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TACE and Adefovir Compared With Transarterial Chemoembolization (TACE) Alone for Hepatitis B Virus (HBV)-Related Unresectable Hepatocellular Carcinoma (HCC) (TACE)

Primary Purpose

Hepatitis B Virus, Hepatocellular Carcinoma

Status
Unknown status
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
adefovir
TACE
Sponsored by
Tongji University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hepatitis B Virus focused on measuring HBV-related unresectable HCC, TACE, adefovir, recurrence rate

Eligibility Criteria

20 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • age:20-75 years old
  • with a clinical diagnosis of primary liver cancer, with HBsAg positive,without any therapy for tumor
  • single lesion with a diameter >6.5 cm,or multiple lesions locating within half liver or adjacent three lobe
  • estimated liver remnant volume ≤40%
  • with a liver function of Child-Pugh class A,and ALT≤80IU/l.

Exclusion Criteria:

  • reject to attend
  • portal vein trunk has been compressed by tumor
  • diffuse type cancer or with extensive cancer thrombus in main branches of PV,HV,IVC or bile duct
  • with extrahepatic metastasis
  • with obvious portal hypertension (with moderate to severe varix in esophagus and/or gastric fundus, enlarged spleen,WBC<4×109/L, PLT<80×109/L)
  • with diabetes
  • allergy to iodine

Sites / Locations

  • The Fourth Affiliated Hospital of Haerbin Medical UniversityRecruiting
  • Shanghai 10th Hospital of Tongji UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

TACE

TACE+adefovir

Arm Description

An emulsion that consisted of 50 mg of cisplatin and 10 mL of lipiodol at a volume ratio of 1:1 was injected into the blood supply artery of the tumor under fluoroscopic guidance. The injection could be slowed or discontinued if retrograde flow occurred. Embolization was subsequently performed with granules of gelatin sponge particles.

patients received adefovir, at a dose of 10 mg daily after TACE treatment, for 48 weeks

Outcomes

Primary Outcome Measures

the progression free survival (PFS)

Secondary Outcome Measures

the rate of overall survival

Full Information

First Posted
August 14, 2009
Last Updated
August 14, 2009
Sponsor
Tongji University
Collaborators
Interventional Radiology Research Group, Shanghai Radiology Society
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1. Study Identification

Unique Protocol Identification Number
NCT00960518
Brief Title
TACE and Adefovir Compared With Transarterial Chemoembolization (TACE) Alone for Hepatitis B Virus (HBV)-Related Unresectable Hepatocellular Carcinoma (HCC)
Acronym
TACE
Official Title
Combination Therapy With TACE and Adefovir Compared With TACE Alone for HBV-related Unresectable Hepatocellular Carcinoma
Study Type
Interventional

2. Study Status

Record Verification Date
August 2009
Overall Recruitment Status
Unknown status
Study Start Date
August 2009 (undefined)
Primary Completion Date
August 2012 (Anticipated)
Study Completion Date
August 2015 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
Tongji University
Collaborators
Interventional Radiology Research Group, Shanghai Radiology Society

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Hepatocellular carcinoma (HCC) is one of the most prevalent malignancies in China, and approximately 90% of the patients with HCC are also infected with hepatitis B virus (HBV). For patients with unresectable disease, the goal of palliative treatment is to control symptoms and prolong survival. Transarterial chemoembolization (TACE) using iodized oil and chemotherapeutic agents combines the effect of targeted chemotherapy with that of ischemic necrosis induced by arterial embolization. It can be administered repeatedly and can prolong survival in patients with unresectable hypervascular HCC. The long-term prognosis, however, remains guarded because of frequent development of locoregional tumor recurrence, which, together with concomitant hepatic decompensation, is the main cause of death. Adefovir works by blocking reverse transcriptase, an enzyme that is crucial for the hepatitis B virus (HBV) to reproduce in the body. Based on these results, the investigators conducted a randomized controlled trial to test the hypothesis that adefovir treatment would reduce or postpone the recurrence rate and improve the overall survival rate in patients after TACE treatment of HBV-related unresectable HCC.
Detailed Description
Hepatocellular carcinoma (HCC) is one of the most prevalent malignancies in China, and approximately 90% of the patients with HCC are also infected with hepatitis B virus (HBV). Until now, no standard therapy has been established for treatment of hepatocellular carcinoma. For patients with unresectable disease, the goal of palliative treatment is to control symptoms and prolong survival. Transarterial chemoembolization (TACE) using iodized oil and chemotherapeutic agents combines the effect of targeted chemotherapy with that of ischemic necrosis induced by arterial embolization. It can be administered repeatedly and can prolong survival in patients with unresectable hypervascular HCC. The long-term prognosis, however, remains guarded because of frequent development of locoregional tumor recurrence, which, together with concomitant hepatic decompensation, is the main cause of death. Recurrence in the liver remnant may originate from metastasis from the primary tumor or multicentric new primaries in a cirrhotic liver. Adefovir works by blocking reverse transcriptase, an enzyme that is crucial for the hepatitis B virus (HBV) to reproduce in the body. It is approved for the treatment of chronic hepatitis B in adults with evidence of active viral replication and either evidence of persistent elevations in serum aminotransferases (primarily ALT) or histologically active disease. The main benefit of adefovir over lamivudine (the first NRTI approved for the treatment of hepatitis B) is that it takes a much longer period of time before the virus develops resistance to it. Adefovir dipivoxil contains two pivaloyloxymethyl units, making it a prodrug form of Adefovir. Based on these results, the investigators conducted a randomized controlled trial to test the hypothesis that adefovir treatment would reduce or postpone the recurrence rate and improve the overall survival rate in patients after TACE treatment of HBV-related unresectable HCC.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatitis B Virus, Hepatocellular Carcinoma
Keywords
HBV-related unresectable HCC, TACE, adefovir, recurrence rate

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
216 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
TACE
Arm Type
Placebo Comparator
Arm Description
An emulsion that consisted of 50 mg of cisplatin and 10 mL of lipiodol at a volume ratio of 1:1 was injected into the blood supply artery of the tumor under fluoroscopic guidance. The injection could be slowed or discontinued if retrograde flow occurred. Embolization was subsequently performed with granules of gelatin sponge particles.
Arm Title
TACE+adefovir
Arm Type
Experimental
Arm Description
patients received adefovir, at a dose of 10 mg daily after TACE treatment, for 48 weeks
Intervention Type
Drug
Intervention Name(s)
adefovir
Intervention Description
adefovir at 10 mg daily for 48 weeks
Intervention Type
Procedure
Intervention Name(s)
TACE
Intervention Description
An emulsion that consisted of 50 mg of cisplatin and 10 mL of lipiodol at a volume ratio of 1:1 was injected into the blood supply artery of the tumor under fluoroscopic guidance. The injection could be slowed or discontinued if retrograde flow occurred. Embolization was subsequently performed with granules of gelatin sponge particles.
Primary Outcome Measure Information:
Title
the progression free survival (PFS)
Time Frame
3 months
Secondary Outcome Measure Information:
Title
the rate of overall survival
Time Frame
1, 3, 5 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: age:20-75 years old with a clinical diagnosis of primary liver cancer, with HBsAg positive,without any therapy for tumor single lesion with a diameter >6.5 cm,or multiple lesions locating within half liver or adjacent three lobe estimated liver remnant volume ≤40% with a liver function of Child-Pugh class A,and ALT≤80IU/l. Exclusion Criteria: reject to attend portal vein trunk has been compressed by tumor diffuse type cancer or with extensive cancer thrombus in main branches of PV,HV,IVC or bile duct with extrahepatic metastasis with obvious portal hypertension (with moderate to severe varix in esophagus and/or gastric fundus, enlarged spleen,WBC<4×109/L, PLT<80×109/L) with diabetes allergy to iodine
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Daoyuan Wang, MD
Phone
+86-21-6630058
Email
ghealth2008@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Maoquan Li, MD, PhD
Organizational Affiliation
Interventional Radiology Research Group, Shanghai Radiology Society
Official's Role
Study Chair
Facility Information:
Facility Name
The Fourth Affiliated Hospital of Haerbin Medical University
City
Ha'er'bin
State/Province
Heilongjiang
ZIP/Postal Code
150001
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Baozhong Shen, MD
Phone
+86-451-82576888
Email
drbaozhong.shen@gmail.com
First Name & Middle Initial & Last Name & Degree
Baozhong Shen, MD
Facility Name
Shanghai 10th Hospital of Tongji University
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200025
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Maoquan Li, MD, PhD
Phone
+86-21-6630058
Email
drmaoquan.li@gmail.com
First Name & Middle Initial & Last Name & Degree
Maoquan Li, MD, PhD

12. IPD Sharing Statement

Citations:
PubMed Identifier
19486255
Citation
Li M, Lu C, Cheng J, Zhang J, Cao C, Xu J, Xu J, Pan H, Zhong B, Tucker S, Wang D. Combination therapy with transarterial chemoembolization and interferon-alpha compared with transarterial chemoembolization alone for hepatitis B virus related unresectable hepatocellular carcinoma. J Gastroenterol Hepatol. 2009 Aug;24(8):1437-44. doi: 10.1111/j.1440-1746.2009.05863.x. Epub 2009 May 28.
Results Reference
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TACE and Adefovir Compared With Transarterial Chemoembolization (TACE) Alone for Hepatitis B Virus (HBV)-Related Unresectable Hepatocellular Carcinoma (HCC)

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