A multicenter survey of re‐treatment with pegylated interferon plus ribavirin combination therapy for patients with chronic hepatitis C in Japan. Issue 1 (18th January 2013)
- Record Type:
- Journal Article
- Title:
- A multicenter survey of re‐treatment with pegylated interferon plus ribavirin combination therapy for patients with chronic hepatitis C in Japan. Issue 1 (18th January 2013)
- Main Title:
- A multicenter survey of re‐treatment with pegylated interferon plus ribavirin combination therapy for patients with chronic hepatitis C in Japan
- Authors:
- Oze, Tsugiko
Hiramatsu, Naoki
Mita, Eiji
Akuta, Norio
Sakamoto, Naoya
Nagano, Hiroaki
Itoh, Yoshito
Kaneko, Shuichi
Izumi, Namiki
Nomura, Hideyuki
Hayashi, Norio
Takehara, Tetsuo - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <p> <bold>Aim: </bold> This study aimed to clarify the factors associated the efficacy of re‐treatment with pegylated interferon (PEG IFN) plus ribavirin combination therapy for patients with chronic hepatitis C who had failed to respond to previous treatment.</p> <p> <bold>Methods: </bold> One hundred and forty‐three patients who had previously shown relapse (<italic>n</italic> = 79), non‐response (<italic>n</italic> = 34) or intolerance (<italic>n</italic> = 30) to PEG IFN plus ribavirin were re‐treated with PEG IFN plus ribavirin.</p> <p> <bold>Results: </bold> Twenty‐five patients with intolerance to previous treatment completed re‐treatment and the sustained virological response (SVR) rates were 55% and 80% for hepatitis C virus (HCV) genotype 1 and 2, respectively. On re‐treatment of the 113 patients who completed the previous treatment, the SVR rates were 48% and 63% for genotype 1 and 2, respectively. Relapse after previous treatment and a low baseline HCV RNA level on re‐treatment were associated with SVR in genotype 1 (<italic>P</italic> &lt; 0.001). Patients with the interleukin‐28B major genotype responded significantly better and earlier to re‐treatment, but the difference in the SVR rate did not reach a significant level between the major and minor genotypes (<italic>P</italic> = 0.09). Extended treatment of 72 weeks raised the SVR rate among the patients who<abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <p> <bold>Aim: </bold> This study aimed to clarify the factors associated the efficacy of re‐treatment with pegylated interferon (PEG IFN) plus ribavirin combination therapy for patients with chronic hepatitis C who had failed to respond to previous treatment.</p> <p> <bold>Methods: </bold> One hundred and forty‐three patients who had previously shown relapse (<italic>n</italic> = 79), non‐response (<italic>n</italic> = 34) or intolerance (<italic>n</italic> = 30) to PEG IFN plus ribavirin were re‐treated with PEG IFN plus ribavirin.</p> <p> <bold>Results: </bold> Twenty‐five patients with intolerance to previous treatment completed re‐treatment and the sustained virological response (SVR) rates were 55% and 80% for hepatitis C virus (HCV) genotype 1 and 2, respectively. On re‐treatment of the 113 patients who completed the previous treatment, the SVR rates were 48% and 63% for genotype 1 and 2, respectively. Relapse after previous treatment and a low baseline HCV RNA level on re‐treatment were associated with SVR in genotype 1 (<italic>P</italic> &lt; 0.001). Patients with the interleukin‐28B major genotype responded significantly better and earlier to re‐treatment, but the difference in the SVR rate did not reach a significant level between the major and minor genotypes (<italic>P</italic> = 0.09). Extended treatment of 72 weeks raised the SVR rate among the patients who attained complete early virological response but not rapid virological response with re‐treatment (72 weeks, 73%, 16/22, vs 48 weeks, 38%, 5/13, <italic>P</italic> &lt; 0.05).</p> <p> <bold>Conclusion: </bold> Relapse after previous treatment and a low baseline HCV RNA level have predictive values for a favorable response of PEG IFN plus ribavirin re‐treatment for HCV genotype 1 patients. Re‐treatment for 72 weeks may lead to clinical improvement for genotype 1 patients with complete early virological response and without rapid virological response on re‐treatment.</p> </abstract> … (more)
- Is Part Of:
- Hepatology research. Volume 43:Issue 1(2013:Jan.)
- Journal:
- Hepatology research
- Issue:
- Volume 43:Issue 1(2013:Jan.)
- Issue Display:
- Volume 43, Issue 1 (2013)
- Year:
- 2013
- Volume:
- 43
- Issue:
- 1
- Issue Sort Value:
- 2013-0043-0001-0000
- Page Start:
- 35
- Page End:
- 43
- Publication Date:
- 2013-01-18
- Subjects:
- Liver -- Diseases -- Periodicals
Liver Diseases -- Periodicals
Foie -- Maladies -- Périodiques
616.362 - Journal URLs:
- http://www.sciencedirect.com/science/journal/09284346 ↗
http://firstsearch.oclc.org/journal=1386-6346;screen=info;ECOIP ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1872-034X ↗
http://www.sciencedirect.com/science/journal/13866346 ↗
http://www3.interscience.wiley.com/journal/118507311/home ↗
http://www.blackwell-synergy.com/rd.asp?goto=journal&code=hep ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/j.1872-034X.2012.01056.x ↗
- Languages:
- English
- ISSNs:
- 1386-6346
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4295.845000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3523.xml