Ninth International Congress on Drug Therapy in HIV Infection Glasgow, UK - 9-13 November 2008

J Int AIDS Soc 2008, 11(Suppl 1):18 doi:10.1186/1758-2652-11-S1-O18

F Maggiolo¹, M Airoldi¹, A Callegaro¹, C Martinelli², A Dolara³, T Bini⁴, G Gregis¹, P Quinzan¹, V Ravasio¹ and F Suter^1
1 Ospedali Riuniti, Bergamo, Italy ² Ospedale Careggi, Firenze, Italy ³ Ospedale San Gerardo, Monza, Italy ⁴ Ospedale San Paolo, Milano, Italy

PURPOSE OF THE STUDY: To compare continuous HAART with a CD4-driven STI strategy.

METHODS: LOTTI is a randomized, controlled, prospective trial. Patients with HIV-RNA < 50 copies/ml and CD4 counts >700 cells/ mcL were randomised to continue HAART or to stop it; 350 cells/mcL was the immunologic threshold to resume HAART. The primary endpoint is clinical: development of any opportunistic disease, death from any cause, or the occurrence of diseases, other than opportunistic, requiring hospital admission. Secondary end-points are major adverse effects, virologic failures and therapeutic costs. An interim ITTanalysis at 4-years follow-up is presented.

SUMMARY OF RESULTS: 329 patients were randomized. The total follow-up time is 1,388 person-years. Patients in the STI group performed a total of 241 STI cycles. On average, patients in the STI group were on HAART for 34.7% (mean 515 days) of follow-up time, in the control group this value raised to 98.3% (mean 1,530 days). The primary end point of the study occurred in 12.1% of patients on STI and in 11.6% of controls (OR 1.05; 95% CI 0.5–2.1). The 95% CI for the difference between groups was far below the pre-defined 12% limit assumed to define equivalence. Resistance-conferring mutations were selected in 4.8% of STI patients and in 6.7% of controls (OR 0.79; 95% CI 0.3–1.8). Grade 3 or 4 adverse events were observed in 27.4% of controls and only in 20.6% of patients in the STI group. The mean daily total cost for controls was 20.29 euros and it dropped to 9.07 euros in the STI arm (p < 0.0001).

CONCLUSION: CD4-guided STIs may be a possible alternative strategic option for chronically infected individuals responding to HAART provided that CD4 decrements would be steadily maintained above a safe threshold. STIs warrant further careful prospective evaluation especially to investigate virologic and clinical outcomes in the very long period.

2008-11-10
1758-2652-11-S1-O18

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