IAS 2013: Study Supports WHO Second-line HIV Treatment Guidelines for Resource-limited Countries


A second-line regimen consisting of a protease inhibitor (PI) plus 2 nucleoside/nucleotide reverse transcriptase inhibitors (NRTIs) led to good outcomes for people with HIV in Africa after initial regimen failure, according to data from the EARNEST study presented at the 7th International AIDS Society Conference on HIV Pathogenesis, Treatment and Prevention (IAS 2013) this week in Kuala Lumpur. A NRTI-sparing regimen with raltegravir did not work significantly better, and PImonotherapy was inferior.

Large-scale roll-out of antiretroviral therapy (ART) in resource-limited settings often relies on a public health approach using standardized regimens and basic monitoring tools. While this works well for first-line treatment, the picture is more complicated for second-line therapy due to issues such as drug resistance.

Individualized therapy is hampered by limited availability of viral load and resistance testing, making it difficult to determine whether the remaining antiviral potency of previously used NRTIs outweighs their toxicity. Some research indicates that omitting NRTIs can reduce regimen complexity, cost, and side effects without compromising efficacy.

Nicholas Paton and fellow investigators with the EARNEST (Europe-Africa Research Network for Evaluation of Second-line Therapy) trial compared 3 second-line strategies for patients who experienced first-line treatment failure:

This open-label study included 1277 patients in 5 African countries who experienced failure of their first-line treatment. Failure was defined, using WHO criteria, based on high viral load or low CD4 cell count with viral load confirmation.

About 60% of study participants were women, the median age was 37 years, and they had been on ART for 4 years on average. They had a low baseline CD4 count of approximately 70 cells/mm3 at the time of randomization and an even lower CD4 nadir of about 60 cells/mm3. About 40% had high viral load (>100,000 copies/mL) at baseline.

Participants were randomly assigned (1:1:1) to one of the 3 study arms and followed for 144 weeks between April 2010 and April 2011. Almost everyone used lopinavir/ritonavir (Kaletra or Aluvia) as their PI and 80% included tenofovir (Viread) as one of their NRTIs (70% in combination with emtricitabine [Zerit]).

The study used a composite endpoint of "good HIV disease control" that combined survival, absence of AIDS events, CD4 count >250 cells/mm3, and either viral load <10,000 copies/mL or a higher viral load without PI resistance mutations at 96 weeks.

The researchers hypothesized that the raltegravir-containing regimen would demonstrate superior efficacy compared with PI/NRTI combinations, while PI monotherapy would be non-inferior.


The researchers concluded that the PI/NRTI strategy led to "excellent clinical outcome" and viral suppression -- even for patients with advanced first-line treatment failure, and without using resistance testing or viral load monitoring -- and "should be made more widely available for second-line therapy."

PI monotherapy, they continued, is inferior to PI/NRTI, with lower viral load suppression and more resistance, and is "unsuitable for [a] public health approach."

The EARNEST results provide a "strong endorsement of WHO recommendations," Paton said. It was a surprise, he added, that recycled NRTIs appear to retain substantial antiviral efficacy with little added toxicity.

SEE ALSO: Second-line Therapy in Resource-limited Settings [VIDEO]



N Paton, C Kityo, A Hoppe, et al. A pragmatic randomised controlled strategy trial of three second-line treatment options for use in public health rollout programme settings: the Europe-Africa Research Network for Evaluation of Second-line Therapy (EARNEST) Trial. 7th International AIDS Society Conference on HIV Pathogenesis, Treatment and Prevention (IAS 2013). Kuala Lumpur, June 30-July 3, 2013. Abstract WELBB02.