Abstract P122 – Table 1. Characteristics of the 14 participants with loss of virological suppression by week 48. | |||||||||
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P | Age | Gender/ethnicity | cART directly prior to baseline | RAMs prior to baseline | VL at baseline (copies/mL) | Number of viral blips prior to LVS (copies/mL) | Time to LVS (weeks) | VL at time of LVS (copies/mL) | RAMs at LVS |
1 | 51 | M/C | DRV/c/FTC/TAF | NDA | 101 | Once; 168 | 36 | 218 | NDA |
2 | 34 | F/SSA | FTC/TAF + NVP | NDA | <50 | None | 48 | 397 | NRTI: 67N, 70R, 184V |
3 | 27 | M/SSA | DTG/ABC/3TC | NDA | 15 300 | None | 48 | 1188 | None |
4 | 22 | M/SSA | Naïve | None | <50 | None | 48 | 588 000 | NDA |
5 | 33 | F/SSA | DRV/c/FTC/TAF | None | 1080 | None | 48 | 21 000 | NDA |
6 | 46 | F/C | DTG/ABC/3TC | NDA | 12 600 | None | 16 | 418 | None |
7 | 45 | M/SSA | DRV/c/FTC/TAF | None | <50 | None | 27 | 385 | NDA |
8 | 55 | F/SSA | ABC/3TC + DRV/r | NRTI: 184V INSTI: 66A, 92G | <50 | None | 32 | 578 | NDA |
9 | 51 | M/SSA | Naïve | None | 5152 | None | 17 | 2154 | None |
10 | 55 | M/SSA | DTG + FTC/TAF | None | <50 | Once; 77 | 37 | 457 | None |
11 | 31 | M/C | Naïve | None | 30 233 | None | 42 | 11 130 | NDA |
12 | 52 | M/C | DTG + FTC/TAF | None | <50 | None | 48 | 22 700 | None |
13 | 34 | M/SSA | DRV/c/FTC/TAF | None | <50 | None | 48 | 89 200 | None |
14 | 42 | M/SSA | Naïve | None | 932 | Once; 182 | 48 | 836 | NRTI: 184V INSTI: 263K/R |
ABC/3TC, abacavir/lamivudine; C, Caucasian; cART, combined antiretroviral therapy; DRV/c, darunavir/cobicistat; DRV/r, darunavir/ritonavir; DTG, dolutegravir; F, female; FTC/TAF, emtricitabine/tenofovir alafenamide; INSTI, integrase strand transfer inhibitor; LVS, loss of virological suppression; M, male; NDA, no data available; NRTI, nucleoside/nucleotide reverse transcriptase inhibitor; NVP, nevirapine; P, patient; RAMs, resistance‐associated mutations; SSA, black sub‐Saharan African; VL, viral load.