<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>36(1)</volume><submitter>Meijboom RW</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Transitioning patients from an originator to a corresponding biosimilar has been extensively studied in both randomized controlled trials and observational studies. Although transitioning is considered well-tolerated, with no negative impacts on efficacy and/or safety, 2.6-25.8% of patients restart treatment with the originator (retransitioning). Retransitioning to the originator can be considered an indication of biosimilar treatment failure or dissatisfaction with biosimilar treatment. Increasing our knowledge of patients who retransition might help to reduce the number of patients retransitioning.&lt;h4>Objective&lt;/h4>Our objective was to estimate the cumulative incidence of patients who retransitioned from a tumor necrosis factor (TNF)-α inhibitor biosimilar to originato</pubmed_abstract><journal>BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy</journal><pagination>27-39</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8847209</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Patients Retransitioning from Biosimilar TNFα Inhibitor to the Corresponding Originator After Initial Transitioning to the Biosimilar: A Systematic Review.</pubmed_title><pmcid>PMC8847209</pmcid><pubmed_authors>Egberts TCG</pubmed_authors><pubmed_authors>Gardarsdottir H</pubmed_authors><pubmed_authors>Giezen TJ</pubmed_authors><pubmed_authors>Meijboom RW</pubmed_authors></additional><is_claimable>false</is_claimable><name>Patients Retransitioning from Biosimilar TNFα Inhibitor to the Corresponding Originator After Initial Transitioning to the Biosimilar: A Systematic Review.</name><description>&lt;h4>Background&lt;/h4>Transitioning patients from an originator to a corresponding biosimilar has been extensively studied in both randomized controlled trials and observational studies. Although transitioning is considered well-tolerated, with no negative impacts on efficacy and/or safety, 2.6-25.8% of patients restart treatment with the originator (retransitioning). Retransitioning to the originator can be considered an indication of biosimilar treatment failure or dissatisfaction with biosimilar treatment. Increasing our knowledge of patients who retransition might help to reduce the number of patients retransitioning.&lt;h4>Objective&lt;/h4>Our objective was to estimate the cumulative incidence of patients who retransitioned from a tumor necrosis factor (TNF)-α inhibitor biosimilar to originato</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jan</publication><modification>2025-04-05T11:07:19.75Z</modification><creation>2025-04-05T11:07:19.75Z</creation></dates><accession>S-EPMC8847209</accession><cross_references><pubmed>34870802</pubmed><doi>10.1007/s40259-021-00508-4</doi></cross_references></HashMap>