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Recommendation on Integrase Inhibitor Use in Antiretroviral Treatment-Naive HIV-Infected Individuals from the HHS Panel on Antiretroviral Guidelines for Adults and Adolescents

Date: October 30, 2013
Source: AIDSinfo
URL: http://aidsinfo.nih.gov/contentfiles/upload/AdultARV_INSTIRecommendations.pdf

Introduction

In the February 12, 2013, version of the Health and Human Services (HHS) Guidelines for the Use of Antiretroviral Agents in HIV-1-Infected Adults and Adolescents, the Panel recommendations on initial combination regimens for the antiretroviral therapy (ART)-naive, HIV-infected patient include raltegravir (RAL) plus tenofovir disoproxil fumarate/emtricitabine (TDF/FTC) as the preferred integrase strand transfer inhibitor (INSTI)-based regimen, and elvitegravir (EVG)/cobicistat (cobi)/TDF/FTC as an alternative regimen for patients with estimated creatinine clearance (CrCl) ≥70 mL/min. Since the release of the Guidelines, a new INSTI, dolutegravir (DTG), was approved for use in ART-naive and ART-experienced patients. Additionally, long-term follow-up data (up to 144 weeks) from randomized clinical trials have demonstrated the durable safety and efficacy of EVG/cobi/TDF/FTC.

On the basis of these new findings, the Panel now recommends the following 4 INSTI-based regimens as preferred regimens for ART-naive patients (arranged in order of drug approval):

  • Raltegravir 400 mg twice daily plus tenofovir 300 mg/emtricitabine 200 mg once daily (AI)
  • Elvitegravir 150 mg/cobicistat 150 mg/tenofovir 300 mg/emtricitabine 200 mg once daily in patients with estimated CrCl ≥70 mL/min (AI)
  • Dolutegravir 50 mg once daily plus abacavir 600 mg/lamivudine 300 mg once daily in patients who are HLA B*5701 negative (AI)
  • Dolutegravir 50 mg once daily plus tenofovir 300 mg/emtricitabine 200 mg once daily (AI)

Rationale for Upgrading Elvitegravir/Cobicistat/Tenofovir/Emtricitabine to a Preferred INSTI-Based Regimen
Since the inclusion of co-formulated EVG/cobi/TDF/FTC as an alternative INSTI in the February 2013 guidelines, 96 week data from 2 Phase 3 clinical trials have been published,1,2 and additional data through 144 weeks have been presented.3,4 In these studies, EVG/cobi/TDF/FTC remained non-inferior to co-formulated efavirenz (EFV)/TDF/FTC3 and to ritonavir-boosted atazanavir (ATV/r) plus TDF/FTC at Week 144.4 No additional occurrences of proximal renal tubulopathy were reported in the EVG/cobi/TDF/FTC-treated participants in either study beyond 24 weeks. Additionally, following early, modest increases in serum creatinine observed with EVG/cobi/TDF/FTC therapy, there were no further increases in creatinine levels through Week 144.3,4 These data, along with post marketing clinical experience with the co-formulated product, are the basis for the Panel’s decision to recommend EVG/cobi/TDF/FTC as a preferred regimen for ART-naive patients.

Dolutegravir-Based Regimens for Treatment-Naive Patients
In 3 Phase 3 randomized controlled trials, DTG 50 mg once daily plus 2 nucleoside reverse transcriptase inhibitors (NRTIs) was compared to 3 Guidelines-designated preferred regimens:

  1. DTG versus RAL, administered either with investigator-selected abacavir/lamivudine (ABC/3TC) or TDF/FTC;5
  2. DTG plus ABC/3TC versus EFV/TDF/FTC;6 and
  3. DTG versus ritonavir-boosted darunavir (DRV/r), administered either with investigator-selected ABC/3TC or TDF/FTC.7

The primary endpoint for these trials was the proportion of patients with HIV RNA <50 copies/mL at Week 48. DTG was found to be non-inferior to RAL at Week 48 and also at Week 96.5,8 DTG-based regimens were also found to be superior to DRV/r- and EFV-containing regimens, largely because of more discontinuations for adverse events or other reasons in the comparator arms. No emergent DTG resistance has been observed thus far in clinical trials of DTG in treatment-naive patients.

Overall, DTG was well tolerated in clinical trials, with insomnia and headache of moderate to severe intensity (in 3% and 2% of patients, respectively) being the most commonly reported adverse effects. Cases of hypersensitivity reaction have been reported in clinical trials. DTG decreases tubular secretion of creatinine without affecting glomerular function, with increases in serum creatinine observed within the first 4 weeks of treatment (mean change from baseline in serum creatinine of 0.11 mg/dL after 48 weeks); no discontinuations due to drug-related renal adverse events have been seen to date.9

Summary
In summary, all three approved INSTIs have been shown in randomized clinical trials to be non-inferior to other preferred ART regimens for treatment-naive patients. Each INSTI-based regimen has distinctive characteristics; certain clinically relevant features are summarized below and in Table 1.

  • Raltegravir remains a preferred INSTI because it has the longest clinical trial and post-marketing experience and has been shown to have durable potency. However, it requires twice daily dosing.
  • Elvitegravir is available as a fixed-dose combination product that is taken as a single-tablet, once-daily regimen. It must be given with food. The fixed-dose combination product includes cobi, which is a potent CYP3A4 inhibitor that may result in drug-drug interaction with other concomitant medications. Additionally, the fixed-dose combination product is only approved for patients with estimated creatinine clearance of ≥70 mL/min.
  • Dolutegravir is the most recently approved INSTI. It can be given once daily with or without food. In randomized trials, DTG was non-inferior to RAL and was superior to both DRV/r and EFV (because of fewer drug discontinuations in those who received DTG). However, DTG has the shortest duration of follow-up and limited post-marketing experience to date.

Table 1. Comparison of 4 INSTI-Based Regimens
  RAL + TDF/FTC  EVG/cobi/TDF/FTC DTG + ABC/3TC DTG + TDF/FTC
Comparators in Randomized Trials EFV/TDF/FTC  

EFV/TDF/FTC

ATV/r + TDF/FTC

 

EFV/TDF/FTC

DRV/r + 2 NRTI

RAL + 2 NRTI

 

DRV/r + 2 NRTI

RAL + 2 NRTI

 

 

 

Follow-Up Data >5 years 144 weeks 48–96 weeks 48–96 weeks

Post-Marketing Experience 6 years 1 year Minimal Minimal

Dosing Frequency

Twice daily

 

Once daily

 

Once daily

 

Once daily

 

 

 

Numbers of Tablets Per Day 3 1 2 2

Meal Consideration  None Take with a meal None None

CYP 3A4 Interactions No Yes
• cobi—potent CYP3A4 inhibitor
• EVG—CYP3A4 substrate
No
• DTG—minor CYP3A4 substrate
No
• DTG–minor CYP3A4 substrate

CrCl and Dosing Dosage adjustment for TDF and FTC if CrCl <50 mL/min Not recommended if
CrCl <70 mL/min
Dosage adjustment for 3TC if
CrCl <50 mL/min
Dosage adjustment for TDF and FTC if CrCl <50 mL/min

HLA B*5701 (+) Patients

No concern

 

No concern

 

Do not use this regimen.

 

No concern

 

 

 

Key to Acronyms: 3TC = lamivudine; ABC = abacavir; ATV/r = atazanavir/ritonavir; cobi = cobicistat; CrCl = creatinine clearance; DRV/r = ritonavir-boosted darunavir; DTG = dolutegravir; EFV = efavirenz; EVG = elvitegravir; FTC = emtricitabine; INSTI = integrase strand transfer inhibitor; NRTI = nucleoside reverse transcriptase inhibitor; RAL = raltegravir; TDF = tenofovir disoproxil fumarate

References

  1. Rockstroh JK, DeJesus E, Henry K, et al. A randomized, double-blind comparison of coformulated elvitegravir/cobicistat/emtricitabine/tenofovir DF vs ritonavir-boosted atazanavir plus coformulated emtricitabine and tenofovir DF for initial treatment of HIV-1 infection: analysis of week 96 results. J Acquir Immune Defic Syndr. Apr 15 2013;62(5):483-486. Available at http://www.ncbi.nlm.nih.gov/pubmed/23337366.
  2. Zolopa A, Sax PE, DeJesus E, et al. A randomized double-blind comparison of coformulated elvitegravir/cobicistat/emtricitabine/tenofovir disoproxil fumarate versus efavirenz/emtricitabine/tenofovir disoproxil fumarate for initial treatment of HIV-1 infection: analysis of week 96 results. J Acquir Immune Defic Syndr. May 1 2013;63(1):96-100. Available at http://www.ncbi.nlm.nih.gov/pubmed/23392460.
  3. Wohl D, Cohen D, Gallant J, et al. Elvitegravir/cobicistat/emtricitabine/tenofovir DF (STB) has durable efficacy and differentiated long-term safety and tolerability versus efavirez/emtricitabine/tenofovir DF (ATR) at week 144 in treatment-naïve HIV patients. Paper presented at: 53rd Interscience Conference on Antimicrobial Agents and Chemotherapy; Sep 10–13, 2013; Denver, CO. Abstract H-672a.
  4. Clumeck N, Molina J, Henry K, Gathe J, et al. Elvitegravir/Cobicistat/Emtricitabine/Tenofovir DF (STB) has durable efficacy and differentiated safety compared to atazanavir boosted by ritonavir plus emtricitabine/tenofovir DF at week 144 in treatment-naïve HIV-1 infected patients. Paper presented at: 14th European AIDS Conference. October 16-19, 2013. Brussels, Belgium. Abs LBPS7/2.
  5. Raffi F, Jaeger H, Quiros-Roldan E, et al. Once-daily dolutegravir versus twice-daily raltegravir in antiretroviral-naive adults with HIV-1 infection (SPRING-2 study): 96 week results from a randomised, double-blind, non-inferiority trial. Lancet Infect Dis. Nov 2013;13(11):927-935. Available at http://www.ncbi.nlm.nih.gov/pubmed/24074642.
  6. Walmsley S, Antela A, Clumeck N, et al. Dolutegravir (TDG: S/GSK11349572) + abacavir/lamivudine once daily statistically superior to tenofovir/emtricitabine/efavirenz: 48-week results—SINGLE (ING114467). Paper presented at: 52nd Interscience Conference on Antimicrobial Agents and Chemotherapy. Sep 9–12, 2012, San Francisco.
  7. Feinberg J, Clotet B, Khuong-Josses MA, al. E. Once-daily dolutegravir (DTG) is superior to darunavir/ritonavir (DRV/r) in antiretroviral-naïve adults: 48 week results from FLAMINGO (ING114915). Paper presented at: 53rd Interscience Conference on Antimicrobial Agents and Chemotherapy; Sep 10–13, 2013; Denver, CO.
  8. Raffi F, Rachlis A, Stellbrink HJ, et al. Once-daily dolutegravir versus raltegravir in antiretroviral-naive adults with HIV-1 infection: 48 week results from the randomised, double-blind, non-inferiority SPRING-2 study. Lancet. Mar 2 2013;381(9868):735-743. Available at http://www.ncbi.nlm.nih.gov/pubmed/23306000.
  9. Food and Drug Administration. Tivicay (package insert). http://www.accessdata.fda.gov/drugsatfda_docs/label/2013/204790lbl.pdf. Accessed October 28, 2013.