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Experience with Tofacitinib in Patients with Ulcerative Colitis: Data from a United States Claims Database

BACKGROUND: Tofacitinib is an oral small molecule Janus kinase inhibitor for the treatment of ulcerative colitis (UC). AIMS: To evaluate real-world data in US patients with UC receiving tofacitinib. METHODS: Characteristics and outcomes of patients with UC initiating tofacitinib between 2018 and 201...

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Autores principales: Chiorean, Michael, Ha, Christina, Hur, Peter, Sharma, Puza P., Gruben, David, Khan, Nabeel H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10516786/
https://www.ncbi.nlm.nih.gov/pubmed/37639057
http://dx.doi.org/10.1007/s10620-023-08063-4
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author Chiorean, Michael
Ha, Christina
Hur, Peter
Sharma, Puza P.
Gruben, David
Khan, Nabeel H.
author_facet Chiorean, Michael
Ha, Christina
Hur, Peter
Sharma, Puza P.
Gruben, David
Khan, Nabeel H.
author_sort Chiorean, Michael
collection PubMed
description BACKGROUND: Tofacitinib is an oral small molecule Janus kinase inhibitor for the treatment of ulcerative colitis (UC). AIMS: To evaluate real-world data in US patients with UC receiving tofacitinib. METHODS: Characteristics and outcomes of patients with UC initiating tofacitinib between 2018 and 2019 were assessed using data from the IBM® MarketScan® claims database. The index date was the first tofacitinib claim; pre- and post-index periods were 12 months. Outcomes included tofacitinib adherence/persistence, oral corticosteroid (OCS) use, and healthcare resource utilization (HCRU) and costs. RESULTS: Of 276 patients with UC who initiated tofacitinib, 68 (24.6%) were bio-naïve, and 208 (75.4%) bio-experienced. At month 12, overall median tofacitinib adherence (proportion of days covered) was 0.82 (mean 0.68); 43.8% of patients discontinued tofacitinib (90-day gap). Of patients receiving OCS during the post-index 16-week tapering period, 40.4% discontinued OCS up to 12 months post-index. OCS use decreased in patients continuing tofacitinib versus those discontinuing tofacitinib (29.7% vs 59.5%, respectively). Reductions in all-cause and UC-related outpatient visits were observed for bio-naïve (− 1.34 and − 0.88, respectively) and bio-experienced (− 4.72 and − 5.16, respectively) patients, post-index. Decreased UC-related costs per year were observed for bio-experienced patients (difference in post-index vs pre-index, − US$12,448; driven by changes in pharmacy costs), but not for bio-naïve patients (US$47,152). CONCLUSIONS: In this real-world analysis in a mostly bio-experienced population, the majority of US patients with UC initiating tofacitinib remained on therapy at 12 months, and OCS use was reduced with tofacitinib treatment. HCRU (all patients) and UC-related costs were reduced in bio-experienced patients. GRAPHICAL ABSTRACT: The majority of patients with ulcerative colitis starting tofacitinib in this real-world study continued therapy at 12 months; there was a reduction in the use of steroids, and a decrease in healthcare resournce utilization and costs. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10620-023-08063-4.
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spelling pubmed-105167862023-09-24 Experience with Tofacitinib in Patients with Ulcerative Colitis: Data from a United States Claims Database Chiorean, Michael Ha, Christina Hur, Peter Sharma, Puza P. Gruben, David Khan, Nabeel H. Dig Dis Sci Original Article BACKGROUND: Tofacitinib is an oral small molecule Janus kinase inhibitor for the treatment of ulcerative colitis (UC). AIMS: To evaluate real-world data in US patients with UC receiving tofacitinib. METHODS: Characteristics and outcomes of patients with UC initiating tofacitinib between 2018 and 2019 were assessed using data from the IBM® MarketScan® claims database. The index date was the first tofacitinib claim; pre- and post-index periods were 12 months. Outcomes included tofacitinib adherence/persistence, oral corticosteroid (OCS) use, and healthcare resource utilization (HCRU) and costs. RESULTS: Of 276 patients with UC who initiated tofacitinib, 68 (24.6%) were bio-naïve, and 208 (75.4%) bio-experienced. At month 12, overall median tofacitinib adherence (proportion of days covered) was 0.82 (mean 0.68); 43.8% of patients discontinued tofacitinib (90-day gap). Of patients receiving OCS during the post-index 16-week tapering period, 40.4% discontinued OCS up to 12 months post-index. OCS use decreased in patients continuing tofacitinib versus those discontinuing tofacitinib (29.7% vs 59.5%, respectively). Reductions in all-cause and UC-related outpatient visits were observed for bio-naïve (− 1.34 and − 0.88, respectively) and bio-experienced (− 4.72 and − 5.16, respectively) patients, post-index. Decreased UC-related costs per year were observed for bio-experienced patients (difference in post-index vs pre-index, − US$12,448; driven by changes in pharmacy costs), but not for bio-naïve patients (US$47,152). CONCLUSIONS: In this real-world analysis in a mostly bio-experienced population, the majority of US patients with UC initiating tofacitinib remained on therapy at 12 months, and OCS use was reduced with tofacitinib treatment. HCRU (all patients) and UC-related costs were reduced in bio-experienced patients. GRAPHICAL ABSTRACT: The majority of patients with ulcerative colitis starting tofacitinib in this real-world study continued therapy at 12 months; there was a reduction in the use of steroids, and a decrease in healthcare resournce utilization and costs. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10620-023-08063-4. Springer US 2023-08-28 2023 /pmc/articles/PMC10516786/ /pubmed/37639057 http://dx.doi.org/10.1007/s10620-023-08063-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by-nc/4.0/Open Access This article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Original Article
Chiorean, Michael
Ha, Christina
Hur, Peter
Sharma, Puza P.
Gruben, David
Khan, Nabeel H.
Experience with Tofacitinib in Patients with Ulcerative Colitis: Data from a United States Claims Database
title Experience with Tofacitinib in Patients with Ulcerative Colitis: Data from a United States Claims Database
title_full Experience with Tofacitinib in Patients with Ulcerative Colitis: Data from a United States Claims Database
title_fullStr Experience with Tofacitinib in Patients with Ulcerative Colitis: Data from a United States Claims Database
title_full_unstemmed Experience with Tofacitinib in Patients with Ulcerative Colitis: Data from a United States Claims Database
title_short Experience with Tofacitinib in Patients with Ulcerative Colitis: Data from a United States Claims Database
title_sort experience with tofacitinib in patients with ulcerative colitis: data from a united states claims database
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10516786/
https://www.ncbi.nlm.nih.gov/pubmed/37639057
http://dx.doi.org/10.1007/s10620-023-08063-4
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