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. 2021 Apr 9;35(9):1333–1342. doi: 10.1097/QAD.0000000000002883

Table 2.

Multivariable logistic regression analysis of confirmed virologic failure through Week 48.

N Parameter Full model OR (95% CI), Pa Backwards elimination model OR (95% CI), Pa
1039 RPV RAM(s) at baseline 30.23 (6.25–>99), <0.001 40.36 (8.81–>99), <0.001
Log2 of post hoc Week 8 RPV trough concentration 3.85 (1.15–14.29)b, 0.029 5.00 (1.79–16.67)b, 0.002
Baseline HIV-1 subtype A6/A1 2.37 (0.34–22.14), 0.394 5.92 (1.62–22.89), 0.008
BMI (kg/m2) at baseline 1.08 (0.96–1.22), 0.192 1.13 (1.02–1.24), 0.020
Prespecified INSTI polymorphism (excluding L74I [excluding mixtures with L74M]) at baseline 0.16 (0.01–1.05), 0.057 0.14 (0.01–0.91), 0.038
NNRTI RAM(s) (excluding RPV RAMs) at baseline 2.64 (0.72–9.21), 0.137 2.78 (0.78–9.63), 0.111
Q8W regimen 2.76 (0.65–11.68), 0.164 2.77 (0.67–11.38), 0.156
L74I (excluding mixtures with L74M) INSTI polymorphism at baseline 2.51 (0.33–13.85), 0.347 Eliminated from model
Female (sex at birth) 1.09 (0.26–4.36), 0.899 Eliminated from model
Log2 of post hoc Week 8 CAB trough concentration 0.66 (0.25–1.74), 0.395 Eliminated from model

CAB, cabotegravir; CI, confidence interval; INSTI, integrase strand transfer inhibitor; NNRTI, nonnucleoside reverse transcriptase inhibitor; OR, odds ratio; Q8W, every 8 weeks; RAM, resistance-associated mutation; RPV, rilpivirine.

a

95% penalized profile confidence intervals and penalized likelihood ratio P values are provided. Backwards elimination used a significance threshold of alpha = 0.2. CAB and RPV pharmacokinetic parameters were log2-transformed; therefore, the corresponding odds ratios are per halving of each variable.

b

Results are reciprocal of these so that all ORs are in same direction.