Naive* patients Experienced patients
  Without
co-infection
(N=195)
With
co-infection
(N=61)
p** Without
co-infection
(N=624)
With
co-infection
(N=399)
p**
FPV/r discontinuation
  110 (56.4%) 40 (65.6%) 0.20** 359 (57.5%) 223 (55.9%) 0.60**
Discontinuation reasons
Intolerance 30 (15.4%)  16(26.2%) 0.55 123 (19.7%) 64 (16.0%) ***
Simplification 33 (16.9%) 9(14.8%)   41 (6.6%) 15(3.8%)  
Death 3(1.5%) 0(0%)   1 (0.2%) 8(2.0%)  
Immuno-virological failure 19(9.7%) 5(8.2%)   107 (17.1%) 58(14.5%)  
Other*** 25(12.8%) 10(16.4%)   87(13.9%) 78(19.5%)  
Reasons for FPV/r discontinuation due to intolerance
Digestive side effects 12 (6.2%) 10 (16.4%)   51 (8.2%) 18 (4.5%)  
Biological toxicity**** 6 (3.1%) 1 (1.6%)   15 (2.4%)  7 (1.8%)  
Lipodystrophy 4 (2.1%) 0 (0%)   10 (1.6%)  4 (1.0%)  
Drug intolerance / toxicity 4 (2.1%) 1(1.6%)   10 (1.6%)  8 (2.0%)  
Cutaneous side effects /HSR 1(0,5%) 2 (3.2%)   15 (2.4%)  7 (1.8%)  
Liver toxicity 1(0.5%) 1 (1.6%)    1 (0.2%)  9 (2.2%)  
Neuro-/psychiatric side effects 0(0%) 0 (0%)    6 (1.0%)  1 (0.3%)  
Cardiovascular side effects 0(0%) 0(0%)    0(0%) 3(0.8%)  
Musculoskeletal side effects /myositis 0(0%) 0(0%)    3(0.5%) 0(0%)  
Renal side effects 0(0%) 0(0%)    1(0.2%) 0(0%)  
Other side effects 2(1.0%) 1(1.6%)   11(1.8%) 7(1.8%)  
Table 2: Discontinuation rate and reasons for FPV/r discontinuation according to the absence or presence of HCV and/or HBV co-infection. * ”naïve patients”: FPV/r used as a part as the first regimen; ** exact Fisher test; *** chisquare test non applicable; *** : others including patients’ decision , adjustement and others reason; **** : biological toxicity includes dyslipidaemia, haematological toxicity and other biological toxicity).
Goto home»