Skip to main content
. Author manuscript; available in PMC: 2015 Dec 1.
Published in final edited form as: Dig Dis Sci. 2014 Aug 8;59(12):3043–3052. doi: 10.1007/s10620-014-3294-0

Table 1.

Baseline characteristics of treated cohort, by treatment group

Total (N=352) Telaprevir (n=211) Boceprevir (n=141)
Age, median (range) 56 (21, 70) 57 (25, 70) 56 (21, 69)
Male 213 (61%) 125 (59%) 88 (62%)
Race/ethnicity
  Black 52 (15%) 34 (16%) 18 (13%)
  Asian 18 (5%) 8 (4%) 10 (7%)
  Hispanic 52 (15%) 31 (15%) 21 (15%)
  White non-Hispanic 223 (63%) 135 (64%) 88 (62%)
  Unknown/other 7 (2%) 3 (1%) 4 (3%)
Health plan membership
  <12 months 14 (4%) 8 (4%) 6 (4%)
  12–59 months 122 (35%) 74 (35%) 48 (34%)
  ≥60 months 216 (61%) 129 (61%) 87 (62%)
Diabetes 58 (16%) 34 (16%) 24 (17%)
Body mass index
  <25 kg/m2 87 (25%) 52 (25%) 35 (25%)
  25–30 kg/m2 138 (39%) 83 (39%) 55 (39%)
  ≥30 kg/m2 127 (36%) 76 (36%) 51 (36%)
HCV treatment history
  Naïve 198 (56%) 113 (54%) 85 (60%)
  Relapse/breakthrough 41 (12%) 27 (13%) 14 (10%)
  Partial responder 25 (7%) 18 (9%) 7 (5%)
  Null responder 38 (11%) 27 (13%) 11 (8%)
  Treatment experienced, response unknown 50 (14%) 26 (12%) 24 (17%)
Fibrosis stage+
  F0 7 (6%) 6 (8%) 1 (2%)
  F1–F2 60 (48%) 29 (38%) 31 (62%)
  F3 45 (36%) 30 (39%) 15 (30%)
  F4 14 (11%) 11 (14%) 3 (6%)
Cirrhosis* 73 (21%) 48 (23%) 25 (18%)
HCV subtype
  1a 218 (62%) 132 (63%) 86 (61%)
  1b 111 (32%) 67 (32%) 44 (31%)
  1 other/unknown 23 (7%) 12 (6%) 11 (8%)
HCV viral load
  <400,000 IU/mL 92 (26%) 57 (27%) 35 (25%)
  400,000–799,999 IU/mL 60 (17%) 36 (17%) 24 (17%)
  ≥800,000 IU/mL 189 (54%) 114 (54%) 75 (53%)
  Missing 11 (3%) 4 (2%) 7 (5%)
Platelet count (×109/L)
  <150 110 (31%) 68 (32%) 42 (30%)
  ≥150 229 (65%) 139 (66%) 90 (64%)
  Missing 13 (4%) 4 (2%) 9 (6%)

HCV= hepatitis C virus;

+

Fibrosis measured using the Batts-Ludwig scale among subjects with liver biopsy performed (total=126, telaprevir=76, boceprevir=50);

*

Cirrhosis by clinical diagnosis or liver biopsy