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. 2023 May 28;41(8):981–997. doi: 10.1007/s40273-023-01277-4

Table 3.

Model input parameters for estimation of costs and effects related to MammaPrint® and endocrine therapy: Probabilities of major adverse events in premenopausal and postmenopausal patients treated with and without ET and probabilities of death from major adverse events

Probabilities of major adverse events—probabilities of thromboembolic events are applied for 5 years and of endometrium cancer and other cancers for 10 years
Post-menopausal women Per cycle (SE—Alpha/Beta) Sources
AI [21] Tamoxifen followed by AI [21] No ET—RR [8]
Thromboembolic events (%) 0.0484 (0.0003–2.4/4850) 0.1038 (0.0005–5/4809) 0.031 (0.001–7/2241/0.00–11/2229a) [8, 21]
Endometrium cancer (%) 0.0057 (0.0004–0.2/3075) 0.0189 (0.0004–0.6/3044) 0.0091 (0.001–8/2240/0.00–5/2235a)
Other cancers (%) 0.1933 (0.0008 –5.9/3069) 0.1732 (0.0008–5.3/3040) 0.1419b (0.002–28/2220/0.003–38/2205a)
Pre-menopausal women Per cycle (SE—Alpha/Beta) Sources
Tamoxifen + ovarian suppression—[9, 43] No ET—[9]
Thromboembolic events (%) 0.063 (0.0005–1/2325) 0.039 (0.0007–0.5/1005) [9, 43]
Endometrium cancer (%) 0.015 (0.0004–1.7/3577) 0.010 (0.0004–1.7/3573)
Other cancers (%) 0.122 (0.0004–1.7/3577) 0.109 (0.0004–1.7/3573)
Death from: Per cycle (SE) Sources
Thromboembolic events (%) 7.7 (0.006–91/1111b) [9, 22]
Endometrium cancer (%) 21 (0.021–78/296b) [44]
Other cancers (%) 27 (0.027–72/197b) Assumptions

Values in italics indicate SE—Alpha/Beta

AI aromatase inhibitor, ET endocrine therapy, RR relative risk, SE standard error

aProbabilistic RRs were calculated by dividing two probabilities and using the SE of both. Probabilistic RRs were applied to the probabilistic

bSE assumed to be 10% of mean values of exemestane