2004
DOI: 10.1097/00126334-200404010-00003
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Clinical, Virologic, and Immunologic Response to Efavirenz-or Protease Inhibitor???Based Highly Active Antiretroviral Therapy in a Cohort of Antiretroviral-Naive Patients With Advanced HIV Infection (EfaVIP 2 Study)

Abstract: : In severely immunosuppressed, antiretroviral-naive, HIV-1-infected patients, treatment with an EFV-based regimen compared with a nonboosted PI-based regimen resulted in a superior virologic response with no difference in immunologic or clinical effectiveness.

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Cited by 56 publications
(27 citation statements)
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“…In our investigation, the mean of objects' baseline CD4 + T cell count added 114/μL and 116/μL after the therapy for 3 and 6 months respectively, which indicated that HAART was useful to reconstruct immune function. This result is also consistent with the investigative findings of other countries [12][13][14] .…”
Section: Discussionsupporting
confidence: 93%
“…In our investigation, the mean of objects' baseline CD4 + T cell count added 114/μL and 116/μL after the therapy for 3 and 6 months respectively, which indicated that HAART was useful to reconstruct immune function. This result is also consistent with the investigative findings of other countries [12][13][14] .…”
Section: Discussionsupporting
confidence: 93%
“…Concerning antiretroviral effectiveness, the percentage of patients with an HIV-1 viral load <400 copies/mL at month 12 in the group of patients receiving EFV-based HAART was similar to those reported in other studies (10,19,20). However, a recently published systematic overview whose primary goal was the comparison of the effectiveness of a three-drug combination antiretroviral therapy in treatment-naive HIVinfected persons showed a higher effectiveness (73%) on the non-nucleoside reverse transcriptase inhibitors than that observed in our study (65%) (21).…”
Section: Discussionsupporting
confidence: 87%
“…A virologic, but not immunologic, superiority has been documented for non-nucleoside reverse transcriptase inhibitors (NNRTI)-based regimens when these are compared to mostly unboosted protease inhibitor (PI)-based cART in randomized trials and retrospective cohort studies [31,32]. One randomized comparative trial performed in a naïve patient population containing a relevant proportion (about 40%) of patients with advanced HIV infection showed that lopinavir/ritonavir (LPV/r)-containing regimens were associated with a better CD4+ T cell count increase as well as with a reduced risk of resistance mutation development at treatment failure, while efavirenz-containing regimens showed more likely virologic success [33].…”
Section: Choice Of Antiretroviral Treatmentmentioning
confidence: 99%
“…While numerous data are available on the potency of regimens containing efavirenz [32,34], empirical evidence for using regimens containing nevirapine in this population is limited (B-I). Even if specific studies on a direct comparison are lacking, regimens containing non-thymidine nucleoside analogues seem to be more desirable since they are associated with a better CD4+ cells recovery (B-I).…”
Section: Choice Of Antiretroviral Treatmentmentioning
confidence: 99%