Evidence map›Paper›PMID 39288020›Full record

Trial reportThe Journal of clinical endocrinology and metabolism2025

Effect of Spironolactone and Cyproterone Acetate on Breast Growth in Transgender People: A Randomized Clinical Trial.

Lachlan M Angus, Shalem Y Leemaqz, Anna K Kasielska-Trojan, Maksym Mikołajczyk, James C G Doery, Jeffrey D Zajac, Ada S Cheung

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in The Journal of clinical endocrinology and metabolism, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Lachlan M AngusDepartment of Medicine (Austin Health), The University of Melbourne, Melbourne, Victoria 3010, Australia.ORCID 0000-0002-5842-6173
Shalem Y LeemaqzCollege of Medicine and Public Health, Flinders University, South Australia 5042, Australia.ORCID 0000-0003-4616-8426
Anna K Kasielska-TrojanPlastic, Reconstructive, and Aesthetic Surgery Clinic, Medical University of Łódź, 90-419 Łódź, Poland.ORCID 0000-0002-2542-8623
Maksym MikołajczykPlastic, Reconstructive, and Aesthetic Surgery Clinic, Medical University of Łódź, 90-419 Łódź, Poland.ORCID 0000-0001-9828-6526
James C G DoeryDepartment of Pathology, Monash Health, Clayton, Victoria 3168, Australia.ORCID 0000-0002-1235-9913
Jeffrey D ZajacDepartment of Medicine (Austin Health), The University of Melbourne, Melbourne, Victoria 3010, Australia.ORCID 0000-0003-3933-5708
Ada S CheungDepartment of Medicine (Austin Health), The University of Melbourne, Melbourne, Victoria 3010, Australia.ORCID 0000-0001-5257-5525

Funding

Austin Medical Research FoundationNational Health and Medical Research Council #2008956Royal Australasian College of Physicians Foundation
6 · The paper itself

Abstract

contextTransgender people with sex recorded male at birth desiring feminization commonly use cyproterone acetate or spironolactone as antiandrogens with estradiol, but the optimal antiandrogen is unclear.

objectiveWe aimed to assess the effect of antiandrogens on breast development. We hypothesized this would be greater in those treated with cyproterone acetate than spironolactone due to more potent androgen receptor antagonism and suppression of serum total testosterone concentrations.

methodsA randomized clinical trial was conducted between 2020-2022 at an outpatient endocrinology clinic. Transgender people aged 18+ years old commencing feminizing gender affirming hormone therapy were included. The intervention was standardized estradiol therapy plus either spironolactone 100 mg daily or cyproterone acetate 12.5 mg daily for 6 months. The primary outcome was breast development as measured by the breast-chest distance. Secondary outcomes included estimated breast volume, suppression of serum total testosterone concentration <2 nmol/L, and Gender Preoccupation and Stability Questionnaire (GPSQ).

resultsSixty-three people (median age 25 years) were enrolled, randomized, and included in intention to treat analysis (cyproterone acetate n = 32, spironolactone n = 31). At 6 months, there was no between-group difference in breast-chest distance (mean difference 0.27 cm, 95% CI -0.82 to 1.35, P = .6) or estimated breast volume (mean difference 17.26 mL, 95% CI -16.94 to 51.47, P = .3). Cyproterone acetate was more likely to suppress serum testosterone concentration to <2 nmol/L (odds ratio 9.01, 95% CI 1.83 to 4.44, P = .008). Changes in GPSQ were similar between groups.

conclusionAntiandrogen choice should be based on clinician and patient preference with consideration of side effects. Further research is needed to optimize breast development in transgender people.

Indexed as

Androgen AntagonistsBreastCyproterone AcetateSpironolactoneTransgender PersonsAdolescentAdultFemaleHumansMaleTestosteroneYoung AdultAndrogen AntagonistsCyproterone AcetateSpironolactoneTestosteroneantiandrogenfeminizationtestosteronetransgender

Identifiers

PMID39288020
PMCPMC12086416

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.