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13th Annual Conference of the British HIV Association29 March–1 April 2007, Brighton, UK |
INTER-INDIVIDUAL VARIABILITY OF ONCE DAILY BOOSTED SAQUINAVIR (SQV/r) (INVIRASE®) IN 18 HIV-1-INFECTED PATIENTS ON HIGHLY ACTIVE ANTIRETROVIRAL THERAPY (HAART)
HIV Med 2007; 8(Suppl. 1):13 (abstract no. P13)
Chinyere Okoli, David Ladenheim, Rajesh Varma and Chloe Orkin
Barts and The London NHS Trust, London, UK
AIMS: Illustrate inter-patient variability with boosted 2000 mg/100 mg SQV/r in a diverse clinic population using Invirase® as part of HAART in an ethically diverse clinic cohort.
METHODS: Retrospective case note review. Patient characteristic, disease stage, treatment history, CDC stage, BMI, CD4 count, HIV-1 viral load (VL), concurrent medication noted and trough concentration (Ctrough) from therapeutic drug monitoring (TDM) were recorded as part of routine clinical care using high performance liquid chromatography (HPLC) with patients on saquinavir/ ritonavir 2000 mg/100 mg od.
RESULTS: 18 patients identified, six (34%) protease inhibitor-naïve. Seven (39%) patients produced levels more than 10 times above minimum Ctrough recommended for wild type (wt) virus (100 ng/mL). Three (17%) patients were below the minimum Ctrough. 1/3 patients had detectable viraemia. Two (11%) patients reported adverse effects. Both were Black African women whose levels were 10 times above (Ctrough). These patients were subsequently reduced to 1500 mg/100 mg od to good clinical effect (levels remained within therapeutic range).
| Serum range (100 ng/mL for wt virus) | Number of patients |
| <100 ng/mL | 3 |
| 100–500 ng/mL | 4 |
| 500–1000 ng/mL | 4 |
| >1000 ng/mL | 7 |
DISCUSSION: This study highlights the large inter-patient variability in once daily dosing saquinavir in an ethnically diverse cohort. Further detailed pharmacokinetic studies are warranted both to establish the long-term effects of elevated SQV/r levels and the efficacy of lowering the SQV/r dose based on TDM in PI experienced patients.
2007-03-29
P13
Copyright © 2007 - British HIV Association (BHIVA) Reproduction of this abstract (other than one copy for personal reference) must be cleared through the BHIVA Organising Secretariat 1 Mountview Court, 310 Friern Barnet Lane, London N20 0LD