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Original Research

Use of bone-modifying agents among breast cancer patients with bone metastasis: evidence from oncology practices in the US

, , , , , , & show all
Pages 1349-1358 | Published online: 26 Sep 2018

Figures & data

Table 1 Baseline characteristicsTable Footnotea of women with bone metastasis from breast cancer eligible for initiating, interrupting, or reinitiating BMAs

Figure 1 Cumulative incidence of bone-modifying agent initiation (A), interruption, and reinitiation (B) among patients with bone metastasis from breast cancer in the US, 2013–2016.

Abbreviation: BMA, bone-modifying agent.
Figure 1 Cumulative incidence of bone-modifying agent initiation (A), interruption, and reinitiation (B) among patients with bone metastasis from breast cancer in the US, 2013–2016.

Figure 2 Adjusted risk difference estimates per 100 for variables associated with bone-modifying agent initiation (A) and interruption (B).

Note: Each estimate in the model was adjusted for all other variables listed as well as alkaline phosphatase level and serum calcium level.
Abbreviations: ECOG, Eastern Cooperative Oncology Group Performance Status; eGFR, estimated glomerular filtration rate; ER, estrogen receptor; HER2, human epidermal growth factor receptor 2; PR, progesterone receptor; SRE, skeletal-related event.
Figure 2 Adjusted risk difference estimates per 100 for variables associated with bone-modifying agent initiation (A) and interruption (B).