open access

Vol 73, No 2 (2022)
Review paper
Submitted: 2021-10-12
Accepted: 2021-11-15
Published online: 2022-04-05
Get Citation

Osilodrostat — an emerging drug for the medical management of Cushing’s disease

Przemysław Witek1, Anna Mehlich1, Aleksandra Stasiewicz1, Aleksandra Jawiarczyk-Przybyłowska2, Marek Bolanowski2
·
Pubmed: 35381096
·
Endokrynol Pol 2022;73(2):371-374.
Affiliations
  1. Department of Internal Medicine, Endocrinology, and Diabetes, Medical University of Warsaw, Poland
  2. Chair and Department of Endocrinology, Diabetes, and Isotope Treatment, Wroclaw Medical University, Wroclaw, Poland

open access

Vol 73, No 2 (2022)
Review Article
Submitted: 2021-10-12
Accepted: 2021-11-15
Published online: 2022-04-05

Abstract

Cushing’s disease (CD) is a rare endocrine disorder characterized by the overproduction of adrenocorticotropic hormone (ACTH) by pituitary adenoma followed by hypercortisolaemia with severe complications. Although transsphenoidal resection of the defined pituitary adenoma has been the treatment of choice for the past decades, it does not always result in long-term remission — 10–30% of cases show ineffective surgical treatment or tumour recurrence even after initial success. Pharmacological therapies for cortisol reduction are often required for those who either cannot undergo pituitary surgery or when the surgery has failed, and patients still present with the persistent disease. Osilodrostat is a potent oral steroidogenesis inhibitor that has lately been shown as an effective adjuvant therapy in the management of patients with CD. In this article, we review the recent reports on the efficacy and safety of osilodrostat in clinical settings.

Abstract

Cushing’s disease (CD) is a rare endocrine disorder characterized by the overproduction of adrenocorticotropic hormone (ACTH) by pituitary adenoma followed by hypercortisolaemia with severe complications. Although transsphenoidal resection of the defined pituitary adenoma has been the treatment of choice for the past decades, it does not always result in long-term remission — 10–30% of cases show ineffective surgical treatment or tumour recurrence even after initial success. Pharmacological therapies for cortisol reduction are often required for those who either cannot undergo pituitary surgery or when the surgery has failed, and patients still present with the persistent disease. Osilodrostat is a potent oral steroidogenesis inhibitor that has lately been shown as an effective adjuvant therapy in the management of patients with CD. In this article, we review the recent reports on the efficacy and safety of osilodrostat in clinical settings.

Get Citation

Keywords

Cushing’s disease; hypercortisolism; osilodrostat; steroidogenesis inhibitors; cortisol

About this article
Title

Osilodrostat — an emerging drug for the medical management of Cushing’s disease

Journal

Endokrynologia Polska

Issue

Vol 73, No 2 (2022)

Article type

Review paper

Pages

371-374

Published online

2022-04-05

Page views

5788

Article views/downloads

1026

DOI

10.5603/EP.a2022.0009

Pubmed

35381096

Bibliographic record

Endokrynol Pol 2022;73(2):371-374.

Keywords

Cushing’s disease
hypercortisolism
osilodrostat
steroidogenesis inhibitors
cortisol

Authors

Przemysław Witek
Anna Mehlich
Aleksandra Stasiewicz
Aleksandra Jawiarczyk-Przybyłowska
Marek Bolanowski

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