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Changes in Lipids in Randomised, Open-Label Comparative Trial of Abacavir or Tenofovir DF as Replacement for a Thymidine Analogue in Persons with Lipoatrophy.

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Presentation on theme: "Changes in Lipids in Randomised, Open-Label Comparative Trial of Abacavir or Tenofovir DF as Replacement for a Thymidine Analogue in Persons with Lipoatrophy."— Presentation transcript:

1 Changes in Lipids in Randomised, Open-Label Comparative Trial of Abacavir or Tenofovir DF as Replacement for a Thymidine Analogue in Persons with Lipoatrophy and Suppressed HIV RNA on HAART The RAVE Study ICAAC 2005 G Moyle 1, C Sabin 2, J Cartledge 3, M Johnson 2, E Wilkins 4, D Churchill 5, P Hay 6, A Fakoya 7, M Murphy 8, G Scullard 9, C Leen 10, G Reilly 11 for the RAVE study group UK 1 Chelsea and Westminster Hosp, London, 2 Royal Free & UC Medical School, London, 3 UCL London, 4 North Manchester Hosp, 5 Lawson Unit Royal Sussex County Hosp, 6 St Georges Hosp London, 7 Newham General London, 8 St Barts & The London, 9 St Mary’s Hosp London, 10 Western General Hosp Edinburgh, 11 Gilead Sciences UK

2 RAVE Rationale  Thymidine analogue therapy is associated with peripheral fat loss and dyslipidemia  Duration of exposure to HAART has been associated with increased risk of CV disease. This may, in part, be mediated through ART-associated dyslipidemia  In initial treatment regimens tenofovir is associated with smaller changes in total cholesterol and triglycerides than either d4T or AZT  The lipid profile of abacavir relative to thymidine analogues has not been well characterised Moyle et al. 45 th ICAAC Sept 21-24, 2005: abstract H-340

3 RAVE Design Thymidine analogue recipients (n = 105) randomised 1:1 48 wks Moderate-Severe Lipoatrophy Any CD4 cell count HIV RNA <50 c/mL Stable ARV Therapy for >24 weeks TDFQD + NRTI + PI, PI/r or NNRTI No history of TDF or ABC use or resistance Adequate Renal and Hepatic Function at baseline ABCBD + NRTI + PI, PI/r or NNRTI Moyle 12 th CROI 2005: 44LB

4 RAVE Statistical Methods  Trial endpoints: change in total limb fat mass (by DEXA) and lipids from baseline to 48 weeks  Changes in lipids were approximately normally distributed  Changes in values over 48 weeks were tested for significance using paired t-tests; the changes in the two treatment groups were compared using unpaired t-tests  Analyses of changes in lipids were based on all values as measured, disregarding any information on the use of lipid-lowering therapy  All analyses were performed on an intention-to-treat basis. Missing values were imputed using a last- observation-carried-forward approach Moyle et al. 45 th ICAAC Sept 21-24, 2005: abstract H-340

5 RAVE Baseline Characteristics TDF (n=52) ABC (n=53) Male sex:94%87% White race:85%83% Median age (years):4243 Nadir CD4 (median, IQR):114 (0, 818)154 (2, 783) Current CD4 (median, IQR):522 (314, 724)478 (340, 653) Years on ART (median, IQR): Current PI-sparing regimen 5.7 (0.8, 11.5) 63% 4.9 (0.8, 8.1) 74% Current thymidine analogue: d4T77%59% AZT23%41% Moyle et al. 45 th ICAAC Sept 21-24, 2005: abstract H-340

6 RAVE Baseline Median Metabolics TDF (n=52) ABC (n=53) Total Cholesterol (mmol/l)5.65.3 HDL-C (mmol/l)1.3 LDL-C (mmol/l)3.33.0 Triglycerides (mmol/l)2.01.7 Insulin (IU/l) Fasting Glucose (mmol/l) 8.8 5.1 7.2 5.2 Lactate (mmol/l)1.51.3 Moyle et al. 45 th ICAAC Sept 21-24, 2005: abstract H-340

7 RAVE Patient Disposition through Week 48 TDF (n=52) ABC (n=53) N (%) discontinued study3 (6%)8 (15%) - Lost to follow-up-1 (2%) - Patient withdrew consent1 (2%)2 (4%) - Protocol violation-2 (4%) - Adverse event1 (2%)3 (6%)* - Other1 (2%)- Median time to discontinuation (weeks, range) 36 (4, 39)19 (1.6, 40) * All discontinuations due to adverse events in ABC group were due to hypersensitivity reaction, TDF related discontinuation was secondary to diarrhoea Moyle et al. 45 th ICAAC Sept 21-24, 2005: abstract H-340

8 RAVE Median Change in Limb Fat DEXA arm fat + total leg fat in grams (ITT m=f analysis) Median Baseline Limb Fat TDF 3.0kg, ABC 2.9kg Moyle 12 th CROI 2005: 44LB p=0.97

9 RAVE Median changes at week 48 in Limb Fat by DEXA by baseline characteristics p=0.97 Change in fat mass (g) by DEXA Moyle 12 th CROI 2005: 44LB n: 49 44 12 16 37 28 31 32 18 12 Median Baseline Limb Fat 3.0kg 2.9kg2.91kg 2.74kg5.12kg 2.97kg

10 RAVE Mean Change in Metabolic Outcomes to Week 48 *P values by paired t- test P=0.71 P=0.003 P=0.12 P=0.04P=0.34 LactateTotal Cholesterol HDL Cholesterol LDL Cholesterol Triglycerides All individuals included. Lipid lowering therapy commenced during study for TDF n=1, at 273 days, ABC n=8, at median 91.5days Includes fasting and non-fasting samples. Observations are similar when only fasting samples are included Moyle et al. 45 th ICAAC Sept 21-24, 2005: abstract H-340

11 RAVE Changes in Mean Fasting Cholesterol (mmol/l) by baseline Thymidine analog Fasting Cholesterol (mmol/l) d4T at BaselineAZT at Baseline Moyle et al. 45 th ICAAC Sept 21-24, 2005: abstract H-340

12 RAVE Changes in Mean Fasting LDL-c (mmol/l) by baseline thymidine analogue Fasting Cholesterol (mmol/l) AZT at Baselined4T at Baseline Moyle et al. 45 th ICAAC Sept 21-24, 2005: abstract H-340

13 RAVE Changes in Mean Fasting HDL-c (mmol/l) by baseline Thymidine analogue Fasting Cholesterol (mmol/l) d4T at BaselineAZT at Baseline Moyle et al. 45 th ICAAC Sept 21-24, 2005: abstract H-340

14 RAVE Changes in Mean Fasting Triglycerides (mmol/l) by baseline Thymidine analogue Fasting Cholesterol (mmol/l) d4T at BaselineAZT at Baseline All data LOCF. All individuals included. Lipid lowering therapy commenced during study for TDF n=1, at 273 days, ABC n=8, at median 91.5days Includes fasting and non-fasting samples. Observations are similar when only fasting samples are included Moyle et al. 45 th ICAAC Sept 21-24, 2005: abstract H-340

15 RAVE: % patients with dyslipidemia* at baseline and week 48 by randomized group Baseline P=0.24 P=1.00 Total Cholesterol >6.2mmol/l or 240mg/dl HDL Cholesterol <0.9mmol/l or 35mg/dl Week 48 Baseline Week 48 * NCEP ATPIII Category ‘high’ Moyle et al. 45 th ICAAC Sept 21-24, 2005: abstract H-340 Baseline Week 48 Baseline Week 48 LDL Cholesterol >4.1mmol/l or 160mg/dl Triglycerides <2.3mmol/l or 200mg/dl P=1.00

16  TDF and ABC similarly allow restoration of limb fat over 48 weeks when switching from thymidine analogues in persons with lipoatrophy  Lipid changes favored the TDF arm. Fewer TDF patients initiated lipid lowering therapy  Baseline lipids were generally higher in the d4T arm  Falls in total cholesterol and TGs were predominately seen in individuals on d4T at baseline RAVE Summary Moyle et al. 45 th ICAAC Sept 21-24, 2005: abstract H-340


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