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Efficacy, safety and patient-reported outcomes of combination etanercept and sulfasalazine versus etanercept alone in patients with rheumatoid arthritis: a double-blind randomised 2-year study

Identifieur interne : 001278 ( Main/Exploration ); précédent : 001277; suivant : 001279

Efficacy, safety and patient-reported outcomes of combination etanercept and sulfasalazine versus etanercept alone in patients with rheumatoid arthritis: a double-blind randomised 2-year study

Auteurs : B. Combe [France] ; C. Codreanu [Roumanie] ; U. Fiocco [Italie] ; M. Gaubitz [Allemagne] ; P P Geusens [Belgique, Pays-Bas] ; T K Kvien [Norvège] ; K. Pavelka [République tchèque] ; P N Sambrook [Australie] ; J S Smolen [Autriche] ; R. Khandker [États-Unis] ; A. Singh [États-Unis] ; J. Wajdula [États-Unis] ; S. Fatenejad [États-Unis]

Source :

RBID : PMC:2689524

Abstract

Objective:

To determine the efficacy and safety of etanercept and etanercept plus sulfasalazine versus sulfasalazine in patients with rheumatoid arthritis (RA) despite sulfasalazine therapy.

Methods:

Patients were randomly assigned to etanercept (25 mg twice weekly; sulfasalazine was discontinued at baseline), etanercept plus sulfasalazine (unchanged regimen of 2–3 g/day) or sulfasalazine in a double-blind, randomised, 2-year study in adult patients with active RA despite sulfasalazine therapy. Efficacy was assessed using the American College of Rheumatology criteria, disease activity scores (DAS) and patient-reported outcomes (PRO).

Results:

Demographic variables and baseline disease characteristics were comparable among treatment groups; mean DAS 5.1, 5.2 and 5.1 for etanercept (n  =  103), etanercept plus sulfasalazine (n  =  101) and sulfasalazine (n  =  50), respectively. Withdrawal due to lack of efficacy was highest with sulfasalazine (26 (52%) vs 6 (6%) for either etanercept group, p<0.001). Patients receiving etanercept or etanercept plus sulfasalazine had a more rapid initial response, which was sustained at 2 years, than those receiving sulfasalazine: mean DAS 2.8, 2.5 versus 4.5, respectively (p<0.05); ACR 20 response was achieved by 67%, 77% versus 34% of patients, respectively (p<0.01) Overall, PRO followed a similar pattern; a clinically significant improvement in health assessment questionnaire was achieved by 76%, 78% versus 40% of patients, respectively (p<0.01). Commonly reported adverse events occurring in the etanercept groups were injection site reactions and pharyngitis/laryngitis (p<0.01).

Conclusion:

Etanercept and etanercept plus sulfasalazine are efficacious for the long-term management of patients with RA. The addition of etanercept or substitution with etanercept should be considered as treatment options for patients not adequately responding to sulfasalazine.


Url:
DOI: 10.1136/ard.2007.087106
PubMed: 18794178
PubMed Central: 2689524


Affiliations:


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Le document en format XML

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<name sortKey="Combe, B" sort="Combe, B" uniqKey="Combe B" first="B" last="Combe">B. Combe</name>
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<addr-line>Biomedical Research Center, University Hasselt, Hasselt, Belgium</addr-line>
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<wicri:noRegion>Hasselt</wicri:noRegion>
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<nlm:aff id="aff6">
<addr-line>Department of Internal Medicine/Rheumatology, University Maastricht, Maastricht, The Netherlands</addr-line>
</nlm:aff>
<country xml:lang="fr">Pays-Bas</country>
<wicri:regionArea>Department of Internal Medicine/Rheumatology, University Maastricht, Maastricht</wicri:regionArea>
<wicri:noRegion>Maastricht</wicri:noRegion>
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<name sortKey="Kvien, T K" sort="Kvien, T K" uniqKey="Kvien T" first="T K" last="Kvien">T K Kvien</name>
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<nlm:aff id="aff7">
<addr-line>Department of Rheumatology, Diakonhjemmets Hospital, Oslo, Norway</addr-line>
</nlm:aff>
<country xml:lang="fr">Norvège</country>
<wicri:regionArea>Department of Rheumatology, Diakonhjemmets Hospital, Oslo</wicri:regionArea>
<wicri:noRegion>Oslo</wicri:noRegion>
</affiliation>
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<name sortKey="Pavelka, K" sort="Pavelka, K" uniqKey="Pavelka K" first="K" last="Pavelka">K. Pavelka</name>
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<addr-line>Institute of Rheumatology, Praha, Czech Republic</addr-line>
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<country xml:lang="fr">République tchèque</country>
<wicri:regionArea>Institute of Rheumatology, Praha</wicri:regionArea>
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<settlement type="city">Prague</settlement>
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<name sortKey="Sambrook, P N" sort="Sambrook, P N" uniqKey="Sambrook P" first="P N" last="Sambrook">P N Sambrook</name>
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<nlm:aff id="aff9">
<addr-line>Kolling Institute, University of Sydney, Sydney, Australia</addr-line>
</nlm:aff>
<country xml:lang="fr">Australie</country>
<wicri:regionArea>Kolling Institute, University of Sydney, Sydney</wicri:regionArea>
<placeName>
<settlement type="city">Sydney</settlement>
</placeName>
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<name sortKey="Smolen, J S" sort="Smolen, J S" uniqKey="Smolen J" first="J S" last="Smolen">J S Smolen</name>
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<addr-line>2nd Department of Medicine, Krankenhaus Lainz and Department of Rheumatology, Internal Medicine III, Medical University of Vienna, Vienna, Austria</addr-line>
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<wicri:regionArea>2nd Department of Medicine, Krankenhaus Lainz and Department of Rheumatology, Internal Medicine III, Medical University of Vienna, Vienna</wicri:regionArea>
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<name sortKey="Khandker, R" sort="Khandker, R" uniqKey="Khandker R" first="R" last="Khandker">R. Khandker</name>
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<addr-line>Wyeth Research, Collegeville, Pennsylvania, USA</addr-line>
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<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Wyeth Research, Collegeville, Pennsylvania</wicri:regionArea>
<placeName>
<region type="state">Pennsylvanie</region>
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<name sortKey="Singh, A" sort="Singh, A" uniqKey="Singh A" first="A" last="Singh">A. Singh</name>
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<addr-line>Wyeth Research, Collegeville, Pennsylvania, USA</addr-line>
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<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Wyeth Research, Collegeville, Pennsylvania</wicri:regionArea>
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<region type="state">Pennsylvanie</region>
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<name sortKey="Wajdula, J" sort="Wajdula, J" uniqKey="Wajdula J" first="J" last="Wajdula">J. Wajdula</name>
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<nlm:aff id="aff11">
<addr-line>Wyeth Research, Collegeville, Pennsylvania, USA</addr-line>
</nlm:aff>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Wyeth Research, Collegeville, Pennsylvania</wicri:regionArea>
<placeName>
<region type="state">Pennsylvanie</region>
</placeName>
</affiliation>
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<name sortKey="Fatenejad, S" sort="Fatenejad, S" uniqKey="Fatenejad S" first="S" last="Fatenejad">S. Fatenejad</name>
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<addr-line>Wyeth Research, Collegeville, Pennsylvania, USA</addr-line>
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<country xml:lang="fr">États-Unis</country>
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<series>
<title level="j">Annals of the Rheumatic Diseases</title>
<idno type="ISSN">0003-4967</idno>
<idno type="eISSN">1468-2060</idno>
<imprint>
<date when="2008">2008</date>
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<div type="abstract" xml:lang="en">
<sec>
<title>Objective:</title>
<p>To determine the efficacy and safety of etanercept and etanercept plus sulfasalazine versus sulfasalazine in patients with rheumatoid arthritis (RA) despite sulfasalazine therapy.</p>
</sec>
<sec>
<title>Methods:</title>
<p>Patients were randomly assigned to etanercept (25 mg twice weekly; sulfasalazine was discontinued at baseline), etanercept plus sulfasalazine (unchanged regimen of 2–3 g/day) or sulfasalazine in a double-blind, randomised, 2-year study in adult patients with active RA despite sulfasalazine therapy. Efficacy was assessed using the American College of Rheumatology criteria, disease activity scores (DAS) and patient-reported outcomes (PRO).</p>
</sec>
<sec>
<title>Results:</title>
<p>Demographic variables and baseline disease characteristics were comparable among treatment groups; mean DAS 5.1, 5.2 and 5.1 for etanercept (n  =  103), etanercept plus sulfasalazine (n  =  101) and sulfasalazine (n  =  50), respectively. Withdrawal due to lack of efficacy was highest with sulfasalazine (26 (52%) vs 6 (6%) for either etanercept group, p<0.001). Patients receiving etanercept or etanercept plus sulfasalazine had a more rapid initial response, which was sustained at 2 years, than those receiving sulfasalazine: mean DAS 2.8, 2.5 versus 4.5, respectively (p<0.05); ACR 20 response was achieved by 67%, 77% versus 34% of patients, respectively (p<0.01) Overall, PRO followed a similar pattern; a clinically significant improvement in health assessment questionnaire was achieved by 76%, 78% versus 40% of patients, respectively (p<0.01). Commonly reported adverse events occurring in the etanercept groups were injection site reactions and pharyngitis/laryngitis (p<0.01).</p>
</sec>
<sec>
<title>Conclusion:</title>
<p>Etanercept and etanercept plus sulfasalazine are efficacious for the long-term management of patients with RA. The addition of etanercept or substitution with etanercept should be considered as treatment options for patients not adequately responding to sulfasalazine.</p>
</sec>
</div>
</front>
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