N. Gianotti et al., SMART - study on mutations and antiretroviral therapy: preliminary results, SEVENTH EUROPEAN CONFERENCE ON CLINICAL ASPECTS AND TREATMENT OF HIV-INFECTION, 1999, pp. 87-91
SMART has been designed to study resistance among naive, responder and non
responder patients to 2 NRTIs. Responders were subjects with undetectable V
L, or a reduction > 2 Log, after greater than or equal to 6 months of thera
py. Treatment failure was defined by the detection of > 0.5 Log increase in
VL after > 6 months of therapy. Mutations were evaluated by direct sequenc
ing of the RT or by LiPA, only in patients with detectable viremia. Resista
nce to NRTIs is low among naive individuals. In non responders subjects the
re is an high rate of resistance to AZT and 3TC and a low rate of resistanc
e to ddI and d4T; this might explain the majority of treatment failures. Re
sistance to AZT and 3TC is high also in responders patients: at the moment,
our data are inadequate to evaluate whether this could impair future thera
pies or accelerate treatment failure. Resistance to d4T and ddI is low even
among non responders patients.