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Clinical Trials/NCT01850368
NCT01850368
Completed
Phase 2

Multicenter Phase II Study of Stereotactic Ablative Radiotherapy for Hepatocellular Carcinoma With Major Portal Vein Invasion

Korea Cancer Center Hospital8 sites in 1 country35 target enrollmentOctober 2012

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Hepatocellular Carcinoma
Sponsor
Korea Cancer Center Hospital
Enrollment
35
Locations
8
Primary Endpoint
Tumor stabilization rate
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

Recently, several studies reported promising outcomes of patients after external beam radiotherapy (EBRT) for hepatocellular carcinoma (HCC) with portal vein tumor thrombosis. However, conventional EBRT is composed of many fractions (20-35 fractions). On the other hand, stereotactic ablative radiotherapy is a newly emerging treatment method to deliver a high dose of radiation to the target using a few fractions with a high precision within body. SABR increases radiation biologic effect for tumor, makes patients more comfortable due to reduction of the number of hospital visit, and enables patients to receive another treatment more quickly. This study will evaluate SABR effect with 40 Gy in 4 fractions for HCC with major portal vein tumor thrombosis.

Registry
clinicaltrials.gov
Start Date
October 2012
End Date
July 2017
Last Updated
6 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Korea Cancer Center Hospital
Responsible Party
Principal Investigator
Principal Investigator

Mi-Sook Kim

Doctor

Korea Cancer Center Hospital

Eligibility Criteria

Inclusion Criteria

  • Male or female patients ≥ 20 years of age
  • Initially diagnosed or recurrent hepatocellular carcinoma (HCC)
  • Eastern Cooperative Oncology Group performance status 0 or 1
  • HCC with major portal vein tumor thrombosis (tumor thrombosis in the main portal vein or 1st branch of portal vein)
  • Cirrhotic status of Child Pugh class A or B7
  • Patients can have extra-hepatic disease; provided the hepatic disease is the highest burden, the extra-hepatic disease is low burden and potentially treatable with radiotherapy, chemotherapy and target agent etc; patient survival is expected to be at least 6 months.
  • Patient or guardian must be able to provide verbal and written informed consent

Exclusion Criteria

  • Prior trans-arterial chemo-embolization ≥4 after diagnosis of major portal vein tumor thrombosis
  • Severe complication caused by liver cirrhosis eg. variceal bleeding, poorly controlled ascites, hepatic encephalopathy)
  • Uncontrolled inter-current illness except liver cirrhosis

Outcomes

Primary Outcomes

Tumor stabilization rate

Time Frame: 2 months

Tumor stabilization rate was based on the combined number of patients with complete response(CR), partial response(PR), and stable disease(SD) by modified Response Evaluation Criteria in Solid Tumors (mRECIST) criteria.

Secondary Outcomes

  • Overall survival(6 months, 1 year and 2 year)
  • Tumor progression free survival(6 months, 1 year and 2 year)
  • Treatment related toxicity(1 year)

Study Sites (8)

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