English hepatitis C registry data show high response rates to directly acting anti-virals, even if treatment is not completed
Autor: | David Mutimer, Yevedzo Ntuli, Ahmed M. El-Sharkawy, William Gelson, Kosh Agarwal, Ceri Townley, Daniel M. Forton, Kathryn Drysdale, Graham R. Foster, Faizel Mahomed, Jonathan P. Bestwick |
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Rok vydání: | 2020 |
Předmět: |
Cyclopropanes
Male Sustained Virologic Response Sofosbuvir chemistry.chemical_compound 0302 clinical medicine Medicine Anilides Pharmacology (medical) Registries 030212 general & internal medicine Young adult Aged 80 and over Sulfonamides Imidazoles Gastroenterology Valine Anti virals Hepatitis C Middle Aged Drug Combinations England Grazoprevir Female 030211 gastroenterology & hepatology Registry data Uridine Monophosphate medicine.drug Adult Ledipasvir medicine.medical_specialty Elbasvir Macrocyclic Compounds Adolescent Proline Lactams Macrocyclic Antiviral Agents Young Adult 03 medical and health sciences Quinoxalines Internal medicine Ribavirin Humans Aged Benzofurans Fluorenes Hepatology business.industry medicine.disease digestive system diseases chemistry Benzimidazoles Carbamates business |
Zdroj: | Alimentary Pharmacology & Therapeutics. 52:168-181 |
ISSN: | 0269-2813 |
DOI: | 10.1111/apt.15780 |
Popis: | Background In England, choice of hepatitis C therapy is determined by national contracts that change with time, facilitating comparisons between different regimens. England has a diverse population with hepatitis C including large proportions of uncommon viral genotypes. Aim To evaluate efficacy of directly acting anti-viral treatments for hepatitis C in England using real-world data from the national treatment registry. Methods Sustained virological response (SVR) rates 12 weeks after treatment completion for patients treated between 2014 and August 2018 who attended for SVR tests were analysed in univariate subgroups using Chi-squared tests. Multivariate models were constructed with clinically relevant variables to determine predictors of SVR and evaluate the impact of treatment regimens. Results SVR data were available on 14,603 treated patients. The overall SVR rate was 95.59% [95% CI 95.25%-95.91%]. Multivariable regression modelling in patients with genotype 1 infection showed that the odds of SVR with elbasvir/grazoprevir were higher than for those treated with sofosbuvir/ledipasvir (OR 1.891, 95% CI 1.072-3.336, P = 0.028). For genotype 3, we found no significant difference between any of the treatment regimens. Patients who completed at least one third of the planned treatment duration achieved SVR rates in excess of 80%. Conclusions All of the currently licensed hepatitis C direct-acting anti-viral regimens had similar efficacy (>95%) in an unselected population. Noncompletion of planned treatment duration still resulted in over 80% SVR rates provided that more than one third of treatment was completed. |
Databáze: | OpenAIRE |
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