Cited by 201Pituitary Gland Disorders and TreatmentsAdrenal and Paraganglionic TumorsAdrenal Hormones and Disorders

Ketoconazole treatment in Cushing’s syndrome: experience in 34 patients

Sonino, Nicoletta, Boscaro, Marco, Paoletta, Agostino, Mantero, Franco, Zillotto, Donato·1991·Clinical Endocrinology

Abstract

OBJECTIVE: Ketoconazole treatment of Cushing's syndrome has been reported in single cases and a few small groups of 5-8 patients. We report our experience in 34 patients. DESIGN: Clinical study, with pretreatment and post-treatment evaluations. PATIENTS: Out of 67 patients with Cushing's syndrome admitted during the last 6 years, 34 (28 females/six males; age range 14-67 years) received ketoconazole as a palliative treatment due to severe clinical conditions or management of the disease while awaiting results of definitive therapy. MEASUREMENTS: Urinary cortisol, plasma cortisol and ACTH, and routine chemistry were measured every week for 4 weeks, and then once a month. RESULTS: Comparing the last values (mean +/- SEM) during treatment with baseline, urinary cortisol decreased from 1296 +/- 176 to 270 +/- 69 nmol/d (n = 34; P less than 0.001); plasma cortisol decreased from 672 +/- 31 to 549 +/- 35 nmol/l (n = 34; P less than 0.001). For patients with pituitary-dependent Cushing's syndrome, urinary cortisol decreased from 1073 +/- 126 to 200 +/- 21 nmol/d (n = 28; P less than 0.001) while plasma ACTH changed from 12.5 +/- 1.3 to 11.3 +/- 0.8 pmol/l (n = 26; not significant). Twelve patients were treated for more than 6 months, and those with pituitary-dependent disease all received pituitary radiation therapy, except the two who eventually escaped pharmacological control. One additional patient with adrenal carcinoma and one with ectopic ACTH syndrome showed lack of control of urinary cortisol levels. Ketoconazole was withdrawn within the first week in two patients for allergic reaction and acute liver toxicity. Other side-effects included: asymptomatic liver function abnormalities in three patients; gastrointestinal symptoms in four; worsening of gynaecomastia in one. Rapid clinical improvement was observed together with the normalization of urinary cortisol levels, with regression of symptoms such as diabetes mellitus, hypertension, hypokalaemia, and restoration of well being. CONCLUSIONS: These data confirm that ketoconazole is valuable in the management of hypercortisolism, provided that patients are closely watched to exclude those who may develop liver toxicity and to prevent the occurrence of adrenal insufficiency.

Integrity signals

Registry

Crossref · 10.1111/j.1365-2265.1991.tb03547.x

Cites

20 of 20 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • At doses of 200 to 1200 mg daily, ketoconazole has been shown to improve glucose metabolism in patients with Cushing syndrome and in those with type 2 diabetes.

    “At doses of  to  mg daily, this steroidogenesis inhibitor has been shown to improve glucose metabolism in patients with CS and in those with type  DM (-).”

Cites

Flagged first, then by citations

Cited by

Sorted by citations

Authors
Sonino, N., Boscaro, M., Paoletta, A., Mantero, F., & Zillotto, D.
Affiliations
  • University of Padua (IT)
  • University of Catania (IT)
Corresponding author
Sonino, Nicoletta
Venue
Clinical Endocrinology
Publisher
Wiley
Published
1991-10
Volume
35
Issue
4
Pages
347-352
ISSN
  • 0300-0664 (ISSN-L)
  • 1365-2265
OpenAlex
W1966571242
Cited by
201
References
20
Citations by year
2026: 2 · 2025: 3 · 2024: 6 · 2023: 4 · 2022: 5 · 2021: 7 · 2020: 5 · 2019: 9 · 2018: 7 · 2017: 5 · 2016: 5 · 2015: 10 · 2014: 10 · 2013: 9 · 2012: 12
FWCI
3.88
Type
journal article
Language
en
Open access
closed
Locations
  • Clinical Endocrinology (publishedVersion)
  • PubMed (publishedVersion)
  • Padua Research Archive (University of Padova) (submittedVersion)
Topics
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Pituitary Gland Disorders and Treatments
  • Health Sciences › Medicine › Surgery › Adrenal and Paraganglionic Tumors
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adrenal Hormones and Disorders
Keywords
ketoconazole, Cushing's syndrome, hypercortisolism, pituitary-dependent Cushing's disease, adrenocortical carcinoma, ectopic ACTH syndrome, urinary cortisol, plasma cortisol, ACTH, hepatotoxicity, adverse drug reactions, palliative care, diabetes mellitus, hypertension, hypokalemia, gynecomastia
MeSH terms
Adolescent, Adult, Aged, Cushing Syndrome, Drug Administration Schedule, Female, Humans, Hydrocortisone, Ketoconazole, Male, Middle Aged, Chemical and Drug Induced Liver Injury

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review