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Table 2 Treatment characteristics from SPRINT-2 [17]

From: Boceprevir for previously untreated patients with chronic hepatitis C Genotype 1 infection: a US-based cost-effectiveness modeling study

A. Efficacy and Discontinuation Rates

 

Non-Black Cohort

Black Cohort

 

PR48

BOC/RGT

BOC/PR48

PR48

BOC/RGT

BOC/PR48

 

(N = 311)

(N = 316)

(N = 311)

(N = 52)

(N = 52)

(N = 55)

Sustained virologic response,% (95% confidence interval) distribution

40.2 (34.7–45.9)

66.8 (61.3–71.9)

68.5 (63.0–73.6)

23.1 (12.5–45.9)

42.3 (28.7–56.8)

52.7 (38.8–66.3)

Beta (123.00, 183.02)

Beta (212.7, 105.85)

Beta (216.12, 99.43)

Beta (123.00, 183.02)

Beta (212.7, 105.85)

Beta (216.12, 99.43)

Probability of discontinuation before Week 24 for reasons other than futility, n/m (%)

46/311 (14.8)

49/316 (15.5)

46/311 (14.8)

10/52 (19.2)

12/52 (23.5)

8/55 (14.5)

Probability of discontinuation after Week 24 for reasons other than futility, n/m (%)

25/173 (14.5)

20/225 (8.9)

42/232 (18.1)

6/17 (33.3)

3/27 (11.1)

8/33 (22.9)

Probability of failing futility rule at Week 24, n/m (%)

92/265 (34.7)

42/267 (15.7)

33/265 (12.5)

25/42 (59.5)

13/40 (32.5)

14/47 (29.8)

Probability of being assigned and completing 28 weeks of treatment, n (%)

NA

147 (46.5)

NA

NA

15 (28.8)

NA

B. Side Effects

Combined Cohorts

 

PR48

BOC/RGT

BOC/PR48

 

(N = 363)

(N = 368)

(N = 366)

Anemia, n (%)

107 (29.5)

182 (49.5)

180 (49.2)

Erythropoietin use, n (%)

87 (24.0)

159 (43.2)

159 (43.4)

Mean duration of anemia, Days

128.3

107.9

145.0

Mean duration of erythropoietin use, days

121.4

93.5

156.4

  1. PR48 – peginterferon-ribavirin regimen for 48 weeks; BOC/RGT – peginterferon-ribavirin and boceprevir for 24 weeks, and those with a detectable hepatitis C virus (HCV) RNA level between weeks 8 and 24 received peginterferon–ribavirin from week 28 to week 48; BOC/PR48 –peginterferon–ribavirin for 48 weeks and boceprevir for 44 weeks.