Index - 6 - 7 - 8/9 - 10/11/12 - 13 - 14 - 15 - 16 - 17 - 18/19 - 20/21 - 22/23

INITIAL COMBINATION REGIMEN FOR ANTIRETROVIRAL-NAÏVE PATIENT
Select 1 drug in column A and 1 NRTI combination in column B A B

Remarks

Recommended

NNRTI

  • EFV 1
  • NVP 5

 

or ritonavir-
boosted PI
  • ATV/r 6
  • DRV/r 6
  • LPV/r 7
  • SQV/r
TDF/FTC
ABC/3TC 2-3-4
  • TDF/FTC co-formulated
  • ABC/3TC co-formulated
  • EFV/TDF/FTC co-formulated
  • ATV/r: 300/100 mg qd
  • DRV/r: 800/100 mg qd
  • LPV/r:400/100 mg bid or 800/200 mg qd
  • SQV/r:1000/100 mg bid
Alternative

SQV/r
FPV/r

RAL 9

  • ZDV/3TC 8
  • ddI/3TC or FTC 8
  • SQV/r: 2000/100 mg qd
  • FPV/r:700/100 mg bid or 1400/200 mg qd
  • RAL: 400 mg bid
  • ZDV/3TC co-formulated
  1. EFV: not recommended in pregnant women or women with no reliable and consistent contraception; not active on HIV-2 and HIV-1 group O
  2. Contra-indicated if HLA B*5701 positive. Even if HLA B*5701 negative, counselling on HSR risk still mandatory
  3. ABC + NVP contra-indicated, unless HLA B*5701 negative
  4. Abacavir should be used with caution in patients with a high cardiovascular risk and/or patients with a viral load higher than 100,000 copies/ml.
  5. NVP: Use with extreme caution in women with CD4 >250 and men with CD4 >400/μL; not active on HIV-2 and HIV-1 group O
  6. Castle study (LPV/r vs ATV/r) has shown better tolerability of ATV/r and Artemis study (LPV/r vs DRV/r) better efficacy and greater tolerability of DRV/r.
  7. ACTG 5142, randomised study showed lower virological efficacy of LPV/r vs EFV. However no PI mutations were seen in the LPV/r failures.
  8. Only if unavailable or intolerant to other recommended NRTIs
  9. Raltegravir is indicated in combination with other anti-retroviral medicinal products for the treatment HIV-1 infection in adult patients. It has been studied only in combination with TDF/FTC in naïve patients with limited follow-up (48 weeks).