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. 2012 Jan 11;205(4):557–567. doi: 10.1093/infdis/jir821

Table 1.

Patient Characteristics

Genotypic Tests, No.a
Baseline
Follow-up
Overall
Patient ID Sex CD4 Cell Count, Cells/mm3 HIV RNA Level, log10 Copies/mL Subtype GSSb Therapy With Raltegravir HIV RNA <50 Copies/mL at 24 wk UDPS Popc UDPS Popc UDPS Popc
12 F 24 5.1 B 0 3TC, DRV/r, T20 No 1 1 5 4 6 5
27 M 231 3.6 B 1.75 DRV/r, TDF, ETR No 1 1 1 1 2 2
49 F 21 4.5 B 2.5 DRV/r, FTC, TDF No 1 1 1 1
56 M 1 5.5 B 0 3TC, DDI, DRV/r, T20 No 1 1 1 1
69 F 328 4.4 B 0 3TC, DRV/r No 1 1 2 2 3 3
80 M 2 4.7 F ND 3TC, AZT, DRV/r No 1 1 1 1 2 2
81 M 83 5.3 B ND 3TC, ETR No 1 1 1 1 2 2
84 M 14 5.5 B 0.5 3TC, MVC, TDF No 1 1 7 4 8 5
141 M 276 4.9 B 1 3TC, AZT, DRV/r, ETR No 1 1 1 1 2 2
142 M 7 5.7 B ND DRV/r, ETR, FTC, T20, TDF No 1 1 1 1
145 M 480 5 B 0 3TC, DRV/r No 1 1 1 1 2 2
156 F 320 5.4 B 1.5 EFV, LPV/r No 1 1 1 2 1
162 M 192 5.1 B 2.5 ETR, SQV/r No 1 1 2 3 1
229 F 8 4.7 B 1.5 DRV/r, ETR, FTC, TDF No 1 1 3 2 4 3
5 F 315 5.3 F 2.5 DRV/r, ETR Yes 1 1 1 1
15 M 178 5.2 B 0 DRV/r, FTC, MVC, TDF Yes 1 1 1 1
16 M 132 4.6 B 0.5 3TC, DRV/r, TDF Yes 1 1 1 1
45 F 106 5.7 B ND 3TC, DRV/r, EFV Yes 1 1 1 1
57 M 105 5.3 B ND DRV/r, FTC, TDF Yes 1 1 1 1
58 M 563 4 B 0.75 DRV/r, FTC, TDF Yes 1 1 1 1
63 M 170 5.6 B 1.75 DRV/r, FTC, TDF Yes 1 1 1 1
151 M 207 4.7 B ND DRV/r, FTC, TDF Yes 1 1 1 1
155 M 11 5.7 B 1 ETR, T20 Yes 1 1 1 1
Total (n = 23) Median: 170 (IQR, 21–276) Median: 5.1 (IQR, 4.7–5.4) Median: 1.0 (IQR, 0–1.75) 23 23 25 16 48 40

Abbreviations: 3TC, lamivudine; AZT, zidovudine; DDI, didanosine; DRV/r, darunavir/ritonavir boosted; ETR, etravirine; FTC, emtricitabine; GSS, genotype sensitive score; HIV, human immunodeficiency virus; IQR, interquartile range; MVC, maraviroc; ND, not determined; Pop, population; SQV/r, saquinavir/ritonavir boosted; T20, enfuvirtide; TDF, tenofovir; .UDPS, Ultra-Deep-454 Pyrosequencing.

a

UDPS and population sequencing were not available for patients at failure ID49, ID56, ID142 (because with HIV-RNA levels < 500 copies/ml) and for all patients with HIV-RNA levels < 50 copies at 24 week.

b

The GSS to optimized background therapy was calculated for patients with an available protease and reverse-transcriptase sequence at raltegravir baseline, according to the coadministration of protease inhibitors, nonnucleoside reverse-transcriptase inhibitors, and nucleoside reverse-transcriptase inhibitors, obtained by using the Rega 8.02 algorithm.

c

Population sequencing.