Publicaciones científicas

Effectiveness and safety of ombitasvir, paritaprevir, ritonavir ± dasabuvir ± ribavirin: An early access programme for Spanish patients with genotype 1/4 chronic hepatitis C virus infection

Perelló C (1,2), Carrión JA (3,4, Ruiz-Antorán B (1), Crespo J (5,6), Turnes J (7), Llaneras J (8), Lens S (2,9), Delgado M (10), García-Samaniego J (2,11), García-Paredes F (12), Fernández I (13), Morillas RM (2,14), Rincón D (2,15), Porres JC (16), Prieto M (2,17), Lázaro Ríos M (18), Fernández-Rodríguez C (19), Hermo JA (20), Rodríguez M (21), Herrero JI (2,22), Ruiz P (23), Fernández JR (24), Macías M (25), Pascasio JM (2,26), Moreno JM (27), Serra MÁ (28,29), Arenas J (30), Real Y (31), Jorquera F (2,32), Calleja JL 1,2,33; Spanish Collaborative Group for the Study of the Use of Hepatitis C Direct-Acting Drugs.
(1) Hospital Universitario Puerta de Hierro Majadahonda, IDIPHIM, Madrid, Spain.
(2) CIBERehd, Madrid, Spain.
(3) Hospital del Mar, IMIM (Hospital del Mar Medical Research Institute), Barcelona, Spain.
(4) Universitat Autonoma de Barcelona, Barcelona, Spain.
(5) Hospital Universitario Marqués de Valdecilla, IDIVAL, Santander, Spain.
(6) Facultad de Medicina, Universidad de Cantabria, Santander, Spain.
(7) Complejo Hospitalario Universitario de Pontevedra and IISGS, Pontevedra, Spain.
(8) Hospital Universitario Vall D'Hebrón, Barcelona, Spain.
(9) Hospital Clinic, IDIBAPS, Barcelona, Spain.
(10) Hospital Universitario A Coruña, A Coruña, Spain.
(11) Hospital Universitario La Paz, Madrid, Spain.
(12) Hospital Universitario Río Hortega, Valladolid, Spain.
(13) Hospital Universitario Doce de Octubre, Madrid, Spain.
(14) Hospital Universitario Germans Trias i Pujol, Badalona, Spain.
(15) Hospital General Universitario Gregorio Marañón, Madrid, Spain.
(16) Hospital Universitario Fundación Jiménez Díaz, Madrid, Spain.
(17) Hospital Universitari i Politècnic La Fe, Valencia, Spain.
(18) Hospital Universitario Miguel Servet, Zaragoza, Spain.
(19) Hospital Universitario Alcorcón, Universidad Rey Juan Carlos, Madrid, Spain.
(20) Hospital Álvaro Cunqueiro, Vigo, Spain.
(21) Hospital Universitario Central de Asturias, Oviedo, Spain.
(22) Clínica Universidad de Navarra, Instituto de Investigación Sanitaria de Navarra (IdiSNA), Pamplona, Spain.
(23) Hospital Universitario Basurto, Bilbao, Spain.
(24) Hospital Universitario de Cruces, Bilbao, Spain.
(25) Hospital Universitario Puerta del Mar, Cádiz, Spain.
(26) Hospital Universitario Virgen del Rocío, Sevilla, Spain.
(27) Complejo Hospitalario Albacete, Albacete, Spain.
(28) Hospital Universitario Clínico Valencia, INCLIVA, Valencia, Spain.
(29) University of Valencia, Valencia, Spain.
(30) Hospital Universitario Donostia, Donostia, Spain.
(31) Hospital Universitario La Princesa, Madrid, Spain.
(32) Complejo Asistencial de León, IBIOMED, León, Spain.
(33) Universidad Autónoma de Madrid, Madrid, Spain. 

Revista: Journal of Viral Hepatitis

Fecha: 15/12/2016

Hepatología

RESUMEN

Over the last 5 years, therapies for hepatitis C virus (HCV) infection have improved significantly, achieving sustained virologic response (SVR) rates of up to 100% in clinical trials in patients with HCV genotype 1.

We investigated the effectiveness and safety of ombitasvir/paritaprevir/ritonavir±dasabuvir in an early access programme.

This was a retrospective, multicentre, national study that included 291 treatment-naïve and treatment-experienced patients with genotype 1 or 4 HCV infection. Most patients (65.3%) were male, and the mean age was 57.5 years.

The mean baseline viral load was 6.1 log, 69.8% had HCV 1b genotype, 72.9% had cirrhosis and 34.7% were treatment-naïve. SVR at 12 weeks posttreatment was 96.2%. Four patients had virological failure (1.4%), one leading to discontinuation. There were no statistical differences in virological response according to genotype or liver fibrosis.

Thirty patients experienced serious adverse events (SAEs) (10.3%), leading to discontinuation in six cases. Hepatic decompensation was observed in five patients. Four patients died during treatment or follow-up, three of them directly related to liver failure.

Multivariate analyses showed a decreased probability of achieving SVR associated with baseline albumin, bilirubin and Child-Pugh score B, and a greater probability of developing SAEs related to age and albumin.

This combined therapy was highly effective in clinical practice with an acceptable safety profile and low rates of treatment discontinuation.

CITA DEL ARTÍCULO  J Viral Hepat. 2016 Dec 15. doi: 10.1111/jvh.12637

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