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Telaprevir in the Treatment of Acute Hepatitis C Virus Infection in HIV-Infected Men

Authors :
Joseph Olivieri
Donald Gardenier
Robert Cohen
Jose Lares-Guia
Richie Tran
Lembitu Sorra
Robert Chavez
Punyadech Photangtham
Daniel S. Fierer
Livette Johnson
Paul C. Bellman
Rona Vail
Randy Levine
Patrick Dalton
Rita Chow
Oscar Klein
Alicia Stivala
Donald Kaminsky
Douglas T. Dieterich
Anita Radix
William Shay
Gal Mayer
Susanne Burger
Gabriela Rodriguez-Caprio
Ward Carpenter
Erik Mortensen
Krisczar Bungay
Michel Ng
Ricky Hsu
Susan Weiss
Terry Farrow
Martin Markowitz
Nirupama Somasundaram
Melissa Wiener
William Mandell
Francis Wallach
Michael P. Mullen
Daniel Bowers
John Dellosso
Adrian Demidont
Wouter O. van Seggelen
Eddie Meraz
Eric Leach
Juan Bailey
Stuart Haber
Charles Paolino
Rosanne M. Hijdra
Amisha Malhotra
SI Rapaport
Lawrence Hitzeman
Antonio Urbina
Sneha Jacob
Alison J. Uriel
Andrea D. Branch
Jeffrey C. Kwong
Rodolfo Guadron
Larisa Litvinova
Eileen Donlon
Wen Wang
Lawrence Higgins
Victor Inada
Damaris C. Carriero
Barbara Johnston
Bisher Akil
Stephen Dillon
Shirish Huprikar
David G. Cassagnol
George Psevdos
Irina Linetskaya
Source :
Clinical Infectious Diseases. 58:873-879
Publication Year :
2013
Publisher :
Oxford University Press (OUP), 2013.

Abstract

(See the Editorial Commentary by Zeremski et al on pages 880–2.) Hepatitis C virus (HCV) chronically infects an estimated 5.2 million people in the United States and 170 million people worldwide [1]. However, as most initial (“acute”) infections are completely asymptomatic, newly infected people are rarely identified. The importance of finding these newly HCV-infected people during the acute phase was made clear in the seminal paper by Jaeckel et al [2] that showed a nearly 100% sustained virologic response (SVR) rate using just 24 weeks of interferon alone, an SVR rate many times higher than that of chronically infected patients at that time, and with just half the duration of interferon [3]. We are now faced with an entirely new group of patients who are becoming HCV infected in the international epidemic of sexually transmitted HCV infection among human immunodeficiency virus (HIV)–infected men who have sex with men (MSM). Published cure rates after treatment of acute HCV in these men, using pegylated interferon (peg-IFN) plus ribavirin (RBV) for 24–48 weeks’ duration, are not as good as those of Jaeckel et al [2], ranging from 53% to 83% [4–15], but are clearly better than the 27%–40% success rates in treatment of chronic HCV in HIV-infected men [16, 17]. Still, even with 48 weeks of treatment in many of these studies of acute HCV, fewer than two-thirds of patients achieved SVR, leaving a large proportion of these men uncured, with the possibility of experiencing rapidly advancing liver disease [18–21] and of infecting others and further propagating the epidemic. With the commercial availability of telaprevir (TVR) in the United States, we hypothesized that its potent activity against genotype 1 HCV would allow us to further shorten the treatment period while also improving the SVR rate. We therefore undertook a study of a 12-week treatment course with a combination of TVR, peg-IFN, and RBV in HIV-infected MSM with newly acquired genotype 1 HCV.

Details

ISSN :
15376591 and 10584838
Volume :
58
Database :
OpenAIRE
Journal :
Clinical Infectious Diseases
Accession number :
edsair.doi.dedup.....3354c7a784d358145bd551d713f65ba4