Table 1.
Utilities | Weighted average values | Original values (distributions) | Source |
---|---|---|---|
Base state–Stable disease | 0.715 | 0.715 | Lloyd et al. [9] |
Disutility | |||
Grade 3 and 4 adverse events | |||
Arm 1 | |||
Stomatitis | 0.01208 | 0.151 (8 %) | Lloyd et al. [9]; Baselga et al. [3] |
Anemia | 0.00906 | 0.151 (6 %)a | Lloyd et al. [9]; Baselga et al. [3] |
Dyspnea | 0.00604 | 0.151 (4 %)a | Lloyd et al. [9]; Baselga et al. [3] |
Hyperglycemia | 0.00604 | 0.151 (4 %)a | Lloyd et al. [9]; Baselga et al. [3] |
Fatigue | 0.0046 | 0.115 (4 %) | Lloyd et al. [9]; Baselga et al. [3] |
Pneumonitis | 0.00453 | 0.151 (3 %)a | Lloyd et al. [9]; Baselga et al. [3] |
Arm 0 | |||
Stomatitis | 0.00151 | 0.151 (1 %) | Lloyd et al. [9]; Baselga et al. [3] |
Anemia | 0.00151 | 0.151 (1 %)a | Lloyd et al. [9]; Baselga et al. [3] |
Dyspnea | 0.00151 | 0.151 (1 %)a | Lloyd et al. [9]; Baselga et al. [3] |
Hyperglycemia | 0.00151 | 0.151 (1 %)a | Lloyd et al. [9]; Baselga et al. [3] |
Fatigue | 0.00115 | 0.115 (1 %) | Lloyd et al. [9]; Baselga et al. [3] |
Pneumonitis | 0 | 0.151 (0 %)a | Lloyd et al. [9]; Baselga et al. [3] |
Treatment arm 0: Exemestane only; Treatment arm 1: Everolimus plus Exemestane
To obtain the utility decrements for adverse events, for which values were not available in the literature, we multiplied the highest utility decrement value available (0.151) by the proportion of patients experiencing these adverse events