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The impact of four dynamic, goal-steered treatment strategies on the 5-year outcomes of rheumatoid arthritis patients in the BeSt study

Identifieur interne : 002976 ( Istex/Corpus ); précédent : 002975; suivant : 002977

The impact of four dynamic, goal-steered treatment strategies on the 5-year outcomes of rheumatoid arthritis patients in the BeSt study

Auteurs : Naomi B. Klarenbeek ; Melek Güler-Yüksel ; Sjoerd M. Van Der Kooij ; K Huub Han ; H Karel Ronday ; Pit J S M. Kerstens ; Patrick E H. Seys ; Tom W J. Huizinga ; Ben A C. Dijkmans ; Cornelia F. Allaart

Source :

RBID : ISTEX:13B207CBF804CAEE46AE02E9D5AF73B776C4F230

English descriptors

Abstract

Objective To compare clinical and radiological outcomes of four dynamic treatment strategies in recent-onset rheumatoid arthritis (RA) after 5 years follow-up. Methods 508 patients with recent-onset RA were randomly assigned into four treatment strategies: sequential monotherapy; step-up combination therapy; initial combination with prednisone; initial combination with infliximab. Treatment adjustments were made based on 3-monthly disease activity score (DAS) measurements (if DAS >2.4 next treatment step; if DAS ≤2.4 during ≥6 months taper to maintenance dose; if DAS <1.6 during ≥6 months stop antirheumatic treatment). Primary and secondary outcomes were functional ability, joint damage progression, health-related quality of life and (drug-free) remission percentages. Results After 5 years, 48% of patients were in clinical remission (DAS <1.6) and 14% in drug-free remission, irrespective of initial treatment. After an earlier improvement in functional ability and quality of life with initial combination therapy, from 1 year onwards clinical outcomes were comparable across the groups and stable during 5 years. The initial combination groups showed less joint damage in year 1. In years 2–5 annual progression was comparable across the groups. After 5 years, initial combination therapy resulted in significantly less joint damage progression, reflecting the earlier clinical response. Conclusion Irrespective of initial treatment, an impressive improvement in clinical and radiological outcomes of RA patients can be achieved with dynamic treatment aimed at reducing disease activity, leading to 48% remission, 14% drug-free remission and sustained functional improvement. Starting with combination therapy resulted in earlier clinical improvement and less joint damage without more toxicity.

Url:
DOI: 10.1136/ard.2010.141234

Links to Exploration step

ISTEX:13B207CBF804CAEE46AE02E9D5AF73B776C4F230

Le document en format XML

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<div type="abstract">Objective To compare clinical and radiological outcomes of four dynamic treatment strategies in recent-onset rheumatoid arthritis (RA) after 5 years follow-up. Methods 508 patients with recent-onset RA were randomly assigned into four treatment strategies: sequential monotherapy; step-up combination therapy; initial combination with prednisone; initial combination with infliximab. Treatment adjustments were made based on 3-monthly disease activity score (DAS) measurements (if DAS >2.4 next treatment step; if DAS ≤2.4 during ≥6 months taper to maintenance dose; if DAS <1.6 during ≥6 months stop antirheumatic treatment). Primary and secondary outcomes were functional ability, joint damage progression, health-related quality of life and (drug-free) remission percentages. Results After 5 years, 48% of patients were in clinical remission (DAS <1.6) and 14% in drug-free remission, irrespective of initial treatment. After an earlier improvement in functional ability and quality of life with initial combination therapy, from 1 year onwards clinical outcomes were comparable across the groups and stable during 5 years. The initial combination groups showed less joint damage in year 1. In years 2–5 annual progression was comparable across the groups. After 5 years, initial combination therapy resulted in significantly less joint damage progression, reflecting the earlier clinical response. Conclusion Irrespective of initial treatment, an impressive improvement in clinical and radiological outcomes of RA patients can be achieved with dynamic treatment aimed at reducing disease activity, leading to 48% remission, 14% drug-free remission and sustained functional improvement. Starting with combination therapy resulted in earlier clinical improvement and less joint damage without more toxicity.</div>
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<abstract>Objective To compare clinical and radiological outcomes of four dynamic treatment strategies in recent-onset rheumatoid arthritis (RA) after 5 years follow-up. Methods 508 patients with recent-onset RA were randomly assigned into four treatment strategies: sequential monotherapy; step-up combination therapy; initial combination with prednisone; initial combination with infliximab. Treatment adjustments were made based on 3-monthly disease activity score (DAS) measurements (if DAS >2.4 next treatment step; if DAS ≤2.4 during ≥6 months taper to maintenance dose; if DAS >1.6 during ≥6 months stop antirheumatic treatment). Primary and secondary outcomes were functional ability, joint damage progression, health-related quality of life and (drug-free) remission percentages. Results After 5 years, 48% of patients were in clinical remission (DAS >1.6) and 14% in drug-free remission, irrespective of initial treatment. After an earlier improvement in functional ability and quality of life with initial combination therapy, from 1 year onwards clinical outcomes were comparable across the groups and stable during 5 years. The initial combination groups showed less joint damage in year 1. In years 2–5 annual progression was comparable across the groups. After 5 years, initial combination therapy resulted in significantly less joint damage progression, reflecting the earlier clinical response. Conclusion Irrespective of initial treatment, an impressive improvement in clinical and radiological outcomes of RA patients can be achieved with dynamic treatment aimed at reducing disease activity, leading to 48% remission, 14% drug-free remission and sustained functional improvement. Starting with combination therapy resulted in earlier clinical improvement and less joint damage without more toxicity.</abstract>
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<p>Objective To compare clinical and radiological outcomes of four dynamic treatment strategies in recent-onset rheumatoid arthritis (RA) after 5 years follow-up. Methods 508 patients with recent-onset RA were randomly assigned into four treatment strategies: sequential monotherapy; step-up combination therapy; initial combination with prednisone; initial combination with infliximab. Treatment adjustments were made based on 3-monthly disease activity score (DAS) measurements (if DAS >2.4 next treatment step; if DAS ≤2.4 during ≥6 months taper to maintenance dose; if DAS <1.6 during ≥6 months stop antirheumatic treatment). Primary and secondary outcomes were functional ability, joint damage progression, health-related quality of life and (drug-free) remission percentages. Results After 5 years, 48% of patients were in clinical remission (DAS <1.6) and 14% in drug-free remission, irrespective of initial treatment. After an earlier improvement in functional ability and quality of life with initial combination therapy, from 1 year onwards clinical outcomes were comparable across the groups and stable during 5 years. The initial combination groups showed less joint damage in year 1. In years 2–5 annual progression was comparable across the groups. After 5 years, initial combination therapy resulted in significantly less joint damage progression, reflecting the earlier clinical response. Conclusion Irrespective of initial treatment, an impressive improvement in clinical and radiological outcomes of RA patients can be achieved with dynamic treatment aimed at reducing disease activity, leading to 48% remission, 14% drug-free remission and sustained functional improvement. Starting with combination therapy resulted in earlier clinical improvement and less joint damage without more toxicity.</p>
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<article-title>The impact of four dynamic, goal-steered treatment strategies on the 5-year outcomes of rheumatoid arthritis patients in the BeSt study</article-title>
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<contrib contrib-type="author">
<name>
<surname>Klarenbeek</surname>
<given-names>Naomi B</given-names>
</name>
<xref ref-type="aff" rid="A1">1</xref>
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<name>
<surname>Güler-Yüksel</surname>
<given-names>Melek</given-names>
</name>
<xref ref-type="aff" rid="A1">1</xref>
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<name>
<surname>van der Kooij</surname>
<given-names>Sjoerd M</given-names>
</name>
<xref ref-type="aff" rid="A1">1</xref>
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<name>
<surname>Han</surname>
<given-names>K Huub</given-names>
</name>
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<name>
<surname>Ronday</surname>
<given-names>H Karel</given-names>
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<name>
<surname>Kerstens</surname>
<given-names>Pit J S M</given-names>
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<xref ref-type="aff" rid="A4">4</xref>
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<name>
<surname>Seys</surname>
<given-names>Patrick E H</given-names>
</name>
<xref ref-type="aff" rid="A5">5</xref>
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<name>
<surname>Huizinga</surname>
<given-names>Tom W J</given-names>
</name>
<xref ref-type="aff" rid="A1">1</xref>
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<name>
<surname>Dijkmans</surname>
<given-names>Ben A C</given-names>
</name>
<xref ref-type="aff" rid="A4">4</xref>
<xref ref-type="aff" rid="A6">6</xref>
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<name>
<surname>Allaart</surname>
<given-names>Cornelia F</given-names>
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<aff id="A1">
<label>1</label>
Department of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands</aff>
<aff id="A2">
<label>2</label>
Department of Rheumatology, Maasstad Hospital, Rotterdam, The Netherlands</aff>
<aff id="A3">
<label>3</label>
Department of Rheumatology, Haga Hospital, The Hague, The Netherlands</aff>
<aff id="A4">
<label>4</label>
Department of Rheumatology, Jan van Breemen Institute, Amsterdam, The Netherlands</aff>
<aff id="A5">
<label>5</label>
Department of Rheumatology, Franciscus Hospital, Roosendaal, The Netherlands</aff>
<aff id="A6">
<label>6</label>
Department of Rheumatology, VU Medical Center, Amsterdam, The Netherlands</aff>
<author-notes>
<corresp>
<label>Correspondence to</label>
Dr N B Klarenbeek, Department of Rheumatology, C-01-R, Leiden University Medical Center, PO Box 9600, 2300 RC Leiden, The Netherlands;
<email xlink:type="simple">n.b.klarenbeek@lumc.nl</email>
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<title>Objective</title>
<p>To compare clinical and radiological outcomes of four dynamic treatment strategies in recent-onset rheumatoid arthritis (RA) after 5 years follow-up.</p>
</sec>
<sec>
<title>Methods</title>
<p>508 patients with recent-onset RA were randomly assigned into four treatment strategies: sequential monotherapy; step-up combination therapy; initial combination with prednisone; initial combination with infliximab. Treatment adjustments were made based on 3-monthly disease activity score (DAS) measurements (if DAS >2.4 next treatment step; if DAS ≤2.4 during ≥6 months taper to maintenance dose; if DAS <1.6 during ≥6 months stop antirheumatic treatment). Primary and secondary outcomes were functional ability, joint damage progression, health-related quality of life and (drug-free) remission percentages.</p>
</sec>
<sec>
<title>Results</title>
<p>After 5 years, 48% of patients were in clinical remission (DAS <1.6) and 14% in drug-free remission, irrespective of initial treatment. After an earlier improvement in functional ability and quality of life with initial combination therapy, from 1 year onwards clinical outcomes were comparable across the groups and stable during 5 years. The initial combination groups showed less joint damage in year 1. In years 2–5 annual progression was comparable across the groups. After 5 years, initial combination therapy resulted in significantly less joint damage progression, reflecting the earlier clinical response.</p>
</sec>
<sec>
<title>Conclusion</title>
<p>Irrespective of initial treatment, an impressive improvement in clinical and radiological outcomes of RA patients can be achieved with dynamic treatment aimed at reducing disease activity, leading to 48% remission, 14% drug-free remission and sustained functional improvement. Starting with combination therapy resulted in earlier clinical improvement and less joint damage without more toxicity.</p>
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<affiliation>Department of Rheumatology, Maasstad Hospital, Rotterdam, The Netherlands</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">H Karel</namePart>
<namePart type="family">Ronday</namePart>
<affiliation>Department of Rheumatology, Haga Hospital, The Hague, The Netherlands</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Pit J S M</namePart>
<namePart type="family">Kerstens</namePart>
<affiliation>Department of Rheumatology, Jan van Breemen Institute, Amsterdam, The Netherlands</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Patrick E H</namePart>
<namePart type="family">Seys</namePart>
<affiliation>Department of Rheumatology, Franciscus Hospital, Roosendaal, The Netherlands</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Tom W J</namePart>
<namePart type="family">Huizinga</namePart>
<affiliation>Department of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Ben A C</namePart>
<namePart type="family">Dijkmans</namePart>
<affiliation>Department of Rheumatology, Jan van Breemen Institute, Amsterdam, The Netherlands</affiliation>
<affiliation>Department of Rheumatology, VU Medical Center, Amsterdam, The Netherlands</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Cornelia F</namePart>
<namePart type="family">Allaart</namePart>
<affiliation>Department of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands</affiliation>
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<publisher>BMJ Publishing Group Ltd and European League Against Rheumatism</publisher>
<dateIssued encoding="w3cdtf">2011-06</dateIssued>
<dateCreated encoding="w3cdtf">2011-03-17</dateCreated>
<copyrightDate encoding="w3cdtf">2011</copyrightDate>
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<languageTerm type="code" authority="iso639-2b">eng</languageTerm>
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<abstract>Objective To compare clinical and radiological outcomes of four dynamic treatment strategies in recent-onset rheumatoid arthritis (RA) after 5 years follow-up. Methods 508 patients with recent-onset RA were randomly assigned into four treatment strategies: sequential monotherapy; step-up combination therapy; initial combination with prednisone; initial combination with infliximab. Treatment adjustments were made based on 3-monthly disease activity score (DAS) measurements (if DAS >2.4 next treatment step; if DAS ≤2.4 during ≥6 months taper to maintenance dose; if DAS <1.6 during ≥6 months stop antirheumatic treatment). Primary and secondary outcomes were functional ability, joint damage progression, health-related quality of life and (drug-free) remission percentages. Results After 5 years, 48% of patients were in clinical remission (DAS <1.6) and 14% in drug-free remission, irrespective of initial treatment. After an earlier improvement in functional ability and quality of life with initial combination therapy, from 1 year onwards clinical outcomes were comparable across the groups and stable during 5 years. The initial combination groups showed less joint damage in year 1. In years 2–5 annual progression was comparable across the groups. After 5 years, initial combination therapy resulted in significantly less joint damage progression, reflecting the earlier clinical response. Conclusion Irrespective of initial treatment, an impressive improvement in clinical and radiological outcomes of RA patients can be achieved with dynamic treatment aimed at reducing disease activity, leading to 48% remission, 14% drug-free remission and sustained functional improvement. Starting with combination therapy resulted in earlier clinical improvement and less joint damage without more toxicity.</abstract>
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<title>Annals of the Rheumatic Diseases</title>
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<title>Ann Rheum Dis</title>
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<identifier type="ISSN">0003-4967</identifier>
<identifier type="eISSN">1468-2060</identifier>
<identifier type="PublisherID">ard</identifier>
<identifier type="PublisherID-hwp">annrheumdis</identifier>
<identifier type="PublisherID-nlm-ta">Ann Rheum Dis</identifier>
<part>
<date>2011</date>
<detail type="volume">
<caption>vol.</caption>
<number>70</number>
</detail>
<detail type="issue">
<caption>no.</caption>
<number>6</number>
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<extent unit="pages">
<start>1039</start>
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<identifier type="istex">13B207CBF804CAEE46AE02E9D5AF73B776C4F230</identifier>
<identifier type="ark">ark:/67375/NVC-2ZWQGB8D-T</identifier>
<identifier type="DOI">10.1136/ard.2010.141234</identifier>
<identifier type="href">annrheumdis-70-1039.pdf</identifier>
<identifier type="ArticleID">annrheumdis141234</identifier>
<identifier type="PMID">21415052</identifier>
<identifier type="local">annrheumdis;70/6/1039</identifier>
<accessCondition type="use and reproduction" contentType="copyright">Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</accessCondition>
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<recordOrigin>Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</recordOrigin>
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