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                  <mods:namePart>Taxonera, Carlos</mods:namePart>
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                  <mods:namePart>García-Brenes, Miguel A</mods:namePart>
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                  <mods:namePart>Zapater, Raúl</mods:namePart>
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                  <mods:namePart>Alba, Cristina</mods:namePart>
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               <mods:identifier type="citation">Taxonera C, García-Brenes MA, Machín M, Olivares D, López-García ON, Zapater R, Alba C. Real-World Effectiveness and Safety of Upadacitinib in Patients with Ulcerative Colitis: A Systematic Review and Meta-Analysis. J Clin Med. 2025 Mar 25;14(7):2232.</mods:identifier>
               <mods:identifier type="doi">10.3390/jcm14072232</mods:identifier>
               <mods:identifier type="issn">2077-0383</mods:identifier>
               <mods:identifier type="journal">ournal of clinical medicine</mods:identifier>
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               <mods:abstract>Background/Objectives: Evidence is needed on the real-world outcomes of upadacitinib in patients with ulcerative colitis. This systematic review and meta-analysis evaluated the real-world effectiveness of upadacitinib for active UC. Methods: The primary outcome was clinical remission evaluated at week 8. Secondary outcomes included response, steroid-free remission, biochemical remission, colectomy, and safety. A random-effects meta-analysis model was used to calculate the pooled effect sizes (percentages or incidence rates) of effectiveness and safety outcomes. Results: Twenty-four studies with 1388 patients were included. Ninety-four percent of patients had previously failed biologics or Janus kinase inhibitors (JAKi), including 53.2% with tofacitinib. Clinical remission at week 8 was achieved in 68.4% of patients (95% confidence interval 55.5-80.2). Clinical remission was achieved in 48.3%, 71.1%, and 64.6% of patients at weeks 2 to 6, 12 to 16, and 24 to 36, respectively. Response was achieved in 72.6%, 82.1%, and 78.7% of patients at weeks 2 to 6, week 8, and weeks 12 to 16, respectively. Steroid-free remission was achieved in 39% of patients at week 8. Upadacitinib results were unaffected by prior biologic or JAKi failure. Mean fecal calprotectin level decreased from 1485.0 µ/g at baseline to 454.8 µ/g post-treatment (p &lt; 0.01). The mean CRP level decreased from 12.3 mg/L at baseline to 4.4 mg/L post-treatment (p = 0.02). The incidence rates of colectomy, serious adverse events, and herpes zoster were 13.3, 2.3, and 1.7 per 100 patient-years, respectively. Conclusions: This meta-analysis confirms the effectiveness and safety of upadacitinib in a highly treatment-refractory population of UC patients.</mods:abstract>
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                  <mods:topic>Janus kinase</mods:topic>
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                  <mods:topic>Meta-analysis</mods:topic>
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                  <mods:topic>Real-world effectiveness</mods:topic>
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                  <mods:topic>Safety</mods:topic>
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                  <mods:topic>Ulcerative colitis</mods:topic>
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                  <mods:topic>Upadacitinib</mods:topic>
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                  <mods:title>Real-World Effectiveness and Safety of Upadacitinib in Patients with Ulcerative Colitis: A Systematic Review and Meta-Analysis</mods:title>
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