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Disease Progression in Patients With Hepatitis C Virus Infection Treated With Direct-Acting Antiviral Agents.
Mendizabal, Manuel; Piñero, Federico; Ridruejo, Ezequiel; Herz Wolff, Fernando; Anders, Margarita; Reggiardo, Virginia; Ameigeiras, Beatriz; Palazzo, Ana; Alonso, Cristina; Schinoni, María Isabel; Videla Zuain, María Grazia; Tanno, Federico; Figueroa, Sebastián; Santos, Luisa; Peralta, Mirta; Soza, Alejandro; Vistarini, Cecilia; Adrover, Raúl; Fernández, Nora; Perez, Daniela; Hernández, Nelia; Estepo, Claudio; Bruno, Andres; Descalzi, Valeria; Sixto, Marcela; Borzi, Silvia; Cocozzella, Daniel; Zerega, Alina; de Araujo, Alexandre; Varón, Adriana; Rubinstein, Fernando; Cheinquer, Hugo; Silva, Marcelo.
Afiliación
  • Mendizabal M; Hepatology and Liver Transplant Unit, Hospital Universitario Austral, Pilar, Argentina. Electronic address: mmendiza@cas.austral.edu.ar.
  • Piñero F; Hepatology and Liver Transplant Unit, Hospital Universitario Austral, Pilar, Argentina.
  • Ridruejo E; Hepatology and Liver Transplant Unit, Hospital Universitario Austral, Pilar, Argentina; Centro de Educación Médica e Investigaciones Clínicas, CEMIC, Ciudad de Buenos Aires, Argentina.
  • Herz Wolff F; Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
  • Anders M; Hospital Alemán, Ciudad de Buenos Aires, Argentina.
  • Reggiardo V; Hospital Provincial del Centenario, Rosario, Argentina.
  • Ameigeiras B; Hospital Ramos Mejía, Ciudad de Buenos Aires, Argentina.
  • Palazzo A; Hospital Padilla, Tucumán, Argentina.
  • Alonso C; Hepatology and Liver Transplant Unit, Hospital Universitario Austral, Pilar, Argentina.
  • Schinoni MI; Universidade Federal do Bahia, Salvador do Bahia, Brazil.
  • Videla Zuain MG; Hospital Zubizarreta, Ciudad de Buenos Aires, Argentina.
  • Tanno F; Hospital Provincial del Centenario, Rosario, Argentina.
  • Figueroa S; Hospital Arturo Oñativia, Salta, Argentina.
  • Santos L; Fundación Cardioinfantil, Bogotá, Colombia.
  • Peralta M; Hospital Francisco J. Muñiz, Ciudad de Buenos Aires, Argentina.
  • Soza A; Hospital Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Vistarini C; Hospital Ramos Mejía, Ciudad de Buenos Aires, Argentina.
  • Adrover R; Hospital San Roque, La Plata, Argentina.
  • Fernández N; Hospital Británico, Ciudad de Buenos Aires, Argentina.
  • Perez D; Hospital Padilla, Tucumán, Argentina.
  • Hernández N; Hospital de Clínicas, Montevideo, Uruguay.
  • Estepo C; Hospital Cosme Argerich, Ciudad de Buenos Aires, Argentina.
  • Bruno A; Hospital Cosme Argerich, Ciudad de Buenos Aires, Argentina.
  • Descalzi V; Fundación Favaloro, Ciudad de Buenos Aires, Argentina.
  • Sixto M; Hospital Jose María Cullen, Santa Fe, Argentina.
  • Borzi S; Hospital Rossi, La Plata, Argentina.
  • Cocozzella D; Hospital San Roque, La Plata, Argentina.
  • Zerega A; Sanatorio Allende, Córdoba, Argentina.
  • de Araujo A; Hospital de Clínicas de Porto Alegre, Brazil.
  • Varón A; Hospital Francisco J. Muñiz, Ciudad de Buenos Aires, Argentina.
  • Rubinstein F; Instituto de Efectividad Clínica Sanitaria, Buenos Aires, Argentina.
  • Cheinquer H; Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
  • Silva M; Hepatology and Liver Transplant Unit, Hospital Universitario Austral, Pilar, Argentina.
Clin Gastroenterol Hepatol ; 18(11): 2554-2563.e3, 2020 10.
Article en En | MEDLINE | ID: mdl-32113892
ABSTRACT
BACKGROUND &

AIMS:

Little is known about how a sustained virologic response (SVR) to treatment of hepatitis C virus infection with direct-acting antivirals (DAAs) affects patient mortality and development of new liver-related events. We aimed to evaluate the incidence of disease progression in patients treated with DAAs.

METHODS:

We performed a prospective multicenter cohort study of 1760 patients who received DAA treatment at 23 hospitals in Latin America, from May 1, 2016, through November 21, 2019. We excluded patients with a history of liver decompensation, hepatocellular carcinoma (HCC), or solid-organ transplantation. Disease progression after initiation of DAA therapy included any of the following new events liver decompensation, HCC, liver transplantation, or death. Evaluation of variables associated with the primary outcome was conducted using a time-dependent Cox proportional hazards models.

RESULTS:

During a median follow-up period of 26.2 months (interquartile range, 15.3-37.5 mo), the overall cumulative incidence of disease progression was 4.1% (95% CI, 3.2%-5.1%), and after SVR assessment was 3.6% (95% CI, 2.7%-4.7%). Baseline variables associated with disease progression were advanced liver fibrosis (hazard ratio [HR], 3.4; 95% CI, 1.2-9.6), clinically significant portal hypertension (HR, 2.1; 95% CI, 1.2-3.8), and level of albumin less than 3.5 mg/dL (HR, 4.1; 95% CI, 2.3-7.6), adjusted for SVR achievement as a time covariable. Attaining an SVR reduced the risk of liver decompensation (HR, 0.3; 95% CI, 0.1-0.8; P = .016) and de novo HCC (HR, 0.2; 95% CI, 0.1%-0.8%; P = .02) in the overall cohort.

CONCLUSIONS:

Treatment of hepatitis C virus infection with DAAs significantly reduces the risk of new liver-related complications and should be offered to all patients, regardless of disease stage. Clinicaltrials.gov NCT03775798.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Carcinoma Hepatocelular / Hepatitis C Crónica / Neoplasias Hepáticas Tipo de estudio: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Clin Gastroenterol Hepatol Asunto de la revista: GASTROENTEROLOGIA Año: 2020 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Carcinoma Hepatocelular / Hepatitis C Crónica / Neoplasias Hepáticas Tipo de estudio: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Clin Gastroenterol Hepatol Asunto de la revista: GASTROENTEROLOGIA Año: 2020 Tipo del documento: Article