author_facet Palsson, Olafur
Love, Thorvardur Jon
Gunnarsdottir, Anna Ingibjorg
Gunnarsson, Petur Sigurdur
Runarsdottir, Eydis Erla
Krogh, Niels Steen
Gudbjornsson, Bjorn
Palsson, Olafur
Love, Thorvardur Jon
Gunnarsdottir, Anna Ingibjorg
Gunnarsson, Petur Sigurdur
Runarsdottir, Eydis Erla
Krogh, Niels Steen
Gudbjornsson, Bjorn
author Palsson, Olafur
Love, Thorvardur Jon
Gunnarsdottir, Anna Ingibjorg
Gunnarsson, Petur Sigurdur
Runarsdottir, Eydis Erla
Krogh, Niels Steen
Gudbjornsson, Bjorn
spellingShingle Palsson, Olafur
Love, Thorvardur Jon
Gunnarsdottir, Anna Ingibjorg
Gunnarsson, Petur Sigurdur
Runarsdottir, Eydis Erla
Krogh, Niels Steen
Gudbjornsson, Bjorn
RMD Open
Patients with psoriatic arthritis who are not eligible for randomised controlled trials for TNF inhibitors have treatment response and drug survival similar to those who are eligible
Immunology
Immunology and Allergy
Rheumatology
author_sort palsson, olafur
spelling Palsson, Olafur Love, Thorvardur Jon Gunnarsdottir, Anna Ingibjorg Gunnarsson, Petur Sigurdur Runarsdottir, Eydis Erla Krogh, Niels Steen Gudbjornsson, Bjorn 2056-5933 BMJ Immunology Immunology and Allergy Rheumatology http://dx.doi.org/10.1136/rmdopen-2019-000984 <jats:sec><jats:title>Objectives</jats:title><jats:p>To determine in a retrospective cohort whether patients with psoriatic arthritis (PsA) who would not have fulfilled the inclusion criteria for randomised controlled trials (RCTs) for the TNF inhibitor (TNFi) chosen for their treatment (excl) have similar benefits and drug survival as those patients who would have (incl).</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>All patients with rheumatic disorders who are treated with biological disease-modifying antirheumatic drugs in Iceland are registered in ICEBIO. On 1 February 2016, 329 individuals with PsA were registered in ICEBIO, of whom 231 had data available for their first start of TNFi and could be evaluated according to the inclusion criteria of the respective RCTs. Disease activity was collected at baseline using Visual Analogue Scale (pain, fatigue and global (patient and physician) assessments), swollen joint count (SJC) and tender joint count (TJC), Disease Activity Score 28-joint count C reactive protein (DAS28-CRP) and Health Assessment Questionnaire (HAQ). Treatment response was measured at 6 and 18 months according to American College of Rheumatology response criteria, DAS28-CRP and Disease Activity Score in Psoriatic Arthritis for 28 joints. Drug survival rate was also analysed.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>The demographics of these two groups were similar at baseline, although the incl group had higher SJC (5.5 vs 3.8) and subsequently higher DAS28-CRP (4.6 vs 4.2). While a larger change in disease activity was observed in the incl group with respect to HAQ and SJC, both groups had similar disease activity at follow-up. Drug survival was similar in both groups.</jats:p></jats:sec><jats:sec><jats:title>Conclusions</jats:title><jats:p>Patients with PsA who would not have fulfilled the inclusion criteria in RCTs reach similar disease activity scores at follow-up of 6 and 18 months and have similar drug survival as those patients who would have been included in RCTs.</jats:p></jats:sec> Patients with psoriatic arthritis who are not eligible for randomised controlled trials for TNF inhibitors have treatment response and drug survival similar to those who are eligible RMD Open
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publisher BMJ
recordtype ai
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title Patients with psoriatic arthritis who are not eligible for randomised controlled trials for TNF inhibitors have treatment response and drug survival similar to those who are eligible
title_unstemmed Patients with psoriatic arthritis who are not eligible for randomised controlled trials for TNF inhibitors have treatment response and drug survival similar to those who are eligible
title_full Patients with psoriatic arthritis who are not eligible for randomised controlled trials for TNF inhibitors have treatment response and drug survival similar to those who are eligible
title_fullStr Patients with psoriatic arthritis who are not eligible for randomised controlled trials for TNF inhibitors have treatment response and drug survival similar to those who are eligible
title_full_unstemmed Patients with psoriatic arthritis who are not eligible for randomised controlled trials for TNF inhibitors have treatment response and drug survival similar to those who are eligible
title_short Patients with psoriatic arthritis who are not eligible for randomised controlled trials for TNF inhibitors have treatment response and drug survival similar to those who are eligible
title_sort patients with psoriatic arthritis who are not eligible for randomised controlled trials for tnf inhibitors have treatment response and drug survival similar to those who are eligible
topic Immunology
Immunology and Allergy
Rheumatology
url http://dx.doi.org/10.1136/rmdopen-2019-000984
publishDate 2019
physical e000984
description <jats:sec><jats:title>Objectives</jats:title><jats:p>To determine in a retrospective cohort whether patients with psoriatic arthritis (PsA) who would not have fulfilled the inclusion criteria for randomised controlled trials (RCTs) for the TNF inhibitor (TNFi) chosen for their treatment (excl) have similar benefits and drug survival as those patients who would have (incl).</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>All patients with rheumatic disorders who are treated with biological disease-modifying antirheumatic drugs in Iceland are registered in ICEBIO. On 1 February 2016, 329 individuals with PsA were registered in ICEBIO, of whom 231 had data available for their first start of TNFi and could be evaluated according to the inclusion criteria of the respective RCTs. Disease activity was collected at baseline using Visual Analogue Scale (pain, fatigue and global (patient and physician) assessments), swollen joint count (SJC) and tender joint count (TJC), Disease Activity Score 28-joint count C reactive protein (DAS28-CRP) and Health Assessment Questionnaire (HAQ). Treatment response was measured at 6 and 18 months according to American College of Rheumatology response criteria, DAS28-CRP and Disease Activity Score in Psoriatic Arthritis for 28 joints. Drug survival rate was also analysed.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>The demographics of these two groups were similar at baseline, although the incl group had higher SJC (5.5 vs 3.8) and subsequently higher DAS28-CRP (4.6 vs 4.2). While a larger change in disease activity was observed in the incl group with respect to HAQ and SJC, both groups had similar disease activity at follow-up. Drug survival was similar in both groups.</jats:p></jats:sec><jats:sec><jats:title>Conclusions</jats:title><jats:p>Patients with PsA who would not have fulfilled the inclusion criteria in RCTs reach similar disease activity scores at follow-up of 6 and 18 months and have similar drug survival as those patients who would have been included in RCTs.</jats:p></jats:sec>
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author Palsson, Olafur, Love, Thorvardur Jon, Gunnarsdottir, Anna Ingibjorg, Gunnarsson, Petur Sigurdur, Runarsdottir, Eydis Erla, Krogh, Niels Steen, Gudbjornsson, Bjorn
author_facet Palsson, Olafur, Love, Thorvardur Jon, Gunnarsdottir, Anna Ingibjorg, Gunnarsson, Petur Sigurdur, Runarsdottir, Eydis Erla, Krogh, Niels Steen, Gudbjornsson, Bjorn, Palsson, Olafur, Love, Thorvardur Jon, Gunnarsdottir, Anna Ingibjorg, Gunnarsson, Petur Sigurdur, Runarsdottir, Eydis Erla, Krogh, Niels Steen, Gudbjornsson, Bjorn
author_sort palsson, olafur
container_issue 2
container_start_page 0
container_title RMD Open
container_volume 5
description <jats:sec><jats:title>Objectives</jats:title><jats:p>To determine in a retrospective cohort whether patients with psoriatic arthritis (PsA) who would not have fulfilled the inclusion criteria for randomised controlled trials (RCTs) for the TNF inhibitor (TNFi) chosen for their treatment (excl) have similar benefits and drug survival as those patients who would have (incl).</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>All patients with rheumatic disorders who are treated with biological disease-modifying antirheumatic drugs in Iceland are registered in ICEBIO. On 1 February 2016, 329 individuals with PsA were registered in ICEBIO, of whom 231 had data available for their first start of TNFi and could be evaluated according to the inclusion criteria of the respective RCTs. Disease activity was collected at baseline using Visual Analogue Scale (pain, fatigue and global (patient and physician) assessments), swollen joint count (SJC) and tender joint count (TJC), Disease Activity Score 28-joint count C reactive protein (DAS28-CRP) and Health Assessment Questionnaire (HAQ). Treatment response was measured at 6 and 18 months according to American College of Rheumatology response criteria, DAS28-CRP and Disease Activity Score in Psoriatic Arthritis for 28 joints. Drug survival rate was also analysed.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>The demographics of these two groups were similar at baseline, although the incl group had higher SJC (5.5 vs 3.8) and subsequently higher DAS28-CRP (4.6 vs 4.2). While a larger change in disease activity was observed in the incl group with respect to HAQ and SJC, both groups had similar disease activity at follow-up. Drug survival was similar in both groups.</jats:p></jats:sec><jats:sec><jats:title>Conclusions</jats:title><jats:p>Patients with PsA who would not have fulfilled the inclusion criteria in RCTs reach similar disease activity scores at follow-up of 6 and 18 months and have similar drug survival as those patients who would have been included in RCTs.</jats:p></jats:sec>
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spelling Palsson, Olafur Love, Thorvardur Jon Gunnarsdottir, Anna Ingibjorg Gunnarsson, Petur Sigurdur Runarsdottir, Eydis Erla Krogh, Niels Steen Gudbjornsson, Bjorn 2056-5933 BMJ Immunology Immunology and Allergy Rheumatology http://dx.doi.org/10.1136/rmdopen-2019-000984 <jats:sec><jats:title>Objectives</jats:title><jats:p>To determine in a retrospective cohort whether patients with psoriatic arthritis (PsA) who would not have fulfilled the inclusion criteria for randomised controlled trials (RCTs) for the TNF inhibitor (TNFi) chosen for their treatment (excl) have similar benefits and drug survival as those patients who would have (incl).</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>All patients with rheumatic disorders who are treated with biological disease-modifying antirheumatic drugs in Iceland are registered in ICEBIO. On 1 February 2016, 329 individuals with PsA were registered in ICEBIO, of whom 231 had data available for their first start of TNFi and could be evaluated according to the inclusion criteria of the respective RCTs. Disease activity was collected at baseline using Visual Analogue Scale (pain, fatigue and global (patient and physician) assessments), swollen joint count (SJC) and tender joint count (TJC), Disease Activity Score 28-joint count C reactive protein (DAS28-CRP) and Health Assessment Questionnaire (HAQ). Treatment response was measured at 6 and 18 months according to American College of Rheumatology response criteria, DAS28-CRP and Disease Activity Score in Psoriatic Arthritis for 28 joints. Drug survival rate was also analysed.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>The demographics of these two groups were similar at baseline, although the incl group had higher SJC (5.5 vs 3.8) and subsequently higher DAS28-CRP (4.6 vs 4.2). While a larger change in disease activity was observed in the incl group with respect to HAQ and SJC, both groups had similar disease activity at follow-up. Drug survival was similar in both groups.</jats:p></jats:sec><jats:sec><jats:title>Conclusions</jats:title><jats:p>Patients with PsA who would not have fulfilled the inclusion criteria in RCTs reach similar disease activity scores at follow-up of 6 and 18 months and have similar drug survival as those patients who would have been included in RCTs.</jats:p></jats:sec> Patients with psoriatic arthritis who are not eligible for randomised controlled trials for TNF inhibitors have treatment response and drug survival similar to those who are eligible RMD Open
spellingShingle Palsson, Olafur, Love, Thorvardur Jon, Gunnarsdottir, Anna Ingibjorg, Gunnarsson, Petur Sigurdur, Runarsdottir, Eydis Erla, Krogh, Niels Steen, Gudbjornsson, Bjorn, RMD Open, Patients with psoriatic arthritis who are not eligible for randomised controlled trials for TNF inhibitors have treatment response and drug survival similar to those who are eligible, Immunology, Immunology and Allergy, Rheumatology
title Patients with psoriatic arthritis who are not eligible for randomised controlled trials for TNF inhibitors have treatment response and drug survival similar to those who are eligible
title_full Patients with psoriatic arthritis who are not eligible for randomised controlled trials for TNF inhibitors have treatment response and drug survival similar to those who are eligible
title_fullStr Patients with psoriatic arthritis who are not eligible for randomised controlled trials for TNF inhibitors have treatment response and drug survival similar to those who are eligible
title_full_unstemmed Patients with psoriatic arthritis who are not eligible for randomised controlled trials for TNF inhibitors have treatment response and drug survival similar to those who are eligible
title_short Patients with psoriatic arthritis who are not eligible for randomised controlled trials for TNF inhibitors have treatment response and drug survival similar to those who are eligible
title_sort patients with psoriatic arthritis who are not eligible for randomised controlled trials for tnf inhibitors have treatment response and drug survival similar to those who are eligible
title_unstemmed Patients with psoriatic arthritis who are not eligible for randomised controlled trials for TNF inhibitors have treatment response and drug survival similar to those who are eligible
topic Immunology, Immunology and Allergy, Rheumatology
url http://dx.doi.org/10.1136/rmdopen-2019-000984