Table 1.
Menopausal status at time of diagnosis | Type of endocrine therapy | Reasons for therapy selection | Extended therapy: considerations | Type of extended therapy |
---|---|---|---|---|
Postmenopausal | AI (5 years) | High risk of early relapse History of thromboembolic disease Depression |
No significant OS benefit Shared decision making if N2, N3, and AI well tolerated | AI (2 years) |
AI (2–3 years) -> Tam (2–3 years) |
Higher risk Relevant cardiovascular disease |
High risk, e.g., N2, N3, and treatment well tolerated | AI (2–5 years) or Tam (2–5 years) | |
Tam (2–3 years) -> AI (2–3 years) |
Intermediate risk Osteopenia/osteoporosis Relevant cardiovascular disease | High risk, e.g., N2, N3, and treatment well tolerated | AI (2–5 years) or Tam (2–5 years) | |
Tam (5 years) | Low risk | Higher risk | AI (2–5 years) or Tam (5 years) | |
Peri- and Premenopausal | Tam (5 years) | Low and intermediate risk | Intermediate risk | Tam (5 years) or AI (2–5 years) if postmenopausala |
Tam (5 years) + OFS (2–5 years) | <35 years or becoming premenopausal during the 2 years following chemotherapy | High risk | Tam (5 years) or AI (5 years) if postmenopausala | |
OFS (up to 5 years) | Tam contraindicated and low risk | - | - | |
AI + OFS (5 years) | Tam contraindicated and intermediate or high risk | - | - |
AI, aromatase inhibitor; Tam, tamoxifen; OFS, ovarian function suppression; COF, chemotherapy-induced ovarian failure.
Testing of E2/FSH after COF repeatedly before and during treatment. Treat osteopenia and osteoporosis according to guidelines; consider bisphosphonate oral or intravenous in osteoprotective dosage for patients (1) more than 5 years after menopause or (2) during therapy with AI or OFS.