression-free survival and secondary endpoints are overall survival (OS), time to progression (TTP), objective response rate, disease control rate (DCR), and time to local disease progression (LTP).

Registry
clinicaltrials.gov
Start Date
January 15, 2023
End Date
November 2026
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Jeong Il Yu

Assistant Professor

Samsung Medical Center

Eligibility Criteria

Inclusion Criteria

  • Patients with HCC meeting all of following criteria;
  • Histologically or radiologically confirmed hepatocellular carcinoma based on the guidelines of the Korean Liver Cancer Association-National Cancer Center 2022
  • Vp2-4 portal vein tumor thrombosis diagnosed by dynamic enhanced computed tomography (CT) or maganetic resonance images (MRI) with below finding 1) an intraluminal filling defect adjacent to the primary tumor in Vp2-4 portal vein 2) an enhancement of the filling defect on arterial phase and a washout on portal/delayed phases.
  • Signed written informed consent
  • at least one or more measurable intrahepatic viable HCC lesions
  • Child-Pugh class A within 2 weeks from screening for study registration
  • Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0-1 within 2 weeks from screening for study registration
  • Life expectancy of at least 16 weeks
  • adequate bone marrow and liver function within 2 weeks from screening for study registration
  • Hemoglobin ≥ 9.0 g/dL

Exclusion Criteria

  • Patients with HCC meeting all of following criteria;
  • previous history of systemic treatment for HCC (If systemic treatment for HCC has been performed at least once, it will not be enrolled in this study.) However, registration is permitted if the previous systemic treatment is for adjuvant purposes or treatment for other cancers. Also allowed if previous HCC treatment is local treatment. However, cases with a history of previous upper abdominal radiotherapy (including proton therapy and heavy particle therapy) are excluded.
  • any type of anticancer agent (including investigational) within 2 weeks before enrollment
  • Having active brain metastasis or leptomeningeal metastasis need surgery or steroid therapy
  • Moderate to severe or intractable ascites
  • A history or presence of hepatic encephalopathy
  • Presence of active bacterial infection
  • Untreated active chronic hepatitis B or active hepatitis C
  • History of portal hypertension with bleeding within the past 6 months
  • Prior liver transplant

Outcomes

Primary Outcomes

Incidence of adverse event assessed according to the Common Terminology Criteria for Adverse Events (CTCAE version 5.0)

Time Frame: From date of atezolizumab and bevacizumab initiatton until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 18 months

Progression-free survival rate

Time Frame: At 9 month

Secondary Outcomes

  • Objective response rate(At 3 month)
  • Disease Control rate(At 3 month)
  • Local tumor progression rate(At 12 month)
  • Overall survival rate(At 12 month)
  • Time-to-progression(At 9 months)

Study Sites (1)

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