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How to optimize hepatitis C virus treatment impact on life years saved in resource-constrained countries.

Identifieur interne : 002B03 ( PubMed/Checkpoint ); précédent : 002B02; suivant : 002B04

How to optimize hepatitis C virus treatment impact on life years saved in resource-constrained countries.

Auteurs : Dorothée Obach [France] ; Yazdan Yazdanpanah [France] ; Gamal Esmat [Égypte] ; Anchalee Avihingsanon [Thaïlande] ; Sahar Dewedar [Égypte] ; Nicolas Durier [Thaïlande] ; Alain Attia [Côte d'Ivoire] ; Wagida A. Anwar [Égypte] ; Anthony Cousien [France] ; Pisit Tangkijvanich [Thaïlande] ; Serge Paul Eholié [Côte d'Ivoire] ; Wahid Doss [Égypte] ; Aya Mostafa [Égypte] ; Arnaud Fontanet [France] ; Mostafa K. Mohamed [Égypte] ; Sylvie Deuffic-Burban [France]

Source :

RBID : pubmed:25581111

Descripteurs français

English descriptors

Abstract

In resource-constrained countries where the prevalence of hepatitis C virus (HCV) disease is usually high, it is important to know which population should be treated first in order to increase treatment effectiveness. The aim was to estimate the effectiveness of different HCV treatment eligibility scenarios in three different countries. Using a Markov model, we estimated the number of life-years saved (LYS) with different treatment eligibility scenarios according to fibrosis stage (F1-F4 or F3-4), compared to base case (F2-F4), at a constant treatment rate, of patients between 18 and 60 years of age, at stages F0/F1 to F4, without liver complications or coinfections, chronically infected by HCV, and treated with pegylated interferon (IFN)/ribavirin or more-efficacious therapies (i.e. IFN free). We conducted the analysis in Egypt (prevalence = 14.7%; 45,000 patients treated/year), Thailand (prevalence = 2.2%; 1,000 patients treated/year), and Côte d'Ivoire (prevalence = 3%; 150 patients treated/year). In Egypt, treating F1 patients in addition to ≥F2 patients (SE1 vs. SE0) decreased LYS by 3.9%. Focusing treatment only on F3-F4 patients increased LYS by 6.7% (SE2 vs. SE0). In Thailand and Côte d'Ivoire, focusing treatment only on F3-F4 patients increased LYS by 15.3% and 11.0%, respectively, compared to treating patients ≥F2 (ST0 and SC0, respectively). Treatment only for patients at stages F3-F4 with IFN-free therapies would increase LYS by 16.7% versus SE0 in Egypt, 22.0% versus ST0 in Thailand, and 13.1% versus SC0 in Côte d'Ivoire. In this study, we did not take into account the yearly new infections and the impact of treatment on HCV transmission.

DOI: 10.1002/hep.27691
PubMed: 25581111


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pubmed:25581111

Le document en format XML

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<name sortKey="Durier, Nicolas" sort="Durier, Nicolas" uniqKey="Durier N" first="Nicolas" last="Durier">Nicolas Durier</name>
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<nlm:affiliation>TREAT Asia, amfAR-The Foundation for AIDS Research, Bangkok, Thailand.</nlm:affiliation>
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<name sortKey="Tangkijvanich, Pisit" sort="Tangkijvanich, Pisit" uniqKey="Tangkijvanich P" first="Pisit" last="Tangkijvanich">Pisit Tangkijvanich</name>
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<nlm:affiliation>Department of Biochemistry, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.</nlm:affiliation>
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<name sortKey="Eholie, Serge Paul" sort="Eholie, Serge Paul" uniqKey="Eholie S" first="Serge Paul" last="Eholié">Serge Paul Eholié</name>
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<nlm:affiliation>Service des Maladies Infectieuses et Tropicales, Centre Hospitalier Universitaire de Treichville, Abidjan, Côte d'Ivoire.</nlm:affiliation>
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<name sortKey="Doss, Wahid" sort="Doss, Wahid" uniqKey="Doss W" first="Wahid" last="Doss">Wahid Doss</name>
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<name sortKey="Mostafa, Aya" sort="Mostafa, Aya" uniqKey="Mostafa A" first="Aya" last="Mostafa">Aya Mostafa</name>
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<name sortKey="Fontanet, Arnaud" sort="Fontanet, Arnaud" uniqKey="Fontanet A" first="Arnaud" last="Fontanet">Arnaud Fontanet</name>
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<name sortKey="Mohamed, Mostafa K" sort="Mohamed, Mostafa K" uniqKey="Mohamed M" first="Mostafa K" last="Mohamed">Mostafa K. Mohamed</name>
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<nlm:affiliation>Department of Community, Environmental and Occupational Medicine, Faculty of Medicine, Ain Shams University, Cairo, Egypt.</nlm:affiliation>
<country xml:lang="fr">Égypte</country>
<wicri:regionArea>Department of Community, Environmental and Occupational Medicine, Faculty of Medicine, Ain Shams University, Cairo</wicri:regionArea>
<wicri:noRegion>Cairo</wicri:noRegion>
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<name sortKey="Deuffic Burban, Sylvie" sort="Deuffic Burban, Sylvie" uniqKey="Deuffic Burban S" first="Sylvie" last="Deuffic-Burban">Sylvie Deuffic-Burban</name>
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<nlm:affiliation>Inserm UMR 1137, IAME, F-75018 Paris, France; Université Paris Diderot, Sorbonne Paris Cité, Paris, France.</nlm:affiliation>
<country xml:lang="fr">France</country>
<wicri:regionArea>Inserm UMR 1137, IAME, F-75018 Paris, France; Université Paris Diderot, Sorbonne Paris Cité, Paris</wicri:regionArea>
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<title level="j">Hepatology (Baltimore, Md.)</title>
<idno type="eISSN">1527-3350</idno>
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<date when="2015" type="published">2015</date>
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<term>Antiviral Agents (therapeutic use)</term>
<term>Cost-Benefit Analysis</term>
<term>Developing Countries</term>
<term>Hepatitis C (complications)</term>
<term>Hepatitis C (drug therapy)</term>
<term>Humans</term>
<term>Liver Cirrhosis (virology)</term>
<term>Models, Theoretical</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Analyse coût-bénéfice</term>
<term>Antiviraux (usage thérapeutique)</term>
<term>Cirrhose du foie (virologie)</term>
<term>Humains</term>
<term>Hépatite C ()</term>
<term>Hépatite C (traitement médicamenteux)</term>
<term>Modèles théoriques</term>
<term>Pays en voie de développement</term>
</keywords>
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<term>Antiviral Agents</term>
</keywords>
<keywords scheme="MESH" qualifier="complications" xml:lang="en">
<term>Hepatitis C</term>
</keywords>
<keywords scheme="MESH" qualifier="drug therapy" xml:lang="en">
<term>Hepatitis C</term>
</keywords>
<keywords scheme="MESH" qualifier="traitement médicamenteux" xml:lang="fr">
<term>Hépatite C</term>
</keywords>
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<term>Antiviraux</term>
</keywords>
<keywords scheme="MESH" qualifier="virologie" xml:lang="fr">
<term>Cirrhose du foie</term>
</keywords>
<keywords scheme="MESH" qualifier="virology" xml:lang="en">
<term>Liver Cirrhosis</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Cost-Benefit Analysis</term>
<term>Developing Countries</term>
<term>Humans</term>
<term>Models, Theoretical</term>
</keywords>
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<term>Analyse coût-bénéfice</term>
<term>Humains</term>
<term>Hépatite C</term>
<term>Modèles théoriques</term>
<term>Pays en voie de développement</term>
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<div type="abstract" xml:lang="en">In resource-constrained countries where the prevalence of hepatitis C virus (HCV) disease is usually high, it is important to know which population should be treated first in order to increase treatment effectiveness. The aim was to estimate the effectiveness of different HCV treatment eligibility scenarios in three different countries. Using a Markov model, we estimated the number of life-years saved (LYS) with different treatment eligibility scenarios according to fibrosis stage (F1-F4 or F3-4), compared to base case (F2-F4), at a constant treatment rate, of patients between 18 and 60 years of age, at stages F0/F1 to F4, without liver complications or coinfections, chronically infected by HCV, and treated with pegylated interferon (IFN)/ribavirin or more-efficacious therapies (i.e. IFN free). We conducted the analysis in Egypt (prevalence = 14.7%; 45,000 patients treated/year), Thailand (prevalence = 2.2%; 1,000 patients treated/year), and Côte d'Ivoire (prevalence = 3%; 150 patients treated/year). In Egypt, treating F1 patients in addition to ≥F2 patients (SE1 vs. SE0) decreased LYS by 3.9%. Focusing treatment only on F3-F4 patients increased LYS by 6.7% (SE2 vs. SE0). In Thailand and Côte d'Ivoire, focusing treatment only on F3-F4 patients increased LYS by 15.3% and 11.0%, respectively, compared to treating patients ≥F2 (ST0 and SC0, respectively). Treatment only for patients at stages F3-F4 with IFN-free therapies would increase LYS by 16.7% versus SE0 in Egypt, 22.0% versus ST0 in Thailand, and 13.1% versus SC0 in Côte d'Ivoire. In this study, we did not take into account the yearly new infections and the impact of treatment on HCV transmission.</div>
</front>
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<DateCreated>
<Year>2015</Year>
<Month>06</Month>
<Day>25</Day>
</DateCreated>
<DateCompleted>
<Year>2015</Year>
<Month>09</Month>
<Day>16</Day>
</DateCompleted>
<DateRevised>
<Year>2016</Year>
<Month>04</Month>
<Day>27</Day>
</DateRevised>
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<Journal>
<ISSN IssnType="Electronic">1527-3350</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>62</Volume>
<Issue>1</Issue>
<PubDate>
<Year>2015</Year>
<Month>Jul</Month>
</PubDate>
</JournalIssue>
<Title>Hepatology (Baltimore, Md.)</Title>
<ISOAbbreviation>Hepatology</ISOAbbreviation>
</Journal>
<ArticleTitle>How to optimize hepatitis C virus treatment impact on life years saved in resource-constrained countries.</ArticleTitle>
<Pagination>
<MedlinePgn>31-9</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1002/hep.27691</ELocationID>
<Abstract>
<AbstractText Label="UNLABELLED">In resource-constrained countries where the prevalence of hepatitis C virus (HCV) disease is usually high, it is important to know which population should be treated first in order to increase treatment effectiveness. The aim was to estimate the effectiveness of different HCV treatment eligibility scenarios in three different countries. Using a Markov model, we estimated the number of life-years saved (LYS) with different treatment eligibility scenarios according to fibrosis stage (F1-F4 or F3-4), compared to base case (F2-F4), at a constant treatment rate, of patients between 18 and 60 years of age, at stages F0/F1 to F4, without liver complications or coinfections, chronically infected by HCV, and treated with pegylated interferon (IFN)/ribavirin or more-efficacious therapies (i.e. IFN free). We conducted the analysis in Egypt (prevalence = 14.7%; 45,000 patients treated/year), Thailand (prevalence = 2.2%; 1,000 patients treated/year), and Côte d'Ivoire (prevalence = 3%; 150 patients treated/year). In Egypt, treating F1 patients in addition to ≥F2 patients (SE1 vs. SE0) decreased LYS by 3.9%. Focusing treatment only on F3-F4 patients increased LYS by 6.7% (SE2 vs. SE0). In Thailand and Côte d'Ivoire, focusing treatment only on F3-F4 patients increased LYS by 15.3% and 11.0%, respectively, compared to treating patients ≥F2 (ST0 and SC0, respectively). Treatment only for patients at stages F3-F4 with IFN-free therapies would increase LYS by 16.7% versus SE0 in Egypt, 22.0% versus ST0 in Thailand, and 13.1% versus SC0 in Côte d'Ivoire. In this study, we did not take into account the yearly new infections and the impact of treatment on HCV transmission.</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">Our model-based analysis demonstrates that prioritizing treatment in F3-F4 patients in resource-constrained countries is the most effective scenario in terms of LYS, regardless of treatment considered.</AbstractText>
<CopyrightInformation>© 2015 by the American Association for the Study of Liver Diseases.</CopyrightInformation>
</Abstract>
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<ForeName>Dorothée</ForeName>
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<AffiliationInfo>
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<AffiliationInfo>
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