A djuvant endocrine therapy improves oncological outcomes in women with oestrogen receptor-positive early breast cancer, but can accelerate bone loss, which predisposes to increased fracture risk. We summarise recommendations on the assessment and management of bone health in such women. The full position statement is available at https ://onlin elibr ary.wiley. com/doi/epdf/10. 1111/cen.13735 . 1 In Australia, dual energy x-ray absorptiometry imaging is not currently subsidised for women receiving adjuvant endocrine therapies for oestrogen receptor-positive breast cancer, and the use of anti-resorptive treatment in this population is generally off label.Adjuvant endocrine therapies for oestrogen receptor-positive breast cancer include aromatase inhibitors (anastrozole, exemestane, letrozole) or selective oestrogen receptor modulators, usually tamoxifen. Aromatase inhibitors block oestradiol production, resulting in > 98% deprivation of circulating oestradiol in post-menopausal women. Aromatase inhibitors inhibit the oestradiol-mediated negative feedback on gonadotropin production and cannot be used as breast cancer treatment in premenopausal women unless ovarian function is suppressed (eg, by gonadotropin-releasing hormone agonists or bilateral oophorectomy). Selective oestrogen receptor modulators act as oestrogen receptor antagonists in the breast but have partial agonistic activity in tissues such as bone and endometrium, and may be used in both pre-and post-menopausal women.In post-menopausal women, aromatase inhibitors are preferred because of modest improvements in outcomes, including lower 10-year breast cancer mortality compared with tamoxifen (12.1% v 14.2%; relative risk, 0.85; 95% CI, 0.75-0.96; P < 0.01). 2 Increasing the duration of endocrine therapy from 5 to 10 years can reduce the risk of breast cancer recurrence, 3,4 but the absolute benefit is modest, and no survival benefit has been reported to date. In premenopausal women, tamoxifen has traditionally been first line treatment, although, on the background of ovarian suppression, the aromatase inhibitor exemestane improved 5-year diseasefree survival compared with tamoxifen (91.1% v 87.3%; hazard ratio, 0.72; 95% CI, 0.60-0.85; P < 0.001). 5 These benefits have been confirmed by a recent 8-year follow-up study. 6 In women < 35 years of age, the 5-year breast cancer-free interval was 67.1% (95% CI, 54.6-76.9%) with tamoxifen alone, 75.9% with tamoxifen plus ovarian suppression (95% CI, 64.0-84.4%), and 83.2% with exemestane plus ovarian suppression (95% CI, 72.7-90.0%). 7 After 8 years, the rate of freedom from distant recurrence in this age group was 73.8% with tamoxifen alone, 77.5% with tamoxifen plus ovarian suppression, and 82.4% with exemestane plus ovarian suppression. 6 These data 5-7 are expected to increase the number of young, pre-menopausal women receiving ovarian suppression combined with aromatase inhibitors, which has profound effects on bone health (Box 1).Due to earlier detection and advances in adjuvant treatment, women wit...