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Hydroxychloroquine,
Hydroxyurea and Didanosine as Initial Therapy for HIV Patients with
Low Viral Load: A Useful Strategy for Delaying HAART?
The
aim of the current study to evaluate the long-term safety and efficacy
of the combination of hydroxychloroquine, hydroxyurea and didanosine/ddI
(Videx).
The
researchers recruited antiretroviral-naive patients with viral loads
less than 100 000 HIV-1 RNA copies/mL and CD4 counts greater
than 150 cells/microliter. All patients received hydroxychloroquine
(200 mg), hydroxyurea (500 mg) and didanosine (125 200 mg) twice
daily.
Clinical
and laboratory safety assessments and measurements of viral load
and CD4 count were made at regular intervals, and genotypic resistance testing was performed on samples with detectable
viral load at 48, 96 and 144 weeks.
Results
Fourteen
of the 17 patients who commenced therapy remained on treatment at
144 weeks.
Treatment
was well tolerated but caused neutropenia,
usually mild and transient, in 12 patients (71%). Mean viral load
was reduced by 1.6 log10 copies/mL below baseline
(P<0.001), eight patient
s
(47%) had undetectable viral load (<400 copies/mL), and
two patients (12%) had detectable viral load but no detectable resistance
mutations at week 144.
Four
patients (24%) had detectable viral load together with major resistance
mutations (three with both 74 V and 184 V, and one with
both 62 V and 65R) at week 144, but still had viral load suppression
below baseline. Mean CD4 count was increased by 106 cells/microliter
above baseline (P=0.07) at week 144.
Conclusions
In
conclusion, the authors write, “This novel and well-tolerated combination
controls viral replication during long-term follow up, with development
of few resistance mutations. With careful monitoring it may be a
useful strategy for delaying highly active antiretroviral therapy
(HAART) and associated toxicity in selected patients with low initial
viral loads.”
02/09/05
Reference
N
I Paton and J Aboulhab. Hydroxychloroquine, hydroxyurea and didanosine
as initial therapy for HIV-infected patients with low viral load:
safety, efficacy and resistance profile after 144 weeks. HIV Medicine
6(1): 13-20.
January 2005.
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