Long‐term entecavir or tenofovir disoproxil fumarate therapy in treatment‐naïve chronic hepatitis B patients in the real‐world setting. Issue 5 (28th November 2014)
- Record Type:
- Journal Article
- Title:
- Long‐term entecavir or tenofovir disoproxil fumarate therapy in treatment‐naïve chronic hepatitis B patients in the real‐world setting. Issue 5 (28th November 2014)
- Main Title:
- Long‐term entecavir or tenofovir disoproxil fumarate therapy in treatment‐naïve chronic hepatitis B patients in the real‐world setting
- Authors:
- Idilman, R.
Gunsar, F.
Koruk, M.
Keskin, O.
Meral, C. E.
Gulsen, M.
Elhan, A. H.
Akarca, U. S.
Yurdaydin, C. - Abstract:
- <abstract abstract-type="main" id="jvh12358-abs-0001"> <title>Summary</title> <p>The aim of this study was to determine the long‐term efficacy of entecavir (ETV) and tenofovir disoproxil fumarate (TDF) on the natural course of disease in chronic hepatitis B patients (CHB) with/without cirrhosis in clinical practice. A total of 355 treatment‐naïve CHB patients were enrolled into the study. The primary outcome measure was viral suppression as defined by serum HBV DNA level &lt;20 IU/mL. A secondary outcome measure was to determine the development of Hepatocellular carcinoma (HCC). Virological and biochemical responses were similar between the two treatment groups over time. The presence of cirrhosis and hepatitis B e antigen (HBeAg) positivity did not appear to impact viral suppression. The cumulative probability of HBeAg loss was 41% at 4 years of therapy. Hepatitis B surface antigen (HBsAg) loss occurred in four patients. Model for End‐Stage Liver Disease score was significantly improved from baseline to week 48 and 96 under antiviral therapy (<italic>P</italic> = 0.013, <italic>P</italic> = 0.01). HCC was diagnosed in 17 patients (4.8%). The cumulative probability of the development of HCC was 3.3% at 1 year and 7.3% at 4 years of therapy. The development of HCC was independently associated with older age (<italic>P</italic> = 0.031) and the presence of cirrhosis (<italic>P</italic> = 0.004). Serum creatinine levels and creatinine clearance remained stable over time. ETV<abstract abstract-type="main" id="jvh12358-abs-0001"> <title>Summary</title> <p>The aim of this study was to determine the long‐term efficacy of entecavir (ETV) and tenofovir disoproxil fumarate (TDF) on the natural course of disease in chronic hepatitis B patients (CHB) with/without cirrhosis in clinical practice. A total of 355 treatment‐naïve CHB patients were enrolled into the study. The primary outcome measure was viral suppression as defined by serum HBV DNA level &lt;20 IU/mL. A secondary outcome measure was to determine the development of Hepatocellular carcinoma (HCC). Virological and biochemical responses were similar between the two treatment groups over time. The presence of cirrhosis and hepatitis B e antigen (HBeAg) positivity did not appear to impact viral suppression. The cumulative probability of HBeAg loss was 41% at 4 years of therapy. Hepatitis B surface antigen (HBsAg) loss occurred in four patients. Model for End‐Stage Liver Disease score was significantly improved from baseline to week 48 and 96 under antiviral therapy (<italic>P</italic> = 0.013, <italic>P</italic> = 0.01). HCC was diagnosed in 17 patients (4.8%). The cumulative probability of the development of HCC was 3.3% at 1 year and 7.3% at 4 years of therapy. The development of HCC was independently associated with older age (<italic>P</italic> = 0.031) and the presence of cirrhosis (<italic>P</italic> = 0.004). Serum creatinine levels and creatinine clearance remained stable over time. ETV and TDF effectively maintained virological and biochemical responses in long‐term follow‐up of CHB patients with/without cirrhosis. HCC may still develop, although at a lower rate, and is more likely to develop in patients with cirrhosis, especially in older patients.</p> </abstract> … (more)
- Is Part Of:
- Journal of viral hepatitis. Volume 22:Issue 5(2015)
- Journal:
- Journal of viral hepatitis
- Issue:
- Volume 22:Issue 5(2015)
- Issue Display:
- Volume 22, Issue 5 (2015)
- Year:
- 2015
- Volume:
- 22
- Issue:
- 5
- Issue Sort Value:
- 2015-0022-0005-0000
- Page Start:
- 504
- Page End:
- 510
- Publication Date:
- 2014-11-28
- Subjects:
- Hepatitis, Viral -- Periodicals
Hepatitis, Viral, Animal
Hepatitis, Viral, Human
616.3623 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-2893 ↗
http://www.blackwell-synergy.com/member/institutions/issuelist.asp?journal=jvh ↗
http://onlinelibrary.wiley.com/ ↗
http://firstsearch.oclc.org ↗
http://firstsearch.oclc.org/journal=1352-0504;screen=info;ECOIP ↗ - DOI:
- 10.1111/jvh.12358 ↗
- Languages:
- English
- ISSNs:
- 1352-0504
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5072.485500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3373.xml