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

J Clin Endocrinol Metab. 2014 Aug;99(8):2763-70. doi: 10.1210/jc.2014-1258. Epub 2014 Apr 29.

Abstract

Context: Chronic 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.

Objective: The 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.

Design: This was a phase 1 dose-escalation study.

Setting: The study was conducted at university clinical research centers.

Participants: We 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).

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

Main outcome measure: The 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.

Results: With 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.

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

Publication types

  • Clinical Trial, Phase I
  • Multicenter Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • 17-alpha-Hydroxyprogesterone / blood
  • Abiraterone Acetate
  • Adrenal Hyperplasia, Congenital / blood*
  • Adrenal Hyperplasia, Congenital / drug therapy*
  • Adult
  • Androgen Antagonists / administration & dosage*
  • Androgen Antagonists / adverse effects
  • Androgen Antagonists / pharmacokinetics
  • Androgens / blood*
  • Androstadienes / administration & dosage*
  • Androstadienes / adverse effects
  • Androstadienes / pharmacokinetics
  • Androstenedione / blood
  • Androstenedione / urine
  • Androsterone / analogs & derivatives
  • Androsterone / urine
  • Desoxycorticosterone / blood
  • Dose-Response Relationship, Drug
  • Female
  • Humans
  • Hydrocortisone / administration & dosage
  • Treatment Outcome

Substances

  • Androgen Antagonists
  • Androgens
  • Androstadienes
  • androsterone glucuronide
  • Androstenedione
  • Desoxycorticosterone
  • 17-alpha-Hydroxyprogesterone
  • Androsterone
  • Abiraterone Acetate
  • Hydrocortisone

Supplementary concepts

  • Congenital adrenal hyperplasia due to 21 hydroxylase deficiency