Re-treatment
of HIV/HCV Coinfected Patients with Pegylated Interferon plus
Ribavirin
By
Liz Highleyman
Approximately
half of people with chronic hepatitis C virus (HCV) infection
-- and a somewhat higher proportion of HIV/HCV coinfected people
-- do not attain SVR (continued undetectable HCV viral load
24 weeks after completing treatment) with a first course of
standard-of-care therapy consisting of pegylated
interferon plus ribavirin. The success rate is even lower
for people initially treated with a suboptimal regimen, for
example conventional rather than pegylated interferon, or interferon
monotherapy without ribavirin.
Pablo
Labarga from Hospital Carlos III in Madrid and colleagues evaluated
the safety and efficacy of standard-of-care treatment for coinfected
patients who did not achieve sustained response or relapsed
after prior suboptimal therapy.
The study included 52 chronic hepatitis C patients. Most (78%)
had hard-to-treat HCV
genotypes 1 or 4 and about half (56%) had advanced but compensated
liver fibrosis. Prior suboptimal regimens included interferon
monotherapy (20%), conventional interferon plus ribavirin (29%),
and pegylated interferon plus fixed-dose 800 mg/day ribavirin
(51%). Overall, 61% were prior non-responders and 39% were prior
relapsers.
All participants were treated with 180 mcg/week pegylated
interferon alpha-2a (Pegasys) plus weight-adjusted doses of
ribavirin (1000 mg/day if < 75 kg [about 165 lb] or 1200
mg/day if 75 kg) for 48 weeks.
Results
 |
The
overall sustained virological response rate was 30.8%. |
 |
As
expected, SVR was significantly less likely in people with
HCV genotypes 1 or 4 (19.5%) compared with genotypes 2 or
3 (72.7%). |
 |
In
a multivariate analysis, the only independent predictors
of SVR were: |
| |
 |
Genotype
2 or 3 (odds ratio 22.2; P = 0.003); |
 |
Higher
ribavirin trough concentration, or lowest level between
doses (odds ratio 3.9; P = 0.01). |
|
Based on these findings, the researchers concluded that re-treatment
with pegylated interferon alpha-2a plus weight-based ribavirin
for 12 months results in HCV clearance in nearly one-third of
HIV/HCV coinfected patients who failed a prior suboptimal course
of hepatitis C therapy.
"Patients with HCV genotypes 2/3 and those with ribavirin
plasma trough levels above 2.07 mcg/mL show the highest chances
of SVR," they added.
Department of Infectious Diseases and Pharmacology Unit,
Hospital Carlos III, Madrid, Spain; HIV Unit, Hospital San Pedro,
Logroño, Spain.
2/2/10
Reference
P
Labarga, E Vispo, P Barreiro, and others. Rate and Predictors
of Success in the Retreatment of Chronic Hepatitis C Virus in
HIV/HCV-Coinfected Patients With Prior Nonresponse or Relapse.
Journal of Acquired Immune Deficiency Syndromes (Abstract).
January 23, 2010 (Epub ahead of print).