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Effects of switching between anti-TNF therapies on HAQ response in patients who do not respond to their first anti-TNF drug

Objectives. Small studies have shown an improvement in disease activity in patients with RA who have switched between anti-TNF therapies for reasons of inefficacy. However, it is not clear whether switching improves longer term outcomes, such as disability. This analysis compares changes in HAQ scor...

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Autores principales: Hyrich, K. L., Lunt, M., Dixon, W. G., Watson, K. D., Symmons, D. P. M.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2430221/
https://www.ncbi.nlm.nih.gov/pubmed/18420660
http://dx.doi.org/10.1093/rheumatology/ken127
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author Hyrich, K. L.
Lunt, M.
Dixon, W. G.
Watson, K. D.
Symmons, D. P. M.
author_facet Hyrich, K. L.
Lunt, M.
Dixon, W. G.
Watson, K. D.
Symmons, D. P. M.
author_sort Hyrich, K. L.
collection PubMed
description Objectives. Small studies have shown an improvement in disease activity in patients with RA who have switched between anti-TNF therapies for reasons of inefficacy. However, it is not clear whether switching improves longer term outcomes, such as disability. This analysis compares changes in HAQ scores 1 yr following lack of response to a first anti-TNF based on subsequent treatment during that year. Methods. Analysis was limited to RA patients with inefficacy to a first anti-TNF based on (i) clinician opinion and/or (ii) disease activity score in 28 joints and had an HAQ measured at time of non-response and 12 months later. Patients were classified into three groups based on treatment during the next 12 months: (i) continued anti-TNF despite non-response; (ii) stopped anti-TNF with no further biologics; and (iii) switched to a second anti-TNF. Mean improvement in HAQ was compared among the groups using multivariable linear regression models. Results. As of July 2006, 868 patients met the inclusion for this analysis. Four hundred and seventy-nine patients stopped anti-TNF of whom 331 switched to a second anti-TNF. Three hundred and eighty-nine continued treatment. Patients who continued and those who switched had improvements in HAQ over the 12 months, unlike patients who discontinued all biologic therapy. The best improvement was seen in those who switched [adjusted mean improvement in HAQ 0.15 (95% CI 0.26, 0.05)]. Conclusion. There is a significant improvement in HAQ in patients who switch to a second anti-TNF, providing an effective next choice of therapy for some patients who fail to respond to their first anti-TNF.
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spelling pubmed-24302212009-02-25 Effects of switching between anti-TNF therapies on HAQ response in patients who do not respond to their first anti-TNF drug Hyrich, K. L. Lunt, M. Dixon, W. G. Watson, K. D. Symmons, D. P. M. Rheumatology (Oxford) Clinical Objectives. Small studies have shown an improvement in disease activity in patients with RA who have switched between anti-TNF therapies for reasons of inefficacy. However, it is not clear whether switching improves longer term outcomes, such as disability. This analysis compares changes in HAQ scores 1 yr following lack of response to a first anti-TNF based on subsequent treatment during that year. Methods. Analysis was limited to RA patients with inefficacy to a first anti-TNF based on (i) clinician opinion and/or (ii) disease activity score in 28 joints and had an HAQ measured at time of non-response and 12 months later. Patients were classified into three groups based on treatment during the next 12 months: (i) continued anti-TNF despite non-response; (ii) stopped anti-TNF with no further biologics; and (iii) switched to a second anti-TNF. Mean improvement in HAQ was compared among the groups using multivariable linear regression models. Results. As of July 2006, 868 patients met the inclusion for this analysis. Four hundred and seventy-nine patients stopped anti-TNF of whom 331 switched to a second anti-TNF. Three hundred and eighty-nine continued treatment. Patients who continued and those who switched had improvements in HAQ over the 12 months, unlike patients who discontinued all biologic therapy. The best improvement was seen in those who switched [adjusted mean improvement in HAQ 0.15 (95% CI 0.26, 0.05)]. Conclusion. There is a significant improvement in HAQ in patients who switch to a second anti-TNF, providing an effective next choice of therapy for some patients who fail to respond to their first anti-TNF. Oxford University Press 2008-07 2008-04-17 /pmc/articles/PMC2430221/ /pubmed/18420660 http://dx.doi.org/10.1093/rheumatology/ken127 Text en © 2008 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical
Hyrich, K. L.
Lunt, M.
Dixon, W. G.
Watson, K. D.
Symmons, D. P. M.
Effects of switching between anti-TNF therapies on HAQ response in patients who do not respond to their first anti-TNF drug
title Effects of switching between anti-TNF therapies on HAQ response in patients who do not respond to their first anti-TNF drug
title_full Effects of switching between anti-TNF therapies on HAQ response in patients who do not respond to their first anti-TNF drug
title_fullStr Effects of switching between anti-TNF therapies on HAQ response in patients who do not respond to their first anti-TNF drug
title_full_unstemmed Effects of switching between anti-TNF therapies on HAQ response in patients who do not respond to their first anti-TNF drug
title_short Effects of switching between anti-TNF therapies on HAQ response in patients who do not respond to their first anti-TNF drug
title_sort effects of switching between anti-tnf therapies on haq response in patients who do not respond to their first anti-tnf drug
topic Clinical
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2430221/
https://www.ncbi.nlm.nih.gov/pubmed/18420660
http://dx.doi.org/10.1093/rheumatology/ken127
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