Prophylactic Treatment of Hepatic Dysplastic Nodules in HBsAg Positive Patients
Primary Purpose
Dysplastic Nodule of Liver, Chronic Hepatitis B
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
minimally invasive ablation therapies
Sponsored by
About this trial
This is an interventional prevention trial for Dysplastic Nodule of Liver focused on measuring high grade dysplastic nodule (HGDN), low grade dysplastic nodule (LGDN)
Eligibility Criteria
Inclusion Criteria:
- Patients with chronic HBV
- Diagnosis of hepatic dysplastic nodule(s) be confirmed by biopsy.
Exclusion Criteria:
- concurrent HCV infection
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Ablation
Observation
Arm Description
Outcomes
Primary Outcome Measures
Incidence of hepatocellular carcinoma during the follow-up
The diagnosis of hepatocellular carcinoma during the follow-up will follow the AASLD practice guideline for the management of hepatocellular carcinoma (2010)
Secondary Outcome Measures
Full Information
NCT ID
NCT02793791
First Posted
May 31, 2016
Last Updated
June 2, 2016
Sponsor
Shandong Cancer Hospital and Institute
1. Study Identification
Unique Protocol Identification Number
NCT02793791
Brief Title
Prophylactic Treatment of Hepatic Dysplastic Nodules in HBsAg Positive Patients
Official Title
Prophylactic Minimally-invasive Local Ablation Therapies for the Hepatic Dysplastic Nodules in Patients With Positive Hepatitis B Surface Antigen (HBsAg).
Study Type
Interventional
2. Study Status
Record Verification Date
June 2016
Overall Recruitment Status
Unknown status
Study Start Date
September 2016 (undefined)
Primary Completion Date
December 2019 (Anticipated)
Study Completion Date
December 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Shandong Cancer Hospital and Institute
4. Oversight
5. Study Description
Brief Summary
The aim of this study is to determine that for hepatic dysplastic nodules in patients with chronic hepatitis B, instead of enhanced follow-up, whether early minimally-invasive ablation therapy can reduce the incidence of hepatocellular carcinoma.
Detailed Description
Hepatic dysplastic nodules (DNs) include high grade dysplastic nodules (HGDNs) and low grade dysplastic nodule (LGDNs), their incidences are high in patients with liver cirrhosis. Once diagnosed, all latest versions of the major guidelines recommend enhanced follow-up, and no treatment would be provided until the diagnosis of hepatocellular carcinoma (HCC) is established during the follow-up.
While on the other hand, mounting evidence shows that DNs have relatively high transition rate to progress to HCC. In 154 patients with chronic hepatitis and cirrhosis, Kobayashi et al. reported the annual transition rate of 20% for patients with HGDN and 10% for patients with LGDN. The 5-year cumulative transition rate from HGDN and LGDN was 80.8% and 30.2%, respectively. Even regenerative nodules (RNs) without dysplasia evolved into HCC in 12.4%.More recently, Sato et al. studied 68 large regenerative nodules (LRNs) and 20 DNs from 1,500 consecutive nodular lesions; the 50-month transition rate was 13.6% in LRNs and 40% in DNs. Earlier studies support these findings.
Adenomatous polyps are accepted precursors to colorectal cancer (CRC) and removed to prevent cancer. Compared to the above transition rates, A recent cohort study estimated that the average annual transition rate from advanced adenoma to CRC in men was 3.1%,so the 5-year-transition rate was around 15%. Since the transition rate of hepatic DNs is much higher than the colorectal adenomatous polyps, is "enhanced follow-up" really the best choice of the treatment?
So in this proposed clinical trial, we hypothesize that for hepatic DNs discovered in patients with chronic hepatitis B, early minimally-invasive ablation treatment will decrease the incidence of HCC.
Recruited patients will be divided in to two groups randomly, in the "Observation group", patients will be followed-up and receive no therapy; while in the "Ablation group", the DNs will be ablated by minimally-invasive ablation therapies, including RFA, PEI, MWA, etc. All patients will be followed-up according to the AASLD guideline. Then the incidence of HCC of the two arms will be compared.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dysplastic Nodule of Liver, Chronic Hepatitis B
Keywords
high grade dysplastic nodule (HGDN), low grade dysplastic nodule (LGDN)
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
30 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Ablation
Arm Type
Experimental
Arm Title
Observation
Arm Type
No Intervention
Intervention Type
Procedure
Intervention Name(s)
minimally invasive ablation therapies
Intervention Description
Including RFA (radiofrequency ablation);MWA (microwave ablation); PEI (percutaneous ethanol injection),etc.
Primary Outcome Measure Information:
Title
Incidence of hepatocellular carcinoma during the follow-up
Description
The diagnosis of hepatocellular carcinoma during the follow-up will follow the AASLD practice guideline for the management of hepatocellular carcinoma (2010)
Time Frame
Up to 70 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients with chronic HBV
Diagnosis of hepatic dysplastic nodule(s) be confirmed by biopsy.
Exclusion Criteria:
concurrent HCV infection
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Lei Zhao, MD
Phone
+8653167626368
Email
drzhaolei@hotmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lei Zhao, MD
Organizational Affiliation
Shandong Cancer Hospital and Institute
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
PubMed Identifier
21374666
Citation
Bruix J, Sherman M; American Association for the Study of Liver Diseases. Management of hepatocellular carcinoma: an update. Hepatology. 2011 Mar;53(3):1020-2. doi: 10.1002/hep.24199. No abstract available.
Results Reference
background
PubMed Identifier
22424278
Citation
European Association for Study of Liver; European Organisation for Research and Treatment of Cancer. EASL-EORTC clinical practice guidelines: management of hepatocellular carcinoma. Eur J Cancer. 2012 Mar;48(5):599-641. doi: 10.1016/j.ejca.2011.12.021. No abstract available. Erratum In: Eur J Cancer. 2012 May;48(8):1255-6.
Results Reference
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PubMed Identifier
16369988
Citation
Kobayashi M, Ikeda K, Hosaka T, Sezaki H, Someya T, Akuta N, Suzuki F, Suzuki Y, Saitoh S, Arase Y, Kumada H. Dysplastic nodules frequently develop into hepatocellular carcinoma in patients with chronic viral hepatitis and cirrhosis. Cancer. 2006 Feb 1;106(3):636-47. doi: 10.1002/cncr.21607.
Results Reference
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PubMed Identifier
25788204
Citation
Sato T, Kondo F, Ebara M, Sugiura N, Okabe S, Sunaga M, Yoshikawa M, Suzuki E, Ogasawara S, Shinozaki Y, Ooka Y, Chiba T, Kanai F, Kishimoto T, Nakatani Y, Fukusato T, Yokosuka O. Natural history of large regenerative nodules and dysplastic nodules in liver cirrhosis: 28-year follow-up study. Hepatol Int. 2015 Apr;9(2):330-6. doi: 10.1007/s12072-015-9620-6. Epub 2015 Mar 3.
Results Reference
background
PubMed Identifier
23632815
Citation
Brenner H, Altenhofen L, Stock C, Hoffmeister M. Natural history of colorectal adenomas: birth cohort analysis among 3.6 million participants of screening colonoscopy. Cancer Epidemiol Biomarkers Prev. 2013 Jun;22(6):1043-51. doi: 10.1158/1055-9965.EPI-13-0162. Epub 2013 Apr 30.
Results Reference
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Prophylactic Treatment of Hepatic Dysplastic Nodules in HBsAg Positive Patients
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