Abstract

Cushing's disease (CD) is a serious endocrine disorder characterized by chronic hypercortisolism, or Cushing's syndrome (CS), caused by a corticotroph pituitary tumor, which induces an excessive adrenocorticotropic hormone (ACTH) and consequently cortisol secretion. CD presents a severe clinical burden, with impairment of the quality of life and increase in mortality. Pituitary surgery represents the first-line therapy, but it is non-curative in one third of patients, requiring additional treatments. Among second-line treatments, medical therapy is gradually gaining importance, although the current medical treatments are unable to reach optimal efficacy and safety profile. Therefore, new drugs and new formulations of presently available drugs are currently under clinical investigation in international clinical trials, in order to assess their efficacy and safety in CD, or in the general population of CS. Among pituitary-directed agents, pasireotide, in the twice-daily subcutaneous formulation, has been demonstrated to be an effective treatment both in clinical trials and in real-world studies, and extension studies of the phase II and III clinical trials reported evidence of long-term efficacy with general good safety profile, although associated with frequent hyperglycemia, which requires monitoring of glucose metabolism. Moreover, the most recent once-monthly intramuscular formulation, pasireotide long-acting release (LAR), showed similar efficacy and safety, but associated with potential better compliance profile in CD. Roscovitine is an experimental drug currently under investigation. Among adrenal-directed agents, metyrapone is the only historical agent currently under investigation in a prospective, multicenter, international clinical trial, that would likely clarify its efficacy and safety in a large population of patients with CS. Osilodrostat, a novel agent with a mechanism of action similar to metyrapone, seems to offer a rapid, sustained, and effective disease control of CD, according to recently completed clinical trials, whereas levoketoconazole, a different chemical formulation of the historical agent ketoconazole, is still under investigation in clinical trials, with preliminary evidences showing an effective and safe control of CS. ATR-101 is an experimental drug currently under investigation. Among glucocorticoid receptor-directed drugs, mifepristone has been demonstrated to improve clinical syndrome and comorbidities, especially hypertension and impairment of glucose metabolism, but the occurrence of hypokalemia and in women uterine disorders, due to the concomitant action on progestin receptor, requires caution, whereas the preliminary evidence on relacorilant, characterized by high selectivity for glucocorticoid receptor, suggested good efficacy in the control of hypertension and impairment of glucose metabolism, as well as a good safety profile, in CS. Finally, a limited experience has demonstrated that combination therapy might be an interesting approach in the management of CD. The current review provides a summary of the available evidences from current and recent clinical trials on CD, with a specific focus on preliminary data.

Highlights

  • Cushing’s disease (CD) is a rare and serious endocrine disorder characterized by excessive adrenocorticotropic hormone (ACTH) secretion by a corticotroph pituitary tumor, driving an excessive cortisol secretion by the adrenal glands

  • The current review aims to summarize the presently available evidences from currently on-going and recently completed clinical trials on CD, offering a summary of either definitive reports published in scientific literature or preliminary data presented at scientific meetings

  • Experimental studies on murine corticotroph pituitary tumor cell lines and human corticotroph pituitary tumor cell cultures demonstrated that pasireotide induced a significant decrease in ACTH secretion (4, 7); interestingly, the inhibition of ACTH secretion was maintained even in cultures pre-incubated with dexamethasone, supporting the hypothesis of a predominant role of SSTR5 in the regulation of corticotroph cell secretion during chronic hypercortisolism (7, 10)

Read more

Summary

INTRODUCTION

Cushing’s disease (CD) is a rare and serious endocrine disorder characterized by excessive adrenocorticotropic hormone (ACTH) secretion by a corticotroph pituitary tumor, driving an excessive cortisol secretion by the adrenal glands. Three main drug categories may be identified: pituitary-directed drugs, including pasireotide and cabergoline; adrenal-directed drugs, or steroidogenesis inhibitors, including ketoconazole, metyrapone, and mitotane; and glucocorticoid receptor (GR)-directed drugs, or GR antagonists, mainly represented by mifepristone (3, 4) None of these compounds is currently able to completely reach the therapeutic goals of treatment for CD (4). On the basis of this evidence, in the early 2000s, preclinical and clinical investigations were started on a multi-ligand SSA, pasireotide, with relevant affinity for SSTR type 1 (SSTR1), SSTR2, SSTR type 3 (SSTR3), and TABLE 1 | Summary of the available data regarding drugs evaluated in recent clinical trials or under investigation, registered in clinicaltrials.gov, in Cushing’s disease and Cushing’s syndrome in terms of administration route and timing, available dosages, remission rate, and safety profile

Twice daily
Pasireotide LAR Roscovitine
Metyrapone Osilodrostat
Mifepristone Relacorilant
COMBINATION THERAPY
CONCLUSIONS
Findings
AUTHOR CONTRIBUTIONS
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call