Comparison of NRTI combos
Study 934 : ZDV/3TC vs TDF + FTC
Original article : N Engl J Med. 2006 Jan 19;354(3):251-60 - JE Gallant, J Acquir Immune Defic Syndr. 2008 Jan 1;47(1):74-8 - JR Arribas
Last update :
28/03/2014
Dr Anton Pozniak
Chelsea and Westminster Hospital
London, UK
- TDF + FTC + EFV is non inferior to ZDV/3TC + EFV
- Greater virologic response rates to TDF + FTC + EFV as compared with ZDV/3TC + EFV
–Significantly greater CD4 response with TDF + FTC
- Greater tolerability of TDF + FTC
- This study shows superior outcome in the tenofovir-emtricitabine group
- At week 144, TDF/FTC + EFV demonstrates superior durability of viral load suppression and an improved safety and morphologic profile compared with ZDV/3TC and EFV
Objectif :
- Non inferiority of TDF + FTC + EFV vs ZDV/3TC + EFV at W48: % HIV RNA < 400 c/mL, TLOVR algorithm (lower margin of the 95% CI for the difference = -13%, 85% power)
Design :
Baseline characteristics :
* Excluded from primary endpoint analysis
Note : TDF, FTC and EFV taken without regards to meals and preferably at bed time; Substitution of NVP for EFV allowed if EFV intolerance; not considered as treatment failure
Response to treatment at week 48 :
Safety and tolerability: TDF + FTC vs ZDV/3TC :
- Similar frequency of clinical adverse events grade 2 to 4 and laboratory abnormalities grade 2 to 4 in both groups, respectively 63% vs 63% and 56% vs 57%
- Significantly more discontinuations for adverse events in the ZDV/3TC group: 9% vs 4% (p = 0.02); mainly for anemia (N = 14 vs 0)
- Renal safety was similar in both groups and no patients discontinued because of renal events. Change in median GFR (MDRD) at W48 was similar in both groups (< - 1 mL/min/1.73 m2). No Fanconi’s syndrome occurred
- Mean increase significantly lower in the TDF + FTC group for total cholesterol, LDL-cholesterol and HDL-cholesterol; increase in triglycerides modest and not different between groups
- At week 48, DEXA substudy in 100 patients (no baseline evaluation): significantly less total limb fat with ZDV/3TC (mean 6.9 vs 8.9 kg; p = 0.03)
Resistance data :
- Genotypic analysis was done in patients without baseline NNRTI resistance if
- viral rebound
- consecutive HIV RNA > 400 c/mL after achieving < 400 c/mL HIV RNA > 400 c/mL at W48
- discontinuation before W48 with HIV RNA > 400 c/mL at the last visit
- Patients with baseline resistance (11 in each group) were excluded from this analysis of resistance
* 1 technical failure; ** K103N mutation developed in 21 of 25 patients
Study extended to 3 years of follow-up (W144) :
- At week 96, patients on TDF + FTC swithed to fixed-dose combination TDF/FTC
* No discontinuation for renal events