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. Author manuscript; available in PMC: 2019 Apr 1.
Published in final edited form as: Med Decis Making. 2018 Apr;38(1 Suppl):140S–150S. doi: 10.1177/0272989X17718168

Table 2.

Model inputs used for the Age trial simulation:

Model Input Description Source
Population demographics
  Birth cohort Birth years of women participating in the Age trial Age trial
  Life years Number of life years by trial arm by age Age trial
Natural history of breast cancer
  Incidence Control arm incidence (incidence in the absence of screening) Age trial
  Tumor onset The moment tumors start to grow (tumor inception) CISNET1
  Sojourn time Time between when a cancer is first screen-detectable and cancer diagnosis in the absence of screening. CISNET2
  Tumor progression Tumor growth, tumor progression and regression affect tumor sojourn times and breast cancer survival. CISNET3
  Estrogen receptor distribution Age-specific ER positive and ER negative distributions U.K.4
Breast cancer screening
  Attendance Adherence to annual screening in the intervention arm Age trial
  Sensitivity Probability that the screen will be positive among women with breast cancer by age, screening round (first vs. subsequent) Age trial
  Mammography Two-view mammography for first screens, for all subsequent screens one-view mammography Age trial
Breast cancer treatment
  Treatment dissemination Breast cancer treatment by age, stage and ER-status BASO5
  Effectiveness Hazard reduction breast cancer mortality by age and ER-status EBCTCG6
Breast cancer survival
  Survival Breast cancer survival by age, stage and ER-status CISNET7
  Other-cause mortality Probability of dying from causes other than breast cancer U.K.8
1–3

Tumor onset, sojourn time and tumor progression are model-specific parameters. These, and other model-specific assumptions about breast cancer natural history are described elsewhere [6, 2125].

4

Estrogen receptor status comes from observed U.K. data [26].

5

The treatment dissemination was derived from BASO reports [26] published by the NHSBSP.

6

Treatment effectiveness / hazard reduction for breast cancer death was published by the Early Breast Cancer Trialists Collaborative Group (EBCTCG) that included the U.K. trials [27]

7

Breast cancer survival by age and ER status from the UK is not available for the time period of the trial, the existing survival in the models which is based on U.S. data was used.

8

Other cause mortality was taken from the Human Mortality Database [30] with breast cancer deaths removed.