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Safety of baricitinib for the treatment of rheumatoid arthritis over a median of 4.6 and up to 9.3 years of treatment: final results from long-term extension study and integrated database.
Taylor, Peter C; Takeuchi, Tsutomu; Burmester, Gerd R; Durez, Patrick; Smolen, Josef S; Deberdt, Walter; Issa, Maher; Terres, Jorge Ross; Bello, Natalia; Winthrop, Kevin L.
Afiliação
  • Taylor PC; Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, UK peter.taylor@kennedy.ox.ac.uk.
  • Takeuchi T; Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine Graduate School of Medicine, Shinjuku-ku, Japan.
  • Burmester GR; Rheumatology and Clinical Immunology, Charite - Universitätsmedizin Berlin, Berlin, Germany.
  • Durez P; Division of Rheumatology, Cliniques universitaires Saint-Luc, Brussels, Belgium.
  • Smolen JS; Division of Rheumatology, Department of Medicine III, Medical University of Vienna, Vienna, Austria.
  • Deberdt W; Eli Lilly and Company, Indianapolis, Indiana, USA.
  • Issa M; Eli Lilly and Company, Indianapolis, Indiana, USA.
  • Terres JR; Eli Lilly and Company, Indianapolis, Indiana, USA.
  • Bello N; Eli Lilly and Company, Indianapolis, Indiana, USA.
  • Winthrop KL; Schools of Medicine and Public Health, Oregon Health & Sciences University, Portland, Oregon, USA.
Ann Rheum Dis ; 81(3): 335-343, 2022 03.
Article em En | MEDLINE | ID: mdl-34706874
OBJECTIVE: To report long-term safety from the completed extension trial of baricitinib, an oral selective Janus kinase inhibitor, in patients with active rheumatoid arthritis (RA). METHODS: Treatment-emergent adverse events are summarised from an integrated database (9 phase III/II/Ib and 1 long-term extension) of patients who received any baricitinib dose (All-bari-RA). Standardised incidence ratio (SIR) for malignancy (excluding non-melanoma skin cancer (NMSC)) and standardised mortality ratio (SMR) were estimated. Additional analysis was done in a subset of patients who had ever taken 2 mg or 4 mg baricitinib. RESULTS: 3770 patients received baricitinib (14 744 patient-years of exposure (PYE)). All-bari-RA incidence rates (IRs) per 100 patient-years at risk were 2.6, 3.0 and 0.5 for serious infections, herpes zoster and major adverse cardiovascular events (MACE), respectively. In patients aged ≥50 with ≥1 cardiovascular risk factor, the IR for MACE was 0.77 (95% CI 0.56 to 1.04). The IR for malignancy (excluding NMSC) during the first 48 weeks was 0.6 and remained stable thereafter (IR 1.0). The SIR for malignancies excluding NMSC was 1.07 (95% CI 0.90 to 1.26) and the SMR was 0.74 (95% CI 0.59 to 0.92). All-bari-RA IRs for deep vein thrombosis (DVT)/pulmonary embolism (PE), DVT and PE were 0.5 (95% CI 0.38 to 0.61), 0.4 (95% CI 0.26 to 0.45) and 0.3 (95% CI 0.18 to 0.35), respectively. No clear dose differences were noted for exposure-adjusted IRs (per 100 PYE) for deaths, serious infections, DVT/PE and MACE. CONCLUSIONS: In this integrated analysis including long-term data of baricitinib from 3770 patients (median 4.6 years, up to 9.3 years) with active RA, baricitinib maintained a similar safety profile to earlier analyses. No new safety signals were identified. TRIAL REGISTRATION NUMBER: NCT01185353, NCT00902486, NCT01469013, NCT01710358, NCT02265705, NCT01721044, NCT01721057, NCT01711359 and NCT01885078.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Artrite Reumatoide / Purinas / Pirazóis / Sulfonamidas / Azetidinas / Antirreumáticos / Efeitos Colaterais e Reações Adversas Relacionados a Medicamentos / Inibidores de Janus Quinases Tipo de estudo: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Ann Rheum Dis Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Artrite Reumatoide / Purinas / Pirazóis / Sulfonamidas / Azetidinas / Antirreumáticos / Efeitos Colaterais e Reações Adversas Relacionados a Medicamentos / Inibidores de Janus Quinases Tipo de estudo: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Ann Rheum Dis Ano de publicação: 2022 Tipo de documento: Article