Data are presented as the estimated mean ± standard error of the mean. An analysis of variance (anova) was used to test for differences between the treatments. To test for differences in proportions between the treatments, a χ2 test was used. The proportion
of patients experiencing loss of virological response over 48 weeks was compared between study arms using Kaplan–Meier estimates and tested using the log rank statistic [as used by the US Food and Drug Administration (FDA)]. The time to loss of virological response (TLOVR) is an ITT analysis that defines response as two consecutive on-treatment measurements of HIV RNA of<50 copies/mL, achieved and maintained to week 48 without intervening discontinuation and virological rebound (two consecutive on-treatment measurements of plasma HIV RNA≥50 copies/mL or last measured plasma HIV RNA≥50 copies/mL). No OSI-744 mouse Bonferroni corrections of the α-error spending were used. For all statistical tests, statistical significance was assumed below a two-sided α level of 0.05. Statistical analyses were performed using sas version 9.1 (SAS Institute
Inc., Cary, NC, USA). This study is registered at ClinicalTrials.gov (number NCT00389402). A total of 123 HIV-1-infected, treatment-naïve patients were randomized in this study, of whom 32 were originally randomized in the SSAR 2004/0002 trial find protocol and 91 were newly randomized. Patients’ dispositions and baseline characteristics are shown in Figure 1 and Table 1. Patients were comparable between arms mafosfamide with respect to baseline demographic and HIV-disease characteristics. Insufficient baseline samples remained for centralized retesting of lipids for five SSAR 2004/0002 study participants (SQV/r arm, n=3; ATV/r arm, n=2). Thus, 113 patients (SQV/r arm, n=54; ATV/r arm, n=59) were included in the primary analysis. Absolute changes in lipids are shown in Table 2 and changes in TC in Figure 2. During 24 weeks of follow-up, TC increased significantly by +9.0 ± 2.7% in the SQV/r arm and +5.6 ± 2.3% in the ATV/r arm (difference 3.4
± 3.6%; P=0.3). HDL cholesterol increased significantly in both arms, +16.1 ± 3.8% in the SQV/r arm and +12.2 ± 3.4% in the ATV/r arm (difference 3.9 ± 5.1%; P=0.5). The TC/HDL cholesterol ratio did not change significantly in either arm. ApoA1 increased significantly in both arms, +6.0 ± 2.2% in the SQV/r arm and +6.1 ± 16.2% in the ATV/r arm (difference 0.1 ± 3.1%; P=1.0). Comparable changes in lipids were seen during further follow-up. The concentration of TC stabilized after 24 weeks, with a total increase of+8.0 ± 2.8% in the SQV/r arm and+7.2 ± 2.5% in the ATV/r arm after 48 weeks (difference 0.8 ± 3.6%; P=0.8). A significant further increase in HDL cholesterol was observed in both arms, by +26.4 ± 5.8% in the SQV/r arm and+14.8 ± 3.2% in the ATV/r arm over the whole 48 weeks (difference 11.6 ± 6.4%; P=0.07).