Evidence map›Paper›PMID 24780050›Full record

ArticleThe Journal of clinical endocrinology and metabolism2014

Abiraterone acetate to lower androgens in women with classic 21-hydroxylase deficiency.

Richard J Auchus, Elizabeth O Buschur, Alice Y Chang, Gary D Hammer, Carole Ramm, David Madrigal, George Wang, Martha Gonzalez, Xu Steven Xu, Johan W Smit and 2 more

2 registry-linked trialsOpen access · bronzeAbstract readClinical Trial, Phase IMulticenter Study
In one paragraph

Article in The Journal of clinical endocrinology and metabolism, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 47 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 1 pooled it
3.4field-weighted citation impact, top 7% of its field
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.

NCT02574910 phase1terminatednot on this mapstarted 2017, after this paper: background citation

A Phase 1 Multi-Center Study to Assess the Efficacy and Safety of Abiraterone Acetate as Adjunctive Therapy in Pre-Pubescent Children With Classic 21-Hydroxylase Deficiency

TypeinterventionalSponsorUniversity of Texas Southwestern Medical CenterRan2017 to 2023Enrolled4ConditionsCongenital Adrenal HyperplasiaArmsAbiraterone acetate
NCT03548246 phase2withdrawnnot on this mapstarted 2023, after this paper: background citation

A Phase 1-2 Multi-Center Study to Assess the Efficacy and Safety of Abiraterone Acetate as Adjunctive Therapy in Pre-Pubescent Children With Classic 21-Hydroxylase Deficiency

TypeinterventionalSponsorUniversity of Texas Southwestern Medical CenterRan2023 to 2026Enrolled0ConditionsCongenital Adrenal HyperplasiaArmsAbiraterone acetate, Placebo, Hydrocortisone, Fludrocortisone
3 · Its place in the literature

Who cites it

47 citing papers in PubMed, 1 synthesis or guideline pooled it, 91 citations in OpenAlex.

  1. Guideline
  2. Trial
  3. Trial
  4. Trial
  5. Trial
  6. Trial
  7. Article
  8. Article
  9. Review
  10. Article
  11. Approach to the Child and Adolescent With Adrenal Insufficiency.The Journal of clinical endocrinology and metabolism · 2025
    Review
  12. Review
  13. Review
  14. Review
  15. Review
  16. Review
  17. Article
  18. Review
  19. Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 4 institutions in 2 countries.

Richard J AuchusDivision of Metabolism, Diabetes, and Endocrinology (R.J.A., E.O.B., G.D.H., C.R., D.M.), University of Michigan, Ann Arbor, Michigan 48109; Division of Endocrinology, Metabolism, Diabetes, and Nutrition (A.Y.C.), Mayo Clinic, Rochester, Minnesota 55905; Janssen Research and Development (G.W., M.G., X.S.X., J.J.), Raritan, New Jersey 08869; Janssen Research and Development (J.W.S.), 2340 Beerse, Belgium; and Janssen Research and Development (M.K.Y.), Los Angeles, California 90024.
Elizabeth O Buschur
Alice Y Chang
Gary D Hammer
Carole Ramm
David Madrigal
George Wang
Martha Gonzalez
Xu Steven Xu
Johan W Smit
James Jiao
Margaret K Yu
Janssen (United States) · USUniversity of Michigan–Ann Arbor · USJanssen (Belgium) · BEMayo Clinic · US

Funding

MICHIGAN INSTITUTE FOR CLINICAL AND HEALTH RESEARCH (MICHR) (UL1): (BPCA)UL1RR024986 · NCRR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SHANLEY, THOMAS P. · 2007 to 2011
$51.2M
Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Mehboob A Hussain · 2013 to 2026
$24.3M
Mechanisms of Adrenal DifferentiationR01DK062027 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GARY D. HAMMER · 2004 to 2026
$8.0M
TRAINING PROGRAM IN ENDOCRINOLOGY AND METABOLISM.T32DK007245 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI RICHARD J. AUCHUS · 1986 to 2026
$7.2M
NCRR NIH HHS UL1 RR024986NCRR NIH HHS UL1-RR024986NIDDK NIH HHS P30 DK020572NIDDK NIH HHS R01 DK062027NIDDK NIH HHS T32 DK007245NIDDK NIH HHS T32DK007245
6 · The paper itself

Abstract

contextChronic supraphysiological glucocorticoid therapy controls the androgen excess of 21-hydroxylase deficiency (21OHD) but contributes to the high prevalence of obesity, glucose intolerance, and reduced bone mass in these patients. Abiraterone acetate (AA) is a prodrug for abiraterone, a potent CYP17A1 inhibitor used to suppress androgens in the treatment of prostate cancer.

objectiveThe objective of the study was to test the hypothesis that AA added to physiological hydrocortisone and 9α-fludrocortisone acetate corrects androgen excess in women with 21OHD without causing hypertension or hypokalemia.

designThis was a phase 1 dose-escalation study.

settingThe study was conducted at university clinical research centers.

participantsWe screened 14 women with classic 21OHD taking hydrocortisone 12.5-20 mg/d to enroll six participants with serum androstenedione greater than 345 ng/dL (>12 nmol/L).

interventionAA was administered for 6 days at 100 or 250 mg every morning with 20 mg/d hydrocortisone and 9α-fludrocortisone acetate.

main outcome measureThe primary endpoint was normalization of mean predose androstenedione on days 6 and 7 (< 230 ng/dL [<8 nmol/L)] in greater than 80% of participants. Secondary end points included serum 17-hydroxyprogesterone and testosterone (T), electrolytes, plasma renin activity, and urine androsterone and etiocholanolone glucuronides.

resultsWith 100 mg/d AA, mean predose androstenedione fell from 764 to 254 ng/dL (26.7-8.9 nmol/L). At 250 mg/d AA, mean androstenedione normalized in five participants (83%) and decreased from 664 to 126 ng/dL (23.2-4.4 nmol/L), meeting the primary end point. Mean androstenedione declined further during day 6 to 66 and 38 ng/dL (2.3 and 1.3 nmol/L) at 100 and 250 mg/d, respectively. Serum T and urinary metabolites declined similarly. Abiraterone exposure was strongly negatively correlated with mean androstenedione. Hypertension and hypokalemia were not observed.

conclusionAA 100-250 mg/d added to replacement hydrocortisone normalized several measures of androgen excess in women with classic 21OHD and elevated serum androstenedione.

Indexed as

17-alpha-HydroxyprogesteroneAbiraterone AcetateAdrenal Hyperplasia, CongenitalAdultAndrogen AntagonistsAndrogensAndrostadienesAndrostenedioneAndrosteroneDesoxycorticosteroneDose-Response Relationship, DrugFemaleHumansHydrocortisoneTreatment Outcome17-alpha-HydroxyprogesteroneAbiraterone AcetateAndrogen AntagonistsAndrogensAndrostadienesAndrostenedioneAndrosteroneandrosterone glucuronideDesoxycorticosteroneHydrocortisone

Identifiers

PMID24780050
PMCPMC4121028
OpenAlexW2079872982

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.