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Tofacitinib in patients with moderate-to-severe chronic plaque psoriasis: long-term safety and efficacy in an open-label extension study.
Valenzuela, F; Korman, N J; Bissonnette, R; Bakos, N; Tsai, T-F; Harper, M K; Ports, W C; Tan, H; Tallman, A; Valdez, H; Gardner, A C.
Afiliación
  • Valenzuela F; Department of Dermatology, University of Chile Clinical Hospital, Santiago, Chile.
  • Korman NJ; Probity Medical Research, Santiago, Chile.
  • Bissonnette R; University Hospitals Case Medical Center, Cleveland, OH, U.S.A.
  • Bakos N; Innovaderm Research, Montreal, QC, Canada.
  • Tsai TF; Allergo-Derm Bakos Kft, Szolnok, Hungary.
  • Harper MK; Department of Dermatology, National Taiwan University Hospital, Taipei, Taiwan.
  • Ports WC; Pfizer Inc, Cambridge, MA, U.S.A.
  • Tan H; Pfizer Inc, Groton, CT, U.S.A.
  • Tallman A; Pfizer Inc, Groton, CT, U.S.A.
  • Valdez H; Pfizer Inc, New York, NY, U.S.A.
  • Gardner AC; Pfizer Inc, New York, NY, U.S.A.
Br J Dermatol ; 179(4): 853-862, 2018 10.
Article en En | MEDLINE | ID: mdl-29782642
BACKGROUND: Tofacitinib is an oral Janus kinase inhibitor. Final safety and efficacy data from an open-label extension study of tofacitinib in psoriasis are reported. OBJECTIVES: To evaluate the long-term safety and durability of efficacy of tofacitinib in adults with moderate-to-severe chronic plaque psoriasis. METHODS: Eligible patients who completed qualifying phase II/III tofacitinib studies received tofacitinib 10 mg twice daily (q12h) until month 3; subsequently, the dose could be adjusted by investigators to either 5 or 10 mg q12h. Adverse events (AEs) are reported up to month 66 and laboratory data up to month 54. Efficacy end points up to month 54 included Physician's Global Assessment of 'clear' or 'almost clear' (PGA response) and 75% improvement in Psoriasis Area and Severity Index (PASI 75). RESULTS: Overall, 2867 patients received tofacitinib, with a median treatment duration of 35·6 months. Adverse events (AEs) and serious AEs were reported in 82·5% and 13·7% of patients, respectively; 13·9% of patients discontinued owing to AEs; and 29 patients died. Incidence rates (patients with event/100 patient-years) were 1·16 for serious infections, 0·67 for malignancies and 0·26 for major adverse cardiovascular events. After initial changes in qualifying studies, most laboratory parameters were generally stable over 54 months. PGA response was achieved by 52-62% of patients and PASI 75 by 56-74% of patients at each study visit through month 54. CONCLUSIONS: In patients with psoriasis, the safety profile of tofacitinib over 66 months was similar to previous reports in phase III studies and efficacy was sustained through 54 months (NCT01163253).
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Piperidinas / Psoriasis / Pirimidinas / Pirroles / Inhibidores de Proteínas Quinasas / Efectos Colaterales y Reacciones Adversas Relacionados con Medicamentos Tipo de estudio: Clinical_trials / Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Br J Dermatol Año: 2018 Tipo del documento: Article País de afiliación: Chile Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Piperidinas / Psoriasis / Pirimidinas / Pirroles / Inhibidores de Proteínas Quinasas / Efectos Colaterales y Reacciones Adversas Relacionados con Medicamentos Tipo de estudio: Clinical_trials / Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Br J Dermatol Año: 2018 Tipo del documento: Article País de afiliación: Chile Pais de publicación: Reino Unido