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The Association of Cytopenias and Weight Loss with Hepatitis C Virus Virologic Response in HIV/HCV-Coinfected Patients Treated with PEG-IFN and RBV

Authors :
Jihad Slim MD
Donna Mildvan MD
Jian Han PhD
Eli Korner PharmD, MPH
Source :
Journal of the International Association of Providers of AIDS Care, Vol 12 (2013)
Publication Year :
2013
Publisher :
SAGE Publishing, 2013.

Abstract

Background: Pegylated interferon (PEG-IFN)/ribavirin (RBV)-related cytopenias have been associated with improved virological outcomes among hepatitis C virus (HCV)-monoinfected patients. This analysis evaluated PEG-IFN/RBV-related cytopenias with virological responses among HIV/HCV-coinfected patients. Methods: Pooled data from PARADIGM and AIDS Pegasys Ribavirin International CO-infection Trial (APRICOT) trials of HIV/HCV-infected patients treated with PEG-IFN/RBV. Virologic response was categorized as HCV RNA detectable (end of treatment nonresponders [ET-NR]) or nondetectable (end of treatment responders [ETR]). Declines in hemoglobin (Hgb), platelets, neutrophils, lymphocytes, and weight between the groups were compared via analysis of covariance and Cochran-Mantel-Haenszel test. Results: A total of 474 patients, 291 ET-NR and 183 ETR (67 relapsers, 116 with sustained virologic response), 81% male, 52% Caucasian, 88% noncirrhotic, and 67% nondetectable HIV. The ETR experienced greater Hgb declines (≥3.0 g/dL) from baseline (73.8% versus 55.0%; P < .0001), neutrophils ≤1 and ≤ 0.5 × 10 9 /L (66.1% versus 56.4%; P = .0334 and 42.6% versus 33.3%; P = .0312, respectively), and lymphocytes ≤1.5 and ≤0.5 × 10 9 /L (99.5% versus 87.6%; P < .0001 and 24.6% versus 14.9%; P =.0079, respectively). Conclusions: The HIV/HCV-coinfected patients with ETR experienced greater declines in Hgb, neutrophils, and lymphocytes than the ET-NR patients.

Details

Language :
English
ISSN :
23259574 and 23259582
Volume :
12
Database :
Directory of Open Access Journals
Journal :
Journal of the International Association of Providers of AIDS Care
Publication Type :
Academic Journal
Accession number :
edsdoj.9a5d01ca4f664263888dcdcb893402b0
Document Type :
article
Full Text :
https://doi.org/10.1177/2325957413494828