Efficacy of daclatasvir plus asunaprevir in patients with hepatitis C virus infection undergoing and not undergoing hemodialysis. Issue 9 (17th May 2018)
- Record Type:
- Journal Article
- Title:
- Efficacy of daclatasvir plus asunaprevir in patients with hepatitis C virus infection undergoing and not undergoing hemodialysis. Issue 9 (17th May 2018)
- Main Title:
- Efficacy of daclatasvir plus asunaprevir in patients with hepatitis C virus infection undergoing and not undergoing hemodialysis
- Authors:
- Fujii, Hideki
Kimura, Hiroyuki
Kurosaki, Masayuki
Hasebe, Chitomi
Akahane, Takehiro
Yagisawa, Hitoshi
Kato, Keizo
Yoshida, Hideo
Itakura, Jun
Sakita, Shinya
Satou, Takashi
Okada, Kazuhiko
Kusakabe, Atsunori
Kojima, Yuji
Kondo, Masahiko
Morita, Atsuhiro
Nasu, Akihiro
Tamada, Takashi
Okushin, Hiroaki
Kobashi, Haruhiko
Tsuji, Keiji
Joko, Kouji
Ogawa, Chikara
Uchida, Yasushi
Mitsuda, Akeri
Sohda, Tetsuro
Ide, Yasushi
Izumi, Namiki - Abstract:
- Abstract : Aim: To evaluate the virologic responses and clinical course of daclatasvir plus asunaprevir treatment in non‐hemodialysis (non‐HD) and hemodialysis (HD) patients infected with genotype 1 hepatitis C virus (HCV). Methods: A total of 1113 non‐HD patients and 67 HD patients were assessed. To evaluate pretreatment factors contributing to sustained virological response at 12 weeks (SVR12), univariate and multivariate analyses were carried out. To adjust for differences in patient background, propensity score matching was undertaken. Results: The overall SVR12 rates were 91.6% in non‐HD patients and 95.5% in HD patients. Compared with non‐HD patients, HD patients were younger, were more likely to be male, were less likely to have received interferon‐based pretreatment, had a lower viral load, and had lower levels of alanine transaminase, hemoglobin, and α‐fetoprotein. Multivariate analysis revealed that viral load, α‐fetoprotein, L31 substitution negative, and Y93 substitution negative were independent predictive factors for SVR12 in non‐HD patients. The proportion of patients with undetectable HCV‐RNA during the initial 4 weeks was significantly higher in HD patients than in non‐HD patients. The SVR12 rate was clearly higher in HD patients than in non‐HD patients, although the difference was not statistically significant. After propensity score matching to adjust for viral load, α‐fetoprotein, L31 substitution, and Y93 substitution, these trends disappeared.Abstract : Aim: To evaluate the virologic responses and clinical course of daclatasvir plus asunaprevir treatment in non‐hemodialysis (non‐HD) and hemodialysis (HD) patients infected with genotype 1 hepatitis C virus (HCV). Methods: A total of 1113 non‐HD patients and 67 HD patients were assessed. To evaluate pretreatment factors contributing to sustained virological response at 12 weeks (SVR12), univariate and multivariate analyses were carried out. To adjust for differences in patient background, propensity score matching was undertaken. Results: The overall SVR12 rates were 91.6% in non‐HD patients and 95.5% in HD patients. Compared with non‐HD patients, HD patients were younger, were more likely to be male, were less likely to have received interferon‐based pretreatment, had a lower viral load, and had lower levels of alanine transaminase, hemoglobin, and α‐fetoprotein. Multivariate analysis revealed that viral load, α‐fetoprotein, L31 substitution negative, and Y93 substitution negative were independent predictive factors for SVR12 in non‐HD patients. The proportion of patients with undetectable HCV‐RNA during the initial 4 weeks was significantly higher in HD patients than in non‐HD patients. The SVR12 rate was clearly higher in HD patients than in non‐HD patients, although the difference was not statistically significant. After propensity score matching to adjust for viral load, α‐fetoprotein, L31 substitution, and Y93 substitution, these trends disappeared. Conclusions: For treatment of HCV genotype 1 infection, daclatasvir plus asunaprevir is useful not only in non‐HD patients but also in HD patients. Viral load, α‐fetoprotein levels, L31 substitution, and Y93 substitution influence treatment course and outcome. … (more)
- Is Part Of:
- Hepatology research. Volume 48:Issue 9(2018)
- Journal:
- Hepatology research
- Issue:
- Volume 48:Issue 9(2018)
- Issue Display:
- Volume 48, Issue 9 (2018)
- Year:
- 2018
- Volume:
- 48
- Issue:
- 9
- Issue Sort Value:
- 2018-0048-0009-0000
- Page Start:
- 746
- Page End:
- 756
- Publication Date:
- 2018-05-17
- Subjects:
- asunaprevir -- daclatasvir -- hemodialysis -- non‐hemodialysis -- propensity score matching
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.13070 ↗
- Languages:
- English
- ISSNs:
- 1386-6346
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4295.845000
British Library DSC - BLDSS-3PM
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- 7062.xml