Table 2.
Health state | Base case: Woehl et al. (2008) [28] |
Vedolizumab IV trial data (GEMINI 1) [8] |
---|---|---|
Clinical remission | 0.87 | 0.86 |
Clinical response | 0.76 | 0.80 |
Active UC | 0.41 | 0.67 |
Surgery | 0.66a | 0.67 |
Post-surgery remission | 0.71 | 0.68 |
Post-surgery complications | 0.66a | 0.49 |
AEs | Utility decrements associated with AEs | |
---|---|---|
Disutility | Duration, weeks | |
Serious infection | − 0.520 | 10 |
Upper respiratory tract infection | − 0.550 | 10 |
Tuberculosis | − 0.550 | 10 |
Malignancies | − 0.195 | 10 |
Acute infusion-related AE | − 0.110 | 10 |
Injection-site reaction | − 0.030 | 10 |
Herpes zoster | − 0.190 | 10 |
Myocardial infarction | − 0.125 | 10 |
Stroke | − 0.139 | 10 |
AE adverse event, IV intravenous, SC subcutaneous, UC ulcerative colitis
aCalculated as the weighted average of the utility score for surgery used in the cost-effectiveness analysis of infliximab IV, adalimumab SC, and golimumab SC by the National Institute of Health and Care Excellence Assessment Group (0.41) during 8 weeks and the utility score for post-surgery remission (0.71), taken as the average from Archer et al. (2016) [14] and Woehl et al. (2008) [28] for the remainder of the year (i.e., 44 weeks): 0.66 = 0.41 × (8 ⁄ 52) + 0.71 × (44 ⁄ 52)