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. 2017 Sep 13;29(3):300–305. doi: 10.1177/0956462417730474

Table 2.

Patients who discontinued DTG/ABC/3TC.

Prior regimena Reason for switch to DTG/ABC/3TC Days on DTG/ABC/3TC Reason for DTG/ABC/3TC discontinuationb Event Subsequent regimen Returned to prior regimen AE ceased Regained/ maintained viral suppression
DTG + ABC/3TC Simplification 175 Toxicity/intolerance Headachec DTG + ABC/3TC Yes Yes Yes
ATV/r + ABC/3TC Simplification 75 Blip Single event of 63 copies/ml ATV/r + ABC/3TC Yes Yes
DTG + ABC/3TC Simplification 381 Toxicity/intolerance Creatinine EVG/c/TDF/FTC No No Yes
ATV/r + TDF/FTC Simplification 82 Toxicity/intolerance Abdominal discomfort ATV/r + TDF/FTC Yes Yes Yes
RAL + ABC/3TC Simplification 126 Toxicity/intolerance Insomnia RAL + ABC/3TC Yes Yes Yes
NVP + TDF/FTCd Toxicity/intolerance 75 Toxicity/intolerance Anxietye NVP + TDF/FTC Yes Yes Yes
RAL + ABC/3TCd Toxicity/intolerance 169 Toxicity/intolerance Dry mouth RAL + ABC/3TC Yes Yes Yes
RAL + TDF/FTC Simplification 27 Toxicity/intolerance Rash RAL + TDF/FTC Yes Yes Yes
DTG + ABC/3TC Simplification 43 Drug–drug interactions Cigarettes and risk of CVD ATV/r + TDF/FTC No Yes
DTG + ABC/3TCf Patient preference 304 Toxicity/intolerance Malaiseg NVP + ABC/3TC No Yes Yes
NVP + ABC/3TC Simplification 199 Patient preference NVP + ABC/3TC Yes Yes
DTG + ABC/3TC Simplification 345 Toxicity/intolerance Anxiety DRV/r + ABC/3TC No Yes Yes
RAL + DRV/r + ABC/3TC Simplification 186 Toxicity/intolerance Rhabdomyolysish RPV/TDF/FTC No Yes Yes
RAL + NVP + 3TC Simplification 21 Toxicity/intolerance Nausea RAL + NVP + 3TC Yes Yes Yes

3TC: lamivudine; ABC: abacavir; AE: adverse event; ATV/r: atazanavir/ritonavir; c: cobicistat; CVD: cardiovascular disease; DRV/r: darunavir/ritonavir; DTG: dolutegravir; EVG: elvitegravir; NVP: nevirapine; RAL: raltegravir; RPV: rilpivirine; TDF/FTC: tenofovir/emtricitabine.

aSwitched from prior regimens for simplification, with three exceptions.

bMedian time on DTG/ABC/3TC treatment was 147.5 (IQR 75–195.75) days in these patients.

cThis subject was entered two days after study closure.

dDiscontinued prior regimen due to a pre-existing toxicity/intolerance.

eHistory of anxiety.

fDiscontinued prior regimen due to patient preference.

gAches, shortness of breath, tight chest, coughing, fatigue.

hSerious AE: onset bilateral arms, required hospitalisation.