Predictors of response to tenofovir disoproxil fumarate plus peginterferon alfa-2a combination therapy for chronic hepatitis B.
Identifieur interne : 003B44 ( Ncbi/Merge ); précédent : 003B43; suivant : 003B45Predictors of response to tenofovir disoproxil fumarate plus peginterferon alfa-2a combination therapy for chronic hepatitis B.
Auteurs : P. Marcellin [France] ; S H Ahn [Corée du Sud] ; W-L Chuang [Taïwan] ; A J Hui [République populaire de Chine] ; F. Tabak [Turquie] ; R. Mehta [Inde] ; J. Petersen [Allemagne] ; C-M Lee [Taïwan] ; X. Ma [États-Unis] ; F A Caruntu [Roumanie] ; W Y Tak [Corée du Sud] ; M. Elkhashab [Canada] ; L. Lin [États-Unis] ; G. Wu [États-Unis] ; E B Martins [États-Unis] ; P. Charuworn [États-Unis] ; L J Yee [États-Unis] ; S G Lim ; G R Foster [Royaume-Uni] ; S. Fung [Canada] ; L. Morano [Espagne] ; D. Samuel [France] ; K. Agarwal [Royaume-Uni] ; R. Idilman [Turquie] ; S I Strasser [Australie] ; M. Buti [Espagne] ; G B Gaeta [Italie] ; G. Papatheodoridis [Grèce] ; R. Flisiak [Pologne] ; H L Y. Chan [République populaire de Chine]Source :
- Alimentary pharmacology & therapeutics [ 1365-2036 ] ; 2016.
Descripteurs français
- KwdFr :
- ADN viral (sang), Administration par voie orale, Adulte, Adulte d'âge moyen, Antigènes de surface du virus de l'hépatite B (sang), Antiviraux (administration et posologie), Association de médicaments, Femelle, Humains, Hépatite B chronique (diagnostic), Hépatite B chronique (traitement médicamenteux), Injections sous-cutanées, Interféron alpha (administration et posologie), Mâle, Polyéthylène glycols (administration et posologie), Protéines recombinantes (administration et posologie), Résultat thérapeutique, Ténofovir (administration et posologie), Valeur prédictive des tests, Virus de l'hépatite B (), Virus de l'hépatite B (génétique).
- MESH :
- administration et posologie : Antiviraux, Interféron alpha, Polyéthylène glycols, Protéines recombinantes, Ténofovir.
- diagnostic : Hépatite B chronique.
- génétique : Virus de l'hépatite B.
- sang : ADN viral, Antigènes de surface du virus de l'hépatite B.
- traitement médicamenteux : Hépatite B chronique.
- Administration par voie orale, Adulte, Adulte d'âge moyen, Association de médicaments, Femelle, Humains, Injections sous-cutanées, Mâle, Résultat thérapeutique, Valeur prédictive des tests, Virus de l'hépatite B.
English descriptors
- KwdEn :
- Administration, Oral, Adult, Antiviral Agents (administration & dosage), DNA, Viral (blood), Drug Therapy, Combination, Female, Hepatitis B Surface Antigens (blood), Hepatitis B virus (drug effects), Hepatitis B virus (genetics), Hepatitis B, Chronic (diagnosis), Hepatitis B, Chronic (drug therapy), Humans, Injections, Subcutaneous, Interferon-alpha (administration & dosage), Male, Middle Aged, Polyethylene Glycols (administration & dosage), Predictive Value of Tests, Recombinant Proteins (administration & dosage), Tenofovir (administration & dosage), Treatment Outcome.
- MESH :
- chemical , administration & dosage : Antiviral Agents, Interferon-alpha, Polyethylene Glycols, Recombinant Proteins, Tenofovir.
- chemical , blood : DNA, Viral, Hepatitis B Surface Antigens.
- diagnosis : Hepatitis B, Chronic.
- drug effects : Hepatitis B virus.
- drug therapy : Hepatitis B, Chronic.
- genetics : Hepatitis B virus.
- Administration, Oral, Adult, Drug Therapy, Combination, Female, Humans, Injections, Subcutaneous, Male, Middle Aged, Predictive Value of Tests, Treatment Outcome.
Abstract
In patients with chronic hepatitis B, tenofovir disoproxil fumarate (TDF) plus pegylated interferon (PEG-IFN) for 48-weeks results in higher rates of hepatitis B surface antigen (HBsAg) loss than either monotherapy.
DOI: 10.1111/apt.13779
PubMed: 27629859
Links toward previous steps (curation, corpus...)
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pubmed:27629859Le document en format XML
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<sourceDesc><biblStruct><analytic><title xml:lang="en">Predictors of response to tenofovir disoproxil fumarate plus peginterferon alfa-2a combination therapy for chronic hepatitis B.</title>
<author><name sortKey="Marcellin, P" sort="Marcellin, P" uniqKey="Marcellin P" first="P" last="Marcellin">P. Marcellin</name>
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<author><name sortKey="Ahn, S H" sort="Ahn, S H" uniqKey="Ahn S" first="S H" last="Ahn">S H Ahn</name>
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<country xml:lang="fr">Corée du Sud</country>
<wicri:regionArea>Seoul</wicri:regionArea>
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<author><name sortKey="Chuang, W L" sort="Chuang, W L" uniqKey="Chuang W" first="W-L" last="Chuang">W-L Chuang</name>
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<author><name sortKey="Hui, A J" sort="Hui, A J" uniqKey="Hui A" first="A J" last="Hui">A J Hui</name>
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<author><name sortKey="Tabak, F" sort="Tabak, F" uniqKey="Tabak F" first="F" last="Tabak">F. Tabak</name>
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<author><name sortKey="Mehta, R" sort="Mehta, R" uniqKey="Mehta R" first="R" last="Mehta">R. Mehta</name>
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<author><name sortKey="Petersen, J" sort="Petersen, J" uniqKey="Petersen J" first="J" last="Petersen">J. Petersen</name>
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<author><name sortKey="Ma, X" sort="Ma, X" uniqKey="Ma X" first="X" last="Ma">X. Ma</name>
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<author><name sortKey="Caruntu, F A" sort="Caruntu, F A" uniqKey="Caruntu F" first="F A" last="Caruntu">F A Caruntu</name>
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<author><name sortKey="Martins, E B" sort="Martins, E B" uniqKey="Martins E" first="E B" last="Martins">E B Martins</name>
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<author><name sortKey="Charuworn, P" sort="Charuworn, P" uniqKey="Charuworn P" first="P" last="Charuworn">P. Charuworn</name>
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<author><name sortKey="Yee, L J" sort="Yee, L J" uniqKey="Yee L" first="L J" last="Yee">L J Yee</name>
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<author><name sortKey="Lim, S G" sort="Lim, S G" uniqKey="Lim S" first="S G" last="Lim">S G Lim</name>
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<author><name sortKey="Foster, G R" sort="Foster, G R" uniqKey="Foster G" first="G R" last="Foster">G R Foster</name>
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<front><div type="abstract" xml:lang="en">In patients with chronic hepatitis B, tenofovir disoproxil fumarate (TDF) plus pegylated interferon (PEG-IFN) for 48-weeks results in higher rates of hepatitis B surface antigen (HBsAg) loss than either monotherapy.</div>
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<DateCreated><Year>2016</Year>
<Month>09</Month>
<Day>15</Day>
</DateCreated>
<DateCompleted><Year>2017</Year>
<Month>08</Month>
<Day>29</Day>
</DateCompleted>
<DateRevised><Year>2017</Year>
<Month>08</Month>
<Day>29</Day>
</DateRevised>
<Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1365-2036</ISSN>
<JournalIssue CitedMedium="Internet"><Volume>44</Volume>
<Issue>9</Issue>
<PubDate><Year>2016</Year>
<Month>Nov</Month>
</PubDate>
</JournalIssue>
<Title>Alimentary pharmacology & therapeutics</Title>
<ISOAbbreviation>Aliment. Pharmacol. Ther.</ISOAbbreviation>
</Journal>
<ArticleTitle>Predictors of response to tenofovir disoproxil fumarate plus peginterferon alfa-2a combination therapy for chronic hepatitis B.</ArticleTitle>
<Pagination><MedlinePgn>957-966</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1111/apt.13779</ELocationID>
<Abstract><AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">In patients with chronic hepatitis B, tenofovir disoproxil fumarate (TDF) plus pegylated interferon (PEG-IFN) for 48-weeks results in higher rates of hepatitis B surface antigen (HBsAg) loss than either monotherapy.</AbstractText>
<AbstractText Label="AIM" NlmCategory="OBJECTIVE">To identify baseline and on-treatment factors associated with HBsAg loss at Week 72 and provide a model for predicting HBsAg loss in patients receiving combination therapy for 48 weeks.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">A secondary analysis of data from an open-label study where patients were randomised to TDF (300 mg/day, oral) plus PEG-IFN (PI, 180 μg/week, subcutaneous) for 48 weeks (TDF/PI-48w); TDF plus PEG-IFN for 16 weeks, TDF for 32 weeks (TDF/PI-16w+TDF-32w); TDF for 120 weeks (TDF-120w) or PEG-IFN for 48 weeks (PI-48w). Logistic regression methods were used to identify models that best predicted HBsAg loss at Week 72.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Rates of HBsAg loss at Week 72 were significantly higher in the TDF/PI-48w group (6.5%) than in the TDF/PI-16w+TDF-32w (0.5%), TDF-120w (0%) and PI-48w (2.2%) groups (P = 0.09). The only baseline factor associated with response was genotype A. HBsAg decline at Week 12 or 24 of treatment was associated with HBsAg loss at Week 72 (P < 0.001). HBsAg decline >3.5 log10 IU/mL at Week 24 in the TDF/PI-48w group resulted in a positive predictive value of 85% and a negative predictive value of 99% for HBsAg loss at Week 72.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">HBsAg decline at Week 24 of TDF plus PEG-IFN combination therapy may identify patients who, after completing 48 weeks of treatment, have a better chance of achieving HBsAg loss at Week 72.</AbstractText>
<CopyrightInformation>© 2016 John Wiley & Sons Ltd.</CopyrightInformation>
</Abstract>
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<Author ValidYN="Y"><LastName>Foster</LastName>
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