IAS 2009: Lipid and Glucose Changes Related to Boosted Darunavir (Prezista) in Children and Adolescents with HIV: DELPHI Study

Ritonavir-boosted darunavir (Prezista) was effective and generally well-tolerated at week 48 among treatment-experienced children and adolescents with HIV in the DELPHI study, according to a presentation at the 5th International AIDS Society Conference on HIV Pathogenesis, Treatment, and Prevention (IAS 2009) last month in Cape Town, South Africa. No change was seen in glucose levels after starting the drug, and triglyceride levels decreased significantly.

The Phase 2, open-label DELPHI (Darunavir EvaLuation in Pediatric HIV-1-Infected) trial included 80 pediatric HIV patients aged 6-17 years; 71% were male and 78% had been infected via mother-to-child transmission. At baseline, the average CD4 cell count was 330 cells/mm3 and the average CD4 percentage was 17%. Patients were highly treatment experienced, with all having used at least 2 NRTIs, 79% having used NNRTIs, and 96% having used protease inhibitors.

Participants received twice-daily darunavir/ritonavir dosed according to weight (11-19 mg/kg) plus an optimized background regimen containing at least 2 other antiretroviral drugs.

As previously reported, at 48 weeks, 48% of participants had HIV RNA < 50 copies/mL, 59% had viral load < 400 copies/mL, and 65% experienced at least a 1 log decrease in HIV RNA. Darunavir/ritonavir was generally well-tolerated and had a good safety profile.

In the present analysis, the investigators looked specifically at metabolic changes after starting darunavir/ritonavir. Participants were not permitted to use lipid-lowering agents to manage elevated cholesterol or triglycerides. Blood samples were collected at baseline and week 48 after patients had fasted for at least 10 hours.


"Darunavir/ritonavir has a favorable lipid and glucose safety profile in treatment-experienced, HIV-1-infected pediatric patients," the DELPHI investigators concluded.

"The most frequent laboratory abnormalities were increased total cholesterol and LDL," they continued. "The most pronounced change was a significant reduction in mean triglycerides from baseline to Week 48."

"Small but statistically significant mean increases in total cholesterol, LDL, and HDL were observed," they noted. However, "no statistically significant changes in total cholesterol/HDL ratio and mean glucose were seen."

Chris Hani Baragwanath Hospital, University of the Witwatersrand, Johannesburg, South Africa; Hospital Dos Servidores Do Estado, Rio De Janeiro, Brazil; Hospital Geral De Nova Iguacu - HGNI DST/AIDS, Nova Iguacu, Brazil; Universidade Federal De Minas Gerais, Belo Horizonte, Brazil; Tibotec BVBA, Mechelen, Belgium; Hôpital Necker Enfants Malades, Paris, France.



T Meyers, E Joao, JH Pilotto, and others. 48-week lipid- and glucose-related safety profile of darunavir/ritonavir in treatment-experienced, paediatric patients in DELPHI. 5th International AIDS Society Conference on HIV Pathogenesis, Treatment, and Prevention (IAS 2009).July 19-22, 2009. Cape Town, South Africa. Abstract TUAB202.