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Clinical response to linaclotide at week 4 predicts sustained response in irritable bowel syndrome with constipation and improvements in digestive and extra-digestive symptoms.
Serrano-Falcón, Blanca; Delgado-Aros, Sílvia; Mearin, Fermín; Ciriza de Los Ríos, Constanza; Serra, Jordi; Mínguez, Miguel; Montoro Huguet, Miguel; Perelló, Antonia; Santander, Cecilio; Pérez Aisa, Ángeles; Bañón-Rodríguez, Inmaculada; Rey, Enrique.
Afiliación
  • Serrano-Falcón B; Hospital Clínico San Carlos, Instituto de Investigación Sanitaria San Carlos (IdISSC), Madrid, Spain.
  • Delgado-Aros S; Hospital del Mar, Barcelona, Spain.
  • Mearin F; Centro Médico Teknon, Barcelona, Spain.
  • Ciriza de Los Ríos C; Hospital 12 de Octubre, Madrid, Spain.
  • Serra J; University Hospital German Trias i Pujol, Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEREHD), Badalona, Spain.
  • Mínguez M; Hospital Clínico de València, Universitat de València, València, Spain.
  • Montoro Huguet M; Hospital San Jorge, Huesca, Spain.
  • Perelló A; Hospital de Viladecans, Barcelona, Spain.
  • Santander C; Hospital Universitario de La Princesa, Instituto de Investigación Sanitaria Princesa (IIS-IP), Universidad Autónoma de Madrid, Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEREHD), Madrid, Spain.
  • Pérez Aisa Á; Agencia Sanitaria Costa del Sol, Marbella, Spain.
  • Bañón-Rodríguez I; Allergan plc, Madrid, Spain.
  • Rey E; Servicio de Aparato Digestivo, Hospital Clínico San Carlos, Universidad Complutense, Instituto de Investigación Sanitaria San Carlos (IdISSC), 28040 Madrid, Spain.
Therap Adv Gastroenterol ; 12: 1756284819857358, 2019.
Article en En | MEDLINE | ID: mdl-31428193
BACKGROUND: Linaclotide is approved for the treatment of moderate-to-severe irritable bowel syndrome (IBS) with constipation (IBS-C) in adults. This study aimed to assess factors predictive of a clinical response and improvements in non-IBS symptoms with linaclotide treatment in a Spanish patient population. METHODS: In this open-label phase IIIb study, patients with moderate-to-severe IBS-C received linaclotide 290 µg once daily for 12 weeks. The primary endpoint was clinical response at week 12, defined as >30% reduction in IBS symptom severity score (IBS-SSS) or IBS-SSS <75 plus self-reported response of feeling 'better' or 'much better' versus the baseline. Digestive nonintestinal and extra-digestive symptom scores were assessed. Baseline characteristics and week 4 clinical response were assessed as predictors of week 12 clinical response. RESULTS: A total of 96 patients were eligible; 91 were female and the mean age was 47.4 years. Mean (SD) baseline IBS-SSS was 371 (72.5). In the intention-to-treat and per-protocol populations, 22.9% and 31.7% were clinical responders at week 4, respectively, and 25.0% and 36.7% were clinical responders at week 12. Digestive nonintestinal and extra-digestive symptom scores were significantly improved at weeks 4 and 12. Baseline characteristic was not associated with week 12 clinical response; however, clinical response at week 4 was predictive of response at week 12 (OR: 6.5; 95%IC: 2.1-19.8). The most common adverse event was diarrhea inclusive of loose or watery stools (35.4%). CONCLUSIONS: Linaclotide improves IBS-C symptoms, including digestive nonintestinal and extra-digestive symptoms. A clinical response at week 4 may predict response at week 12.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Diagnostic_studies / Guideline / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Therap Adv Gastroenterol Año: 2019 Tipo del documento: Article País de afiliación: España Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Diagnostic_studies / Guideline / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Therap Adv Gastroenterol Año: 2019 Tipo del documento: Article País de afiliación: España Pais de publicación: Reino Unido