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TABLE 1.

Baseline characteristics of the patients participating in the ANRS 104 Study. Patients from group 1 started with amprenavir/ritonavir for the first 2 weeks and patients from group 2 started with lopinavir/r

Parameters Group 1, amprenavir n=14 Group 2, lopinavir n=23
Median age, years (range) 47 (32–53) 41 (27–65)
Males, n (%) 12 (86) 21 (91)

CDC clinical stage, n (%) n (%)
A 6 (42) 10 (43)
B 4 (29) 3 (13)
C 4 (29) 10 (43)

Median CD4+ cells/mm3 (range) 195 (65–385) 185 (3–509)

Median HIV1-RNA, log10 copies/mL (range) 4.9 (3.6–5.7) 4.6 (3.8–5.6)
Median number of previous antiretrovirals (range) 7.5 (4–12) 7.5 (4–12)
Median number of antiretrovirals taken prior to inclusion and still in use at inclusion (range) 9.5 (7–13) 10 (8–13)

Genotypic resistance n (%) n (%)
Amprenavir/r 7 (50) 9 (56)
Lopinavir/r 7 (50) 7 (30)

Median (range) number of protease mutations 7.0 (1.0–9.0) 7.0 (1.0–10.0)

Median (range) number of reverse transcriptase mutations 6.5 (0–11.0) 7.0 (0.0–11.0)

Median (range) phenotypic resistance index
Amprenavir 2.8 (0.5–24.3) 2.5 (0.5–19.5)
Lopinavir 8.7 (0.3–84.0) 10.7 (0.2–95.3)
Antimicrob Agents Chemother. 2008 May; 52(5): 1642–6.
Published online 2008 February 19. doi: 10.1128/AAC.01314-07.