Consecutive cyproterone acetate and estradiol treatment in Late-Pubertal transgender female adolescents
Abstract
Background: Cyproterone acetate (CA) is an antiandrogenic progestin commonly used in adult transwomen to suppress endogenous androgens, often in combination with estrogens to induce feminization. Aim: To assess the (side) effects and biochemical changes of CA alone and in combination with estrogens in adolescent trans-girls. Methods: This study was a retrospective analysis of clinical and biochemical data from 27 trans-girls who presented at Tanner stage G4 and were treated with CA monotherapy for at least 6 months (mean = 12 months) and then in combination with incremental doses of estrogens (CA + E; mean = 16 months). Statistical analysis of data included paired or unpaired Student t-test or Wilcoxon signed-ranks or Mann-Whitney U-test as appropriate. Outcomes: Anthropometrics, reported beneficial and side effects, safety parameters, and hormone levels. Results: Physical changes included decrease of facial and non-facial hair growth. One third showed breast development under CA (Tanner stages B2–B3), which increased to Tanner stages B3 and B4 in 66.7% and 9.5% respectively, during CA + E. Reported side effects during CA and CA + E were breast tenderness, emotionality, fatigue, and flushes. No relevant weight changes were observed. Main safety parameters showed the following changes. Hemoglobin and hematocrit decreased and liver enzymes transiently and modestly increased during CA. Triglycerides and cholesterol levels slightly decreased during CA but returned to baseline during CA + E; glucose metabolism was unaffected. Relevant hormonal changes included a decrease in gonadotropins during CA + E and in total and free testosterone levels throughout treatment. Prolactin levels increased during CA and were restored during CA + E. Clinical Implications: CA produced modest feminizing effects in trans-girls and therefore might be a valuable alternative in situations in which gonadotropin-releasing hormone analogues are not the treatment of choice and/or are not reimbursed. Strengths and Limitations: This is the first study to report on the effects of CA in the treatment of trans-girls and one of the few to report on the use of estrogens in this population. Limitations are the modest sample size and the retrospective nature of this study. Conclusion: Treatment with CA in late-pubertal trans-girls overall was safe and well tolerated and induced mild clinical and biochemical feminizing changes. Rapid further feminization was observed with incremental doses of E.
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Although the transwomen in most of the studies achieved testosterone levels within the reference range for cisgender women, there were five studies in which the transfemales had post-GAHT testosterone values greater than 5 nmol/L.
“Although the transwomen in most of the studies achieved testosterone levels within the reference range for cisgender women, there were five studies38 40 47 49 51 in which the transfemales had post-GAHT testosterone values greater than 5 nmol/L.”
Eight of the nine studies found that hormone therapy led to a significant decrease in Hgb/HCT of 4.6%-14.0% (p<0.01).
“Eight of these studies,16 19 36–38 43 48 49 including the large (n=239) ENIGI study,19 found that hormone therapy led to a significant (4.6%–14.0%) decrease in Hgb/HCT (p<0.01)”
Nine studies reported Hgb or HCT levels in transwomen before and after GAHT, with follow-up from a minimum of 3 to a maximum of 36 months post hormone therapy.
“Nine studies16 19 36–38 43 47–49 reported the levels of Hgb or HCT in transwomen before and after GAHT, from a minimum of three to a maximum of 36 months post hormone therapy.”
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References 46 · Cited by 52
- Authors
- Tack, L. J. W., Heyse, R., Craen, M., Dhondt, K., Bossche, H. V., Laridaen, J., & Cools, M.
- Affiliations
- Ghent University Hospital (BE)
- Corresponding author
- Cools, Martine
- Venue
- The Journal of Sexual Medicine
- Publisher
- Oxford University Press (OUP)
- Published
- 2017-05-01
- Volume
- 14
- Issue
- 5
- Pages
- 747-757
- ISSN
- 1743-6095 (ISSN-L)
- 1743-6109
- OpenAlex
- W2612084983
- Semantic Scholar
- 1d3abc37fb542da88d49e2a480217e7f68809a83
- Cited by
- 52
- References
- 46
- Citations by year
- 2026: 3 · 2025: 4 · 2024: 4 · 2023: 4 · 2022: 9 · 2021: 7 · 2020: 5 · 2019: 4 · 2018: 10 · 2017: 2
- FWCI
- 8.22
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- Locations
- The Journal of Sexual Medicine (publishedVersion)
- PubMed (publishedVersion)
- Ghent University Academic Bibliography (Ghent University) (submittedVersion)
- Topics
- Social Sciences › Psychology › Social Psychology › LGBTQ Health, Identity, and Policy
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Sexual Differentiation and Disorders
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Hormonal and reproductive studies
- Keywords
- cyproterone acetate, estradiol, transgender girls, feminizing hormone therapy, breast development, androgen deprivation therapy, gonadotropins, testosterone, prolactin, liver enzymes, hemoglobin, adverse effects, treatment safety, puberty suppression, gender-affirming hormone therapy
- MeSH terms
- Adolescent, Androgen Antagonists, Body Weights and Measures, Drug Therapy, Combination, Estradiol, Estrogens, Female, Humans, Male, Retrospective Studies, Sex Characteristics, Cyproterone Acetate, Transgender Persons
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