Baseline serum hepatitis C virus (HCV) RNA level and response at week 4 are the best predictors of relapse after treatment with pegylated interferon plus ribavirin in HIV/HCV-coinfected patients

BACKGROUND: Relapse after achieving virologic response to anti-hepatitis C virus (HCV) treatment considerably reduces sustained virologic response rates. It is unclear what the main predictors of relapse in HCV/HIV-coinfected patients are.

PATIENTS AND METHODS: The Pegasys Ribavirina España Coinfección (PRESCO) study evaluated short and extended duration of treatment for chronic hepatitis C using pegylated interferon (peg-IFN)-alpha2a at a dose of 180 microg/wk plus weight-based ribavirin (RBV) at a dose of 1000 to 1200 mg/d in HIV-infected subjects. Patients with HCV-2/3 were treated for 6 or 12 months, and patients with HCV-1/4 were treated for 12 or 18 months.

RESULTS: Of 389 patients included in the trial, end-of-treatment response was achieved by 262 (67.3%): 106 with HCV-1 (55%), 137 with HCV-2/3 (90%), and 19 with HCV-4 (41%). Six patients were lost to follow-up after completing therapy. Of the remaining 256 patients, 62 (24%) relapsed: 33% of HCV-1 patients, 18% of HCV-2/3 patients, and 21% of HCV-4 patients. In multivariate logistic regression analysis, baseline serum HCV RNA level > or =500,000 IU/mL (relative risk [RR] = 4.81, 95% confidence interval [CI]: 1.52 to 15.22; P = 0.008) and lack of rapid virologic response, defined as undetectable HCV RNA level at week 4 (RR = 2.94, 95% CI: 1.22 to 7.09; P = 0.02) were the best independent predictors of HCV relapse. Use of concomitant antiretroviral therapy also predicted relapse (P = 0.04), and a trend toward a higher relapse rate was recognized for HCV genotypes 1 and 4 versus genotypes 2 and 3 (P = 0.08). Extended treatment did not result in a lower incidence of relapse, at least for HCV genotypes 2 and 3.

CONCLUSION: High baseline serum HCV RNA level and lack of undetectable viremia at week 4 are the most significant predictors of relapse in HCV/HIV-coinfected patients treated with peg-IFN plus weight-based RBV.

Errataetall:

ErratumIn: J Acquir Immune Defic Syndr. 2008 Apr 1;47(4):528 Mariño, Angel [corrected to Mariño, Ana]

Medienart:

Artikel

Erscheinungsjahr:

2007

Erschienen:

2007

Enthalten in:

Zur Gesamtaufnahme - volume:45

Enthalten in:

Journal of acquired immune deficiency syndromes (1999) - 45(2007), 4 vom: 01. Aug., Seite 439-44

Sprache:

Englisch

Beteiligte Personen:

Núñez, Marina [VerfasserIn]
Mariño, Ana [VerfasserIn]
Mariño, Angel [VerfasserIn]
Miralles, Celia [VerfasserIn]
Berdún, Miguel A [VerfasserIn]
Sola, Julio [VerfasserIn]
Hernandez-Burruezo, Juan Jose [VerfasserIn]
Galindo, Maria Jose [VerfasserIn]
Barreiro, Pablo [VerfasserIn]
Martin-Carbonero, Luz [VerfasserIn]
Soriano, Vincent [VerfasserIn]

Themen:

3WJQ0SDW1A
49717AWG6K
Antiviral Agents
Clinical Trial
Interferon alpha-2
Interferon-alpha
Journal Article
Multicenter Study
Peginterferon alfa-2a
Polyethylene Glycols
Q46947FE7K
RNA, Viral
Recombinant Proteins
Research Support, Non-U.S. Gov't
Ribavirin

Anmerkungen:

Date Completed 27.08.2007

Date Revised 30.09.2020

published: Print

ErratumIn: J Acquir Immune Defic Syndr. 2008 Apr 1;47(4):528 Mariño, Angel [corrected to Mariño, Ana]

Citation Status MEDLINE

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM169984435