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Safety of biologic therapy in combination with methotrexate in moderate to severe psoriasis: a cohort study from the BIOBADADERM registry.
Lluch-Galcerá, Juan José; Carrascosa, Jose Manuel; González-Quesada, Alicia; Rivera-Díaz, Raquel; Sahuquillo-Torralba, Antonio; Llamas-Velasco, Mar; Gómez-García, Francisco José; Herrera-Acosta, Enrique; de la Cueva, Pablo; Baniandrés-Rodríguez, Ofelia; Lopez-Estebaranz, Jose Luis; Belinchón, Isabel; Ferrán, Marta; Mateu, Almudena; Rodríguez, Lourdes; Riera-Monroig, Josep; Abalde-Pintos, M Teresa; Carretero, Gregorio; García-Donoso, Carmen; Pujol-Marco, Conrad; Del Alcázar, Elena; Santamaría-Domínguez, Cristina; Suárez-Pérez, Jorge Alonso; Nieto-Benito, Lula María; Ruiz-Genao, Diana Patricia; Salgado-Boquete, Laura; Descalzo, Miguel Ángel; García-Doval, Ignacio.
Afiliação
  • Lluch-Galcerá JJ; Department of Dermatology, Hospital Universitari Germans Trias i Pujol, Universitat Autònoma de Barcelona, IGTP. Badalona, Barcelona, Spain.
  • Carrascosa JM; Departament de Medicina, Universitat Autonoma de Barcelona (UAB), Barcelona, Spain.
  • González-Quesada A; Department of Dermatology, Hospital Universitari Germans Trias i Pujol, Universitat Autònoma de Barcelona, IGTP. Badalona, Barcelona, Spain.
  • Rivera-Díaz R; Departament de Medicina, Universitat Autonoma de Barcelona (UAB), Barcelona, Spain.
  • Sahuquillo-Torralba A; Department of Dermatology, Hospital Universitario de Gran Canaria Dr. Negrín, Las Palmas de Gran Canaria, Islas Canarias, Spain.
  • Llamas-Velasco M; Department of Dermatology, Hospital Universitario 12 de Octubre, Universidad Complutense, Madrid, Spain.
  • Gómez-García FJ; Department of Dermatology, Hospital Universitario y Politécnico La Fe, Valencia,Spain.
  • Herrera-Acosta E; Department of Dermatology, Hospital Universitario de La Princesa, Instituto de Investigación Sanitaria de La Princesa (IIS-LP), Madrid,Spain.
  • de la Cueva P; Department of Dermatology, Hospital Universitario Reina Sofía, Córdoba, Spain.
  • Baniandrés-Rodríguez O; Department of Dermatology, Hospital Universitario Virgen de la Victoria, Málaga, Spain.
  • Lopez-Estebaranz JL; Department of Dermatology, Hospital Universitario Infanta Leonor, Madrid, Spain.
  • Belinchón I; Department of Dermatology, CEIMI, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
  • Ferrán M; Department of Dermatology, Hospital Universitario Fundación Alcorcón, Alcorcón, Madrid, Spain.
  • Mateu A; Department of Dermatology, Hospital General Universitario de Alicante-ISABIAL-UMH, Alicante, Spain.
  • Rodríguez L; Department of Dermatology, Hospital del Mar, Parc de Salut Mar, Barcelona, Spain.
  • Riera-Monroig J; Department of Dermatology, Hospital Universitario Doctor Peset, Valencia, Spain.
  • Abalde-Pintos MT; Department of Dermatology, Hospital Virgen del Rocío, Seville, Spain.
  • Carretero G; Department of Dermatology, Hospital Clinic de Barcelona, UB, Barcelona, Spain.
  • García-Donoso C; Department of Dermatology, Complejo Hospitalario Universitario de Pontevedra, Pontevedra, Spain.
  • Pujol-Marco C; Department of Dermatology, Hospital Universitario de Gran Canaria Dr. Negrín, Las Palmas de Gran Canaria, Islas Canarias, Spain.
  • Del Alcázar E; Department of Dermatology, Hospital Universitario 12 de Octubre, Universidad Complutense, Madrid, Spain.
  • Santamaría-Domínguez C; Department of Dermatology, Hospital Universitario y Politécnico La Fe, Valencia,Spain.
  • Suárez-Pérez JA; Department of Dermatology, Hospital Universitari Germans Trias i Pujol, Universitat Autònoma de Barcelona, IGTP. Badalona, Barcelona, Spain.
  • Nieto-Benito LM; Departament de Medicina, Universitat Autonoma de Barcelona (UAB), Barcelona, Spain.
  • Ruiz-Genao DP; Department of Dermatology, Hospital Universitario de La Princesa, Instituto de Investigación Sanitaria de La Princesa (IIS-LP), Madrid,Spain.
  • Salgado-Boquete L; Department of Dermatology, Hospital Universitario Virgen de la Victoria, Málaga, Spain.
  • Descalzo MÁ; Department of Dermatology, CEIMI, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
  • García-Doval I; Department of Dermatology, Hospital Universitario Fundación Alcorcón, Alcorcón, Madrid, Spain.
Br J Dermatol ; 190(3): 355-363, 2024 Feb 16.
Article em En | MEDLINE | ID: mdl-37846976
BACKGROUND: Safety is an important consideration in decisions on treatment for patients with moderate-to-severe psoriasis and the study of drug safety is the main purpose of the BIOBADADERM registry. The combination of a biologic agent and a conventional systemic drug [generally methotrexate (MTX)] is a common treatment in clinical practice. However, there is a paucity of evidence from real-world practice on the safety of such combination regimens in the treatment of psoriasis. OBJECTIVES: The primary objective of this study was to ascertain whether the use of regimens combining biologic drugs with MTX in the management of moderate-to-severe psoriasis increases the risk of adverse events (AEs) or serious AEs (SAEs). We compared monotherapy using tumour necrosis factor (TNF), interleukin (IL)-17 and IL-23 inhibitors with the use of the same drugs in combination with MTX. METHODS: Using data from the BIOBADADERM registry, we compared biologic monotherapies with therapies that were combined with MTX. We estimated adjusted incidence rate ratios (aIRR) using a random effects Poisson regression with 95% confidence intervals for all AEs, SAEs, infections and serious infections and other AEs by system organ class. RESULTS: We analysed data from 2829 patients and 5441 treatment cycles, a total of 12 853 patient-years. The combination of a biologic with MTX was not associated with statistically significant increases in overall risk of AEs or SAEs in any treatment group. No increase in the total number of infections or serious infections in patients receiving combined therapy was observed for any group. However, treatment with a TNF inhibitor combined with MTX was associated with an increase in the incidence of gastrointestinal AEs (aIRR 2.50, 95% CI 1.57-3.98; P < 0.002). CONCLUSIONS: The risk of AEs and SAEs was not significantly increased in patients with moderate-to-severe psoriasis receiving different classes of biologic drugs combined with MTX compared with those on biologic monotherapy.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Psoríase / Produtos Biológicos Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Psoríase / Produtos Biológicos Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article