作者
María Chaparro,Iria Baston-Rey,Estela Fernández-Salgado,Javier González García,Laura Ramos,María Teresa Diz-Lois Palomares,Federico Argüelles-Arias,Eva Iglesias Flores,Mercedes Cabello,Saioa Rubio Iturria,Andrea Núñez Ortiz,Mara Charro,Daniel Ginard,Carmen Dueñas Sadornil,Olga Merino Ochoa,David Busquets,Eduardo Iyo,Ana Gutiérrez Casbas,Patricia Ramírez de la Piscina,Marta Maia Boscá-Watts,Maite Arroyo,María José García,Esther Hinojosa,Jordi Gordillo,Pilar Martínez Montiel,Benito Velayos Jiménez,Cristina Quílez Ivorra,Juan María Vázquez Morón,José María Huguet,Yago González-Lama,Ana Isabel Muñagorri Santos,Víctor Manuel Amo,María Dolores Martín-Arranz,Fernando Bermejo,Jesús Martínez Cadilla,Cristina Rubín de Célix,Paola Fradejas Salazar,Antonio López San Román,Nuria Jiménez,Santiago García López,Anna Figuerola,Itxaso Jiménez,Francisco José Martínez Cerezo,Carlos Taxonera,Pilar Varela,R de Francisco,David Monfort,Gema Molina Arriero,Alejandro Hernández Camba,Javier P. Gisbert,Manuel Van Domselaar,Ramón Pajares Villarroya,Alejandro Núñez,Francisco Rodríguez Moranta,Ignacio Marín-Jiménez,Virginia Robles Alonso,María Del Mar Martín Rodríguez,Patricia Camo-Monterde,Iván García Tercero,Mercedes Navarro Llavat,Lara Arias García,Daniel Hervías Cruz,Sara Sulleiro,Cynthia Novella,Eugenia Vispo,Manuel Barreiro-de Acosta,Javier P. Gisbert
摘要
Large real-world-evidence studies are required to confirm the durability of response, effectiveness, and safety of ustekinumab in Crohn's disease (CD) patients in real-world clinical practice.A retrospective, multicentre study was conducted in Spain in patients with active CD who had received ≥1 intravenous dose of ustekinumab for ≥6 months. Primary outcome was ustekinumab retention rate; secondary outcomes were to identify predictive factors for drug retention, short-term remission (week 16), loss of response and predictive factors for short-term efficacy and loss of response, and ustekinumab safety.A total of 463 patients were included. Mean baseline Harvey-Bradshaw Index was 8.4. A total of 447 (96.5%) patients had received prior biologic therapy, 141 (30.5%) of whom had received ≥3 agents. In addition, 35.2% received concomitant immunosuppressants, and 47.1% had ≥1 abdominal surgery. At week 16, 56% had remission, 70% had response, and 26.1% required dose escalation or intensification; of these, 24.8% did not subsequently reduce dose. After a median follow-up of 15 months, 356 (77%) patients continued treatment. The incidence rate of ustekinumab discontinuation was 18% per patient-year of follow-up. Previous intestinal surgery and concomitant steroid treatment were associated with higher risk of ustekinumab discontinuation, while a maintenance schedule every 12 weeks had a lower risk; neither concomitant immunosuppressants nor the number of previous biologics were associated with ustekinumab discontinuation risk. Fifty adverse events were reported in 39 (8.4%) patients; 4 of them were severe (2 infections, 1 malignancy, and 1 fever).Ustekinumab is effective and safe as short- and long-term treatment in a refractory cohort of CD patients in real-world clinical practice.This large retrospective study demonstrated the short- and long-term effectiveness and safety of ustekinumab in patients with Crohn’s disease in real-world clinical practice, including those with refractory disease.