<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Taylor PC</submitter><funding>AbbVie</funding><pubmed_abstract>&lt;h4>Introduction&lt;/h4>The aim of this work is to compare real-world outcomes of patients with rheumatoid arthritis (RA) receiving adalimumab (ADA) bio-originator (non-switchers) to those who had switched from ADA bio-originator to an ADA biosimilar (switchers) on the basis of the hypothesis that these outcomes would differ.&lt;h4>Methods&lt;/h4>Data were drawn from the Adelphi RA Disease Specific Programme™, a point-in-time survey of physicians and their patients in Europe (France, Germany, Italy, Spain, UK) in 2020. Physicians completed a questionnaire for their next ten adult patients with RA, followed by four additional patients who had switched from ADA bio-originator to an ADA biosimilar (switchers). Physician- and patient-reported outcomes (PROs) for switchers and non-switchers were compared by propensity score matching.&lt;h4>Results&lt;/h4>Three hundred and three rheumatologists provided data for 160 non-switchers and 225 switchers, 140 patients provided data; 51 non-switchers, 89 switchers. According to physician-reported disease activity, non-switchers were more likely to improve on their current ADA treatment than switchers (68%, n = 108 vs. 26%, n = 59 p &lt; 0.001) and less likely to worsen (1%, n = 2 vs. 9%, n = 20; p &lt; 0.01). Physician-reported patient adherence was significantly lower amongst switchers versus non-switchers (0.66 vs. 0.78, respectively; p = 0.04). More non-switchers than switchers were reported by their physicians to be consistent in taking their RA medicine (p &lt; 0.001). Compared with non-switchers, PRO measures indicated quality of life was worse (EQ-5D Visual Analogue Scale: 62.9 vs. 71.9; p &lt; 0.001) and activity impairment was greater (Work Productivity Activity Index: 31.0 vs. 24.4; p = 0.02) for switchers, with trends for poorer health status and greater pain.&lt;h4>Conclusions&lt;/h4>Non-medical switching in RA treatment may lead to unforeseen outcomes that should be considered by health decision-makers.</pubmed_abstract><journal>Rheumatology and therapy</journal><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9834672</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Outcomes Following Adalimumab Bio-originator to Biosimilar Switch-A Comparison Using Real-world Patient- and Physician-Reported Data in European Countries.</pubmed_title><pmcid>PMC9834672</pmcid><pubmed_authors>Taylor PC</pubmed_authors><pubmed_authors>Faccin F</pubmed_authors><pubmed_authors>Clark R</pubmed_authors><pubmed_authors>Gonzalez YS</pubmed_authors><pubmed_authors>Howell O</pubmed_authors></additional><is_claimable>false</is_claimable><name>Outcomes Following Adalimumab Bio-originator to Biosimilar Switch-A Comparison Using Real-world Patient- and Physician-Reported Data in European Countries.</name><description>&lt;h4>Introduction&lt;/h4>The aim of this work is to compare real-world outcomes of patients with rheumatoid arthritis (RA) receiving adalimumab (ADA) bio-originator (non-switchers) to those who had switched from ADA bio-originator to an ADA biosimilar (switchers) on the basis of the hypothesis that these outcomes would differ.&lt;h4>Methods&lt;/h4>Data were drawn from the Adelphi RA Disease Specific Programme™, a point-in-time survey of physicians and their patients in Europe (France, Germany, Italy, Spain, UK) in 2020. Physicians completed a questionnaire for their next ten adult patients with RA, followed by four additional patients who had switched from ADA bio-originator to an ADA biosimilar (switchers). Physician- and patient-reported outcomes (PROs) for switchers and non-switchers were compared by propensity score matching.&lt;h4>Results&lt;/h4>Three hundred and three rheumatologists provided data for 160 non-switchers and 225 switchers, 140 patients provided data; 51 non-switchers, 89 switchers. According to physician-reported disease activity, non-switchers were more likely to improve on their current ADA treatment than switchers (68%, n = 108 vs. 26%, n = 59 p &lt; 0.001) and less likely to worsen (1%, n = 2 vs. 9%, n = 20; p &lt; 0.01). Physician-reported patient adherence was significantly lower amongst switchers versus non-switchers (0.66 vs. 0.78, respectively; p = 0.04). More non-switchers than switchers were reported by their physicians to be consistent in taking their RA medicine (p &lt; 0.001). Compared with non-switchers, PRO measures indicated quality of life was worse (EQ-5D Visual Analogue Scale: 62.9 vs. 71.9; p &lt; 0.001) and activity impairment was greater (Work Productivity Activity Index: 31.0 vs. 24.4; p = 0.02) for switchers, with trends for poorer health status and greater pain.&lt;h4>Conclusions&lt;/h4>Non-medical switching in RA treatment may lead to unforeseen outcomes that should be considered by health decision-makers.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2024-11-12T02:31:15.699Z</modification><creation>2024-11-12T02:31:15.699Z</creation></dates><accession>S-EPMC9834672</accession><cross_references><pubmed>36631636</pubmed><doi>10.1007/s40744-022-00526-w</doi></cross_references></HashMap>