Eficacia y seguridad de abacavir más lamivudina didanosina en comparación con más estavudina en combinación con un inhibidor de la proteasa, un inhibidor no nucleósido de la transcriptasa inversa, o ambos, en las personas VIH-1 positivas sin tratamiento antirretroviral previo.

Categoría Estudio primario
RevistaHIV clinical trials
Año 2005
Cargando información sobre las referencias

PURPOSE:

The combination of abacavir + lamivudine (ABC+3TC) versus didanosine + stavudine (ddI+d4T), each combined with other classes of antiretrovirals (ARVs) in ARV-naive patients, was compared for the combined endpoint of time to plasma HIV RNA >50 copies/mL (at or after the 8-month visit) or death (primary endpoint) in a nested substudy of an ongoing multicenter randomized trial.

METHOD:

The substudy enrolled 182 patients; mean HIV RNA and CD4+ cell counts at baseline were 5.1 log10 copies/mL and 212 cells/mm3, respectively.

RESULTS:

After a median follow-up of 28 months, rates of primary endpoint were 57.2 and 67.8 per 100 person-years for the ABC+3TC and ddI+d4T groups (hazard ratio [HR]=0.81, 95% confidence interval [CI] 0.58-1.14, p=.23).

CONCLUSION:

There was a trend for treatments containing ABC+3TC to be better than treatments containing ddI+d4T with respect to HIV RNA decreases, CD4+ cell count increases, and tolerability.
Epistemonikos ID: d35eb9b8023a4547182f0bb296a4db3923784ce2
First added on: Jun 08, 2011