Balloon Assisted Transarterial Therapy for Hepatocellular Carcinoma

Sponsor
Chinese University of Hong Kong (Other)
Overall Status
Recruiting
CT.gov ID
NCT04780802
Collaborator
(none)
30
1
1
31.1
1

Study Details

Study Description

Brief Summary

To prove the treatment concept of the use of balloon assistance in transarterial therapy for HCC and to explore the selection criteria for clinical application of balloon assistance in transarterial therapy for HCC.

Condition or Disease Intervention/Treatment Phase
  • Procedure: The balloon catheter is placed at the various arterial feeders of the tumor
N/A

Detailed Description

Transcatheter arterial chemoembolization (TACE) has been playing an important role in the treatment algorithm for patients with multifocal or large intrahepatic lesions of hepatocellular carcinoma (HCC) not eligible for surgical resection, transplantation, or local ablative therapy. The use of balloon assisted TACE has been proposed recently and it could be one of the possible ways to improve the effectiveness of drug delivery to the target tumor and therefore leading to improved treatment outcome.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
30 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Balloon Assisted Transarterial Therapy for Hepatocellular Carcinoma: a Study on the Proof of Treatment Concept and Exploration of Selection Criteria for Clinical Application
Anticipated Study Start Date :
Jun 30, 2022
Anticipated Primary Completion Date :
Jan 31, 2024
Anticipated Study Completion Date :
Jan 31, 2025

Arms and Interventions

Arm Intervention/Treatment
Other: Ballloon catheter

Balloon-assisted transarterial therapy will be performed in the first treatment session only

Procedure: The balloon catheter is placed at the various arterial feeders of the tumor
use of a balloon catheter for providing balloon occlusion, in addition to the standard microcatheter for drug delivery, both catheters are to be placed in parallel through a single guide catheter. Only one arterial puncture wound is involved. The inflated balloon provides temporary occlusion of all arterial tumor feeders except for the one which is selectively catheterized with a microcatheter for delivery of the therapeutic agent. The therapeutic agent consists of Lipiodol mixed with a chemotherapeutic drug, it is delivered through the microcatheter under fluoroscopic control.

Outcome Measures

Primary Outcome Measures

  1. The change in hemodynamics of arterial blood supply to HCC tumors [immediately after completion of procedure]

    The change in number of feeding arteries

  2. The change in the perfusion pattern of HCC tumors [immediately after completion of procedure]

    The change in perfusion pressure.

Secondary Outcome Measures

  1. The degree of completeness of coverage of the tumor vasculature [within 30 minutes after completion of procedure]

    The degree of completeness of coverage of the tumor vasculature at the completion of the treatment as evaluated on CT scan

  2. Tumor response [3 months]

    Tumor response by CT such as complete response according to European Association for the Study of the Liver (EASL) necrosis guidelines.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Patients of age above 18 years

  2. Patients who are indicated for transarterial treatment for HCC

  3. Child-Pugh A or B cirrhosis

  4. Eastern Cooperative Oncology Group performance score 0 or 1

  5. BCLC A or B

  6. No previous treatment with liver resection, ablation, chemotherapy, radiotherapy or transarterial embolization (with or without chemotherapy),

  7. HCC diagnosed by typical enhancement patterns on cross sectional imaging or histology.

  8. No extra-hepatic involvement on non-enhanced CT thorax and triphasic contrast enhanced CT abdomen.

  9. No invasion of portal vein or hepatic vein

  10. Massive expansive tumor morphology with measurable lesion on CT (characterized by well-defined spherical or globular configuration, with or without tumor capsule or satellite lesions)

  11. Total tumor mass < 50% liver volume

  12. Size of any individual tumor <= 7cm in largest dimension

  13. Serum creatinine < 130 umol/L or Creatinine clearance > 55 ml/min.

Exclusion Criteria:
  1. Concurrent ischemic heart disease or heart failure

  2. History of asthma, chronic obstructive airway disease or respiratory decompensation.

  3. History of acute tumor rupture presenting with hemo-peritoneum

  4. Biliary obstruction not amenable to percutaneous or endoscopic drainage

  5. Child-Pugh C cirrhosis

  6. History of hepatic encephalopathy

  7. Intractable ascites not controllable by medical therapy

  8. History of variceal bleeding within last 3 months

  9. Serum total bilirubin level > 50 umol/L

  10. Serum albumin level < 26 g/L

  11. INR > 1.3

  12. Infiltrative tumor morphology (characterized by ill- defined tumor margin and amorphous configuration) or diffuse tumor morphology (characterized by large number of small nodules)

  13. Arterio-portal venous shunt affecting >1 hepatic segment on CT

  14. Arterial-hepatic venous shunt with hepatic vein opacified in arterial phase on CT

Contacts and Locations

Locations

Site City State Country Postal Code
1 Department of Imaging and Interventional Radiology, Prince of Wales Hospital, The Chinese University of Hong Kong Hong Kong Hong Kong

Sponsors and Collaborators

  • Chinese University of Hong Kong

Investigators

  • Principal Investigator: Simon Yu, Professor, DIIR, CUHK, Hong Kong

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Simon Yu, Professor, Chinese University of Hong Kong
ClinicalTrials.gov Identifier:
NCT04780802
Other Study ID Numbers:
  • VIR-20-13
First Posted:
Mar 4, 2021
Last Update Posted:
Mar 11, 2022
Last Verified:
Mar 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 11, 2022