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Role of DEB-TACE Versus c-TACE in Treatment of HCC

Primary Purpose

Hepatocellular Carcinoma

Status
Active
Phase
Early Phase 1
Locations
Egypt
Study Type
Interventional
Intervention
Doxorubicin-Eluting Beads
Sponsored by
Sohag University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hepatocellular Carcinoma

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • - Child-Pugh A or B cirrhosis.
  • ECOG performance status (PS) Grade 2 or below.
  • BCLC stage B or C.
  • No serious concurrent medical illness.
  • Radiologically or histologically proven HCC (an alpha-fetoprotein level > 500 ug/ml in the presence of radiological findings suggestive of HCC in a patient with chronic HBV or HCV infection is considered eligible).
  • Unresectable and locally advanced disease without extra-hepatic disease.
  • Nodular tumor morphology with measurable lesion on CT with less than 50% involvement of liver by HCC.
  • Size of largest tumor is less than or equal to 15cm in largest dimension.
  • Number of main tumor is less than or equal to 5, excluding associated small satellite lesions.
  • Patent main portal vein.

Exclusion Criteria:

  • - Child-Pugh C cirrhosis (evidence of poor liver function).
  • History of significant concurrent medical illness such as ischemic heart disease or heart failure.
  • Serum creatinine level > 2 mg/dL.
  • Presence of extrahepatic metastasis.
  • Predominantly infiltrative lesion.
  • Diffuse tumor morphology with extensive lesions involving both lobes.
  • Hepatic artery thrombosis.
  • Thrombosis of the main portal vein.
  • Tumor invasion of portal branch of contralateral lobe.

Sites / Locations

  • Sohag University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Drug Eluting Bead Transarterial Chemoembolization

conventional Transarterial Chemoembolization

Arm Description

Drug Eluting Bead Transarterial Chemoembolization

conventional Transarterial Chemoembolization

Outcomes

Primary Outcome Measures

Tumor size
Triphasic CT scan of the liver measures the maximum diameter of tumor according to modified RECIST (mRecist) criteria.

Secondary Outcome Measures

Serum Alpha-fetoprotein level ng/ml.
Laboratory test of Serum alpha-fetoprotein level (AFP) ng/ml.

Full Information

First Posted
October 13, 2021
Last Updated
April 10, 2023
Sponsor
Sohag University
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1. Study Identification

Unique Protocol Identification Number
NCT05093920
Brief Title
Role of DEB-TACE Versus c-TACE in Treatment of HCC
Official Title
Role of Drug Eluting Bead Transarterial Chemoebolization Versus Conventional Transarterial Chemoembolization in Treatment of Hepatocellular Carcinoma
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
January 1, 2022 (Actual)
Primary Completion Date
December 1, 2023 (Anticipated)
Study Completion Date
January 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Sohag University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Hepatocellular carcinoma (HCC) is listed as the sixth most common cancer worldwide and the third most frequent cause of cancer-related mortality. The majority of HCC cases occurs stem from chronic liver disease and cirrhosis. Hepatocellular carcinoma accounts for approximately 70% to 90% of all primary liver cancers. Trans-arterial Chemoembolization is the most widely utilized and is considered the first-line treatment recommended for patients staged as intermediate HCC (Barcelona Clinic Liver Cancer stage B). If applied correctly, TACE can produce survival benefits without adversely affecting hepatic functional reserve. Two TACE techniques have been used since 2004, conventional TACE (c-TACE) and TACE with drug-eluting beads (DEB-TACE). Conventional TACE was evidenced first to treat intermediate stage HCC patients.
Detailed Description
Hepatocellular carcinoma (HCC) is listed as the sixth most common cancer worldwide and the third most frequent cause of cancer-related mortality. The majority of HCC cases occurs stem from chronic liver disease and cirrhosis. Hepatocellular carcinoma accounts for approximately 70% to 90% of all primary liver cancers. HCC patients have been suffering from poor prognosis with 5-year survival being roughly 10% to 15% for decades despite the progress in screening, diagnosis, and treatment, which is mainly resulted from that most patients are already in the moderate or advanced stage at diagnosis, whom can only receive palliative treatments. At the level of the individual patient, concomitant cirrhosis and the number, size, and location of hepatocellular tumors will affect the treatment approach. In addition, multiple disease-related factors need to be taken into account, such as the presence of vascular involvement or extra-hepatic disease, when deciding on the best treatment options for these patients. Consequently, a multidisciplinary approach involving several physicians with different specialties (e.g., diagnostic and interventional radiologists, surgical oncologists, hepatologists, and medical oncologists) is necessary to determine the best approach to treatment and maximize potential outcomes for patients with HCC. The liver has a dual vascular supply via the hepatic artery and the portal vein. The rationale of the trans-arterial embolotherapies is explained by the fact that liver malignancies are predominantly supplied by the hepatic artery, which allows delivering the chemotherapy directly to the tumor-feeding artery while sparing the healthy hepatic tissue mainly supplied by the portal vein. Loco regional treatments are a set of therapeutic approaches that directly target tumors in the liver. Among the loco regional modalities, trans-arterial chemoembolization (TACE) involves the local delivery of chemotherapy to the tumor and is generally recommended for patients with liver-limited disease. Several randomized trials have been conducted to examine the efficacy and safety of TACE. According to the Barcelona Clinic Liver Cancer (BCLC) staging system, TACE is the first-line treatment for patients with intermediate stage HCC, including those with large or multinodular HCC, well-preserved liver function, and no cancer-related symptoms or evidence of vascular invasion or extrahepatic spread. Recent advances allow TACE treatment of both early stage patients (i.e. those with a solitary nodule or up to 3 nodules under 3 cm) and some advanced stage patients. Trans-arterial Chemoembolization is the most widely utilized and is considered the first-line treatment recommended for patients staged as intermediate HCC (Barcelona Clinic Liver Cancer stage B). If applied correctly, TACE can produce survival benefits without adversely affecting hepatic functional reserve. Two TACE techniques have been used since 2004, conventional TACE (c-TACE) and TACE with drug-eluting beads (DEB-TACE). Conventional TACE was evidenced first to treat intermediate stage HCC patients. It combines the trans-catheter delivery of chemotherapy using Lipiodol-based emulsion plus an embolizing agent to achieve strong cytotoxic and ischemic effects. Drug-eluting beads (DEB) were developed in order to slowly release chemotherapeutic agents, and to increase ischemia intensity and duration. The introduction of TACE with drug eluting beads (DEB-TACE) was primarily developed to enhance the delivery of the chemotherapeutic agent while minimizing systemic toxicity and to provide a standardized embolizing effect. DEBs are embolic microspheres loaded with a chemotherapeutic agent (mostly doxorubicin) with the ability of slow drug release, which should ensure high local and low systemic drug concentrations. Indeed, systemic levels of doxorubicin were significantly lower in patients receiving DEB-TACE compared to patients receiving c-TACE with Lipiodol. DEB-TACE was introduced 10 years ago with the aim to improve the overall c-TACE outcomes and to diminish the side effects of the procedure. It is based on the use of microspheres that exploit ionic bonds and are able to actively sequester and then slowly release the cytotoxic drug inside the target lesion. Moreover, the use of particles allows a deeper distal embolization of small vessels, ensuring a permanent highly selective occlusion of the tumor-feeding arteries. DEB-TACE has several advantages over c-TACE, such as the delivery of higher concentrations of chemotherapeutic agents directly to tumors, lower rates of systemic complications, greater efficacy in advanced stage or large tumors, and better standardization of the procedure itself.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatocellular Carcinoma

7. Study Design

Primary Purpose
Treatment
Study Phase
Early Phase 1
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
30 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Drug Eluting Bead Transarterial Chemoembolization
Arm Type
Active Comparator
Arm Description
Drug Eluting Bead Transarterial Chemoembolization
Arm Title
conventional Transarterial Chemoembolization
Arm Type
Active Comparator
Arm Description
conventional Transarterial Chemoembolization
Intervention Type
Drug
Intervention Name(s)
Doxorubicin-Eluting Beads
Other Intervention Name(s)
Lipidol-Doxorubicin emulsion
Intervention Description
The patients will be categorized in two randomized groups; c-TACE group (A) and DEB-TACE group (B). After patient counseling and obtaining a written consent to participate in the study, both groups will be subjected to the interventional procedure according to patient group; Group A; Lipidol-Doxorubicin emulsion material followed by gel foam embolic material will be injected through the catheter directly into tumor feeding vessels through transarterial catheter. Group B; Doxorubicin-Eluting Beads will be injected through the catheter directly into tumor feeding vessels through transarterial catheter.
Primary Outcome Measure Information:
Title
Tumor size
Description
Triphasic CT scan of the liver measures the maximum diameter of tumor according to modified RECIST (mRecist) criteria.
Time Frame
four-six weeks after treatment
Secondary Outcome Measure Information:
Title
Serum Alpha-fetoprotein level ng/ml.
Description
Laboratory test of Serum alpha-fetoprotein level (AFP) ng/ml.
Time Frame
four-six weeks after treatment

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: - Child-Pugh A or B cirrhosis. ECOG performance status (PS) Grade 2 or below. BCLC stage B or C. No serious concurrent medical illness. Radiologically or histologically proven HCC (an alpha-fetoprotein level > 500 ug/ml in the presence of radiological findings suggestive of HCC in a patient with chronic HBV or HCV infection is considered eligible). Unresectable and locally advanced disease without extra-hepatic disease. Nodular tumor morphology with measurable lesion on CT with less than 50% involvement of liver by HCC. Size of largest tumor is less than or equal to 15cm in largest dimension. Number of main tumor is less than or equal to 5, excluding associated small satellite lesions. Patent main portal vein. Exclusion Criteria: - Child-Pugh C cirrhosis (evidence of poor liver function). History of significant concurrent medical illness such as ischemic heart disease or heart failure. Serum creatinine level > 2 mg/dL. Presence of extrahepatic metastasis. Predominantly infiltrative lesion. Diffuse tumor morphology with extensive lesions involving both lobes. Hepatic artery thrombosis. Thrombosis of the main portal vein. Tumor invasion of portal branch of contralateral lobe.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ahmed E Mohamed, Master
Organizational Affiliation
Sohag University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Mohamed Z Ali, MD
Organizational Affiliation
Sohag University
Official's Role
Study Chair
Facility Information:
Facility Name
Sohag University Hospital
City
Sohag
ZIP/Postal Code
88525
Country
Egypt

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
33919658
Citation
Cho SM, Chu HH, Kim JW, Kim JH, Gwon DI. Initial Transarterial Chemoembolization (TACE) Using HepaSpheres 20-40 microm and Subsequent Lipiodol TACE in Patients with Hepatocellular Carcinoma > 5 cm. Life (Basel). 2021 Apr 18;11(4):358. doi: 10.3390/life11040358.
Results Reference
background
PubMed Identifier
31234476
Citation
Gholam PM, Iyer R, Johnson MS. Multidisciplinary Management of Patients with Unresectable Hepatocellular Carcinoma: A Critical Appraisal of Current Evidence. Cancers (Basel). 2019 Jun 22;11(6):873. doi: 10.3390/cancers11060873.
Results Reference
background
PubMed Identifier
31124925
Citation
Li H, Wu F, Duan M, Zhang G. Drug-eluting bead transarterial chemoembolization (TACE) vs conventional TACE in treating hepatocellular carcinoma patients with multiple conventional TACE treatments history: A comparison of efficacy and safety. Medicine (Baltimore). 2019 May;98(21):e15314. doi: 10.1097/MD.0000000000015314.
Results Reference
background
PubMed Identifier
29987957
Citation
Melchiorre F, Patella F, Pescatori L, Pesapane F, Fumarola E, Biondetti P, Brambillasca P, Monaco C, Ierardi AM, Franceschelli G, Carrafiello G. DEB-TACE: a standard review. Future Oncol. 2018 Dec;14(28):2969-2984. doi: 10.2217/fon-2018-0136. Epub 2018 Jul 10.
Results Reference
background

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Role of DEB-TACE Versus c-TACE in Treatment of HCC

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