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Review
. 2025 Jul 1;32(7):648-651.
doi: 10.1097/GME.0000000000002537.

The rediscovery of estetrol and its implications for estrogen treatment

Affiliations
Review

The rediscovery of estetrol and its implications for estrogen treatment

Herjan J T Coelingh Bennink et al. Menopause. .

Abstract

Objectives: To summarize the literature on the rediscovery and clinical exploration of the fourth natural estrogen estetrol (E4), more than 100 years after the discovery of estrone (E1), estradiol (E2), and estriol (E3).

Methods: Literature review of E4 publications.

Results: Preclinical and clinical research and development of E4 revealed that: (1) contrary to the other 3 natural estrogens, E4 has a high oral bioavailability, and (2) oral E4 has limited effect on hemostasis and other liver functions, and is, therefore, expected to be a safer estrogen. Since 2022, E4 combined with drospirenone has been registered worldwide as an oral contraceptive. E4 for menopausal hormone therapy is expected to become available in 2026. Clinical development of the use of E4 for the treatment of advanced breast cancer and advanced prostate cancer is ongoing, and E4 has been proposed as a component of an oral male contraceptive.

Conclusion: The recognition of E4 as a useful and safe natural estrogen for human use is expected to change the scene of estrogen treatment in women and men significantly.

Keywords: Estetrol; Natural estrogens; Oral clinical use.

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Conflict of interest statement

Financial disclosure/conflicts of interest: H.J.T.C-B. has retired as President of Pantarhei Bioscience, and is currently president of Pandora Endocrine Innovation BV (PEI), a company involved in the development of new female and male hormonal contraceptives. F.Z.S. has previously received funding from Mithra Pharmaceuticals for manuscript writing. The other authors have nothing to disclose

Figures

FIG. 1
FIG. 1
The 4 estrogens highlighting structure and nomenclature.

References

    1. Allen E, Doisy EA. An ovarian hormone. Preliminary report on its localization, extraction and partial purification, and action in test animals. JAMA 1923;81:819‐821. doi: 10.1001/jama.1923.02650100027012 - DOI - PubMed
    1. Van Iten B, Allen E, Edward A. Doisy’s extraction of estrogen from ovarian follicles, (1923). Embryo Project Encyclopedia 2017. https://hdl.handle.net/10776/11433. Accessed November 18, 2024.
    1. Hagen AA, Barr M, Diczfalusy E. Metabolism of 17-beta-oestradiol-4-14-c in early infancy. Acta Endocrinol (Copenh) 1965;49:207‐220. - PubMed
    1. Gurpide E, Schwers J, Welch MT, Vande Wiele RL, Lieberman S. Fetal and maternal metabolism of estradiol during pregnancy. J Clin Endocrinol Metab 1966;26:1355‐1365. doi:10.1210/jcem-26-12-1355 - PubMed
    1. Holinka CF, Diczfalusy E, Coelingh Bennink HJ. Estetrol: a unique steroid in human pregnancy. J Steroid Biochem Mol Biol 2008;110:138‐143. doi:10.1016/j.jsbmb.2008.03.027 - PubMed

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