Medical Therapies: Aromatase Inhibitors

Serdar E. Bulun, Erkut Attar, Bilgin Gürateş, You‐Hong Chen, Hideki Tokunaga, Diana Monsivais, Mary Ellen Pavone
In: Endometriosis · 2011 · pp. 357–365 · doi:10.1002/9781444398519.ch35 · W1546191606
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⚙ AI-generated summary by claude@2026-06, 2026-06-07 ⓘ

Aromatase inhibitors, which block estrogen production, show potential for treating endometriosis by reducing lesion size and pain, and are well-tolerated when combined with other therapies in premenopausal women.

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Abstract

Approximately half of women with endometriosis achieve pain relief from existing medical or surgical treatments. Medical treatments are usually directed at inhibiting estrogen action or its production from the ovaries and do not address local estrogen biosynthesis by the aromatase enzyme in endometriotic lesions. A single gene encodes aromatase, which is the final enzyme in the estrogen biosynthesis pathway, and its inhibition effectively eliminates estrogen production. Recent pilot studies have shown that treatment with an aromatase inhibitor reduced lesion size and pelvic pain. In premenopausal women, an aromatase inhibitor alone may induce ovarian folliculogenesis and thus is combined with a progestin, an oral contraceptive, or a gonadotropin releasing hormone agonist. The side-effect profile of aromatase inhibitors administered in combination with an oral contraceptive or a progestin is remarkably well tolerated. Aromatase inhibitors represent a new class of medications with significant potential for the treatment of endometriosis.

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Condition tags

endometriosis

Citation neighborhood (2-hop)

Papers in the corpus that this work cites (lower rings, blue) and that cite this one (upper rings, green). Dot size scales with the paper's in-corpus citation count — bigger dot = more influential within the endo/adeno field. Click a dot to open that paper. Outer rings show 2-hop neighbours — papers reached through the immediate citers/citees. [ collapse to 1-hop ]

References (88)

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