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Clinical studies with anastrozole

  • Chapter
Aromatase Inhibitors

Part of the book series: Milestones in Drug Therapy ((MDT))

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Abstract

Oestrogens play a dominant role in controlling the growth of many breast cancers [1, 2]. The ovaries are the primary source of oestrogen in premenopausal women but ovarian oestrogen production diminishes with age. In postmenopausal women, oestrogens are synthesised by the aromatisation of androgen precursors in the skin, muscle, adipose and breast tissue, including malignant breast tumours [3]. Oestrogen action is inhibited by blocking the oestrogen receptor (ER) with antioestrogens such as tamoxifen, by ovarian ablation using surgery, radiotherapy or luteinising hormone-releasing hormone analogs such as goserelin, or, in postmenopausal women, by blocking oestrogen production by inhibiting aromatase activity [4].

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Howell, A., Wakeling, A. (2008). Clinical studies with anastrozole. In: Furr, B.J.A. (eds) Aromatase Inhibitors. Milestones in Drug Therapy. Birkhäuser Basel. https://doi.org/10.1007/978-3-7643-8693-1_6

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