Skip to main content
. Author manuscript; available in PMC: 2016 Sep 6.
Published in final edited form as: JAMA. 2016 Jul 12;316(2):191–210. doi: 10.1001/jama.2016.8900

Table 5.

Advantages and Disadvantages of Initial Antiretroviral Therapy Options for Patients in Whom InSTIs Are Not an Optiona

Darunavir (Boosted With Cobicistat
or Ritonavir) Plus TAF/Emtricitabine,
TDF/Emtricitabine,
or Abacavir/Lamivudineb
Efavirenz/TDF/Emtricitabine Rilpivirine/TAF (or TDF)/Emtricitabine
Advantages Low risk of resistance with virologic failure,
even with intermittent adherence
High efficacy in patients with baseline HIV
RNA >100 000 copies/mL
Extensive experience in patients with
concomitant tuberculosis
Widely available globally
Lowest risk of rash among NNRTI-based
therapies
Low risk of metabolic adverse effects
Smallest tablet among single-pill regimens
Disadvantages Requires pharmacokinetic boosting;
many drug interactions
Ritonavir-boosted darunavir inferior to
raltegravir and dolutegravir in separate
comparative clinical trials37,39
Results of comparative, fully powered
studies of cobicistat-boosted darunavir
as initial therapy are not yet available
Relatively high rate of rash
No single-tablet form available with TAF
High rates of neuropsychiatric adverse effects
Increased risk of suicidality in 1 study55;
avoid in patients with history of depression
Not recommended for patients with HIV RNA
>100 000 copies/mL or CD4 cell count
<200/µL owing to increased risk of virologic
failure
Must be taken with a meal to optimize
absorption
Should not be administered with proton pump
inhibitors; stagger dosing if given with
an H2 blocker

Abbreviations: InSTI, integrase strand transfer inhibitor; NNRTI, nonnucleoside reverse transcriptase inhibitor; TAF, tenofovir alafenamide; TDF, tenofovir disoproxil fumarate.

a

Nonnucleoside reverse transcriptase inhibitor–based regimens should not be used without baseline resistance data because of the possible presence of transmitted NNRTI-resistant virus. In the rare circumstance in which maraviroc might be included in initial therapy, initiation should not occur before confirmation of CC chemokine receptor 5 tropism.

b

Cautions on the use of abacavir and TAF or TDF are described in the text.