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DOI 10.1016/j.semarthrit.2026.152946

Медицинская библиотека · Seminars in arthritis and rheumatism · 2026

Evolution of Janus Kinase inhibitors (JAKi) prescriptions since 2015 in an international collaboration of rheumatoid arthritis registers (the 'JAK-pot' study): effect of regulatory warnings.

Mongin Denis, Aymon Romain, Choquette Denis, Coupal Louis, Codreanu Catalin, Iannone Florenzo, Provan Sella, Kvien Tore K, Fritsch-Stork Ruth, Nordström Dan, Pavelka Karel, Závada Jakub, Pombo-Suarez Manuel, Otero-Varela Lucia, Sousa Elsa, Rotar Ziga, Sidiropoulos Prodromos, Bertsias Antonios, Courvoisier Delphine S, Finckh Axel, Lauper Kim, Elkayam Ori, Furer Victoria

СтатьяМногоцентровое исследованиеНаблюдательное исследованиеПеревод в очереди

Аннотация

BACKGROUND

Janus kinase inhibitors (JAKi) are effective for treating rheumatoid arthritis (RA), but post-marketing safety concerns have triggered regulatory warnings and updated guidelines. The impact of these communications on real-world prescribing remains unclear.

OBJECTIVES

To assess the impact of major regulatory safety warnings on the initiation, discontinuation, and switching patterns of JAKi in RA patients, using data from 12 national registries.

METHODS

This observational study analyzed 55,365 treatment courses (12559 JAKi and 42806 other bDMARDs) from 40,019 adult RA patients between 2015 and 2024. Segmented regression models examined trends around eight major regulatory events. Logistic generalized estimating equations (GEE), adjusted for demographic, disease, and treatment variables, were used. Sensitivity and subgroup analyses, including at-risk populations (age ≥65 with cardiovascular risk factors), were conducted.

RESULTS

JAKi use rose from <1 % in 2015 to >20 % by 2024, with slowdowns after the 2019 FDA and 2022 EMA warnings. Initiation trends significantly slowed after the first FDA warning and the publication of increased risks for MACE and cancer in early 2021, primarily affecting tofacitinib. Discontinuations surged following the EMA's 2022 warning, again mainly affecting tofacitinib. Upadacitinib initiations also declined, and discontinuations increased after the publication of the ORAL Surveillance trial. Baricitinib use appeared to be less impacted by the safety signals, while filgotinib use steadily increased. Among the at-risk population, the rate of JAKi discontinuation significantly rose after the 2019 EMA warning.

CONCLUSIONS

Regulatory safety communications significantly influenced real-world JAKi prescribing patterns. Tofacitinib was most affected through both declines in initiation and increases in discontinuation.

Для цитирования: Mongin Denis, Aymon Romain, Choquette Denis, Coupal Louis, Codreanu Catalin, Iannone Florenzo, Provan Sella, Kvien Tore K, Fritsch-Stork Ruth, Nordström Dan, Pavelka Karel, Závada Jakub, Pombo-Suarez Manuel, Otero-Varela Lucia, Sousa Elsa, Rotar Ziga, Sidiropoulos Prodromos, Bertsias Antonios, Courvoisier Delphine S, Finckh Axel, Lauper Kim, Elkayam Ori, Furer Victoria. Evolution of Janus Kinase inhibitors (JAKi) prescriptions since 2015 in an international collaboration of rheumatoid arthritis registers (the 'JAK-pot' study): effect of regulatory warnings.. Seminars in arthritis and rheumatism. 2026. DOI: 10.1016/j.semarthrit.2026.152946.

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