Relative efficacy and safety of simeprevir and telaprevir in treatment‐naïve hepatitis C‐infected patients in a Japanese population: A Bayesian network meta‐analysis. Issue 10 (3rd March 2015)
- Record Type:
- Journal Article
- Title:
- Relative efficacy and safety of simeprevir and telaprevir in treatment‐naïve hepatitis C‐infected patients in a Japanese population: A Bayesian network meta‐analysis. Issue 10 (3rd March 2015)
- Main Title:
- Relative efficacy and safety of simeprevir and telaprevir in treatment‐naïve hepatitis C‐infected patients in a Japanese population: A Bayesian network meta‐analysis
- Authors:
- Quigley, Joan M.
Bryden, Peter A.
Scott, David A.
Kuwabara, Hiroyo
Cerri, Karin - Abstract:
- Abstract : Aim: Simeprevir (SMV) is an oral, once‐daily protease inhibitor for the treatment of chronic hepatitis C virus (HCV) genotype 1 infection. In phase II/III randomized controlled trials (RCT) conducted in Japan, SMV, in combination with peginterferon‐α and ribavirin (PEG IFN/RBV), demonstrated potent efficacy in HCV genotype 1‐infected patients relative to PEG IFN/RBV and was generally well tolerated. Telaprevir (TVR) in combination with PEG IFN/RBV is licensed for the treatment of HCV in Japan. In the absence of head‐to‐head comparisons of TVR and SMV in a Japanese population, we undertook a network meta‐analysis (NMA) to examine the relative efficacy and safety of SMV and TVR in combination with PEG IFN/RBV. Methods: A systematic review identified SMV and TVR RCT in Japanese treatment‐naïve patients. Bayesian NMA was performed assuming fixed study effects. Results: Three studies met our inclusion criteria: two SMV and one TVR. SMV showed a higher mean odds ratio (OR) of achieving SVR versus TVR (OR, 1.68 (95% credible interval 0.66–4.26)). SMV showed a lower mean OR of discontinuation: overall, 0.35 (0.12–1.00); and due to AE, 0.87 (0.23–3.34) versus TVR. SMV showed a lower mean OR of experiencing anemia 0.20 (0.07–0.56) and rash 0.41 (0.17–0.99) but a higher mean OR of experiencing pruritus 1.26 (0.46–3.47) versus TVR. Conclusion: In this indirect treatment comparison, SMV, in combination with PEG IFN/RBV, showed a favorable risk–benefit profile compared with TVRAbstract : Aim: Simeprevir (SMV) is an oral, once‐daily protease inhibitor for the treatment of chronic hepatitis C virus (HCV) genotype 1 infection. In phase II/III randomized controlled trials (RCT) conducted in Japan, SMV, in combination with peginterferon‐α and ribavirin (PEG IFN/RBV), demonstrated potent efficacy in HCV genotype 1‐infected patients relative to PEG IFN/RBV and was generally well tolerated. Telaprevir (TVR) in combination with PEG IFN/RBV is licensed for the treatment of HCV in Japan. In the absence of head‐to‐head comparisons of TVR and SMV in a Japanese population, we undertook a network meta‐analysis (NMA) to examine the relative efficacy and safety of SMV and TVR in combination with PEG IFN/RBV. Methods: A systematic review identified SMV and TVR RCT in Japanese treatment‐naïve patients. Bayesian NMA was performed assuming fixed study effects. Results: Three studies met our inclusion criteria: two SMV and one TVR. SMV showed a higher mean odds ratio (OR) of achieving SVR versus TVR (OR, 1.68 (95% credible interval 0.66–4.26)). SMV showed a lower mean OR of discontinuation: overall, 0.35 (0.12–1.00); and due to AE, 0.87 (0.23–3.34) versus TVR. SMV showed a lower mean OR of experiencing anemia 0.20 (0.07–0.56) and rash 0.41 (0.17–0.99) but a higher mean OR of experiencing pruritus 1.26 (0.46–3.47) versus TVR. Conclusion: In this indirect treatment comparison, SMV, in combination with PEG IFN/RBV, showed a favorable risk–benefit profile compared with TVR with PEG IFN/RBV in Japanese treatment‐naïve HCV patients. … (more)
- Is Part Of:
- Hepatology research. Volume 45:Issue 10(2015:Oct.)
- Journal:
- Hepatology research
- Issue:
- Volume 45:Issue 10(2015:Oct.)
- Issue Display:
- Volume 45, Issue 10 (2015)
- Year:
- 2015
- Volume:
- 45
- Issue:
- 10
- Issue Sort Value:
- 2015-0045-0010-0000
- Page Start:
- E89
- Page End:
- E98
- Publication Date:
- 2015-03-03
- Subjects:
- hepatitis C -- network meta‐analysis -- simeprevir -- telaprevir
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/hepr.12467 ↗
- 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:
- 1238.xml