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Long-term outcomes of osilodrostat in Cushing's disease: LINC 3 study extension

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In this paper , the authors investigated the long-term efficacy and tolerability of osilodrostat, a potent oral 11β-hydroxylase inhibitor, for treating Cushing's disease (CD).
Abstract
Abstract Objective To investigate the long-term efficacy and tolerability of osilodrostat, a potent oral 11β-hydroxylase inhibitor, for treating Cushing's disease (CD). Design/methods A total of 137 adults with CD and mean 24-h urinary free cortisol (mUFC) > 1.5 × upper limit of normal (ULN) received osilodrostat (starting dose 2 mg bid; maximum 30 mg bid) during the prospective, Phase III, 48-week LINC 3 (NCT02180217) core study. Patients benefiting from osilodrostat at week 48 could enter the optional extension (ending when all patients had received ≥ 72 weeks of treatment or discontinued). Efficacy and safety were assessed for all enrolled patients from the core study baseline. Results Median osilodrostat exposure from the core study baseline to study end was 130 weeks (range 1–245) and median average dose was 7.4 mg/day (range 0.8–46.6). The reduction in mean mUFC achieved during the core was maintained during the extension and remained ≤ ULN. Of 106 patients, 86 (81%) patients who entered the extension had mUFC ≤ ULN at week 72. Improvements in cardiovascular/metabolic-related parameters, physical manifestations of hypercortisolism (fat pads, central obesity, rubor, striae, and hirsutism in females), and quality of life in the core study were also maintained or improved further during the extension. No new safety signals were reported; 15/137 (10.9%) and 12/106 (11.3%) patients discontinued for adverse events during the core and extension, respectively. Mean testosterone in females decreased towards baseline levels during the extension. Conclusions Data from this large, multicentre trial show that long-term treatment with osilodrostat sustains cortisol normalisation alongside clinical benefits in most patients with CD and is well tolerated.

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Long-term efficacy and safety of osilodrostat in Cushing’s disease: final results from a Phase II study with an optional extension phase (LINC 2)

TL;DR: In this article , the authors report long-term efficacy and safety data for osilodrostat following completion of an optional extension to LINC 2, where patients with Cushing's disease (CD) were enrolled in a 22-week prospective Phase II study.
Journal ArticleDOI

Glucocorticoid withdrawal syndrome: what to expect and how to manage

TL;DR: In this article , the authors present a review of glucocorticoid withdrawal syndrome (GWS) management after exposure to supraphysiological levels of endogenous or exogenous glucoc corticoids due to an established physical dependence.
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How best to monitor the specific side effects of medical treatments of Cushing's disease.

TL;DR: In this paper , the adverse events associated with these drugs (ketoconazole, levoketoconazoles, metyrapone, osilodrostat, pasireotide, cabergoline and mifepristone) and the way in which to monitor and treat them are discussed.
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Selectivity of osilodrostat as an inhibitor of human steroidogenic cytochromes P450

TL;DR: In this paper , the effect of Osilodrostat (LCI699) on the human steroidogenic cytochromes P450 enzymes (CYP11B1 and CYP11B2) was evaluated using the NCI-H295R human adrenocortical cancer cell line.
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Aldosterone synthase inhibitors and the treatment of essential hypertension.

TL;DR: The Pathway-2 study of treatment-resistant hypertension randomized to receive an additional low dose of spironolactone demonstrated that addition of the mineralocorticoid receptor (MR) antagonist lowered the blood pressure more effectively than placebo, bisoprolol, or doxazosin this paper .
References
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Journal ArticleDOI

Cushing's syndrome

TL;DR: The current understanding of pathogenesis, clinical features, diagnostic, and differential diagnostic approaches, and diagnostic algorithms and recommendations for management of Cushing's syndrome are reviewed.
Journal ArticleDOI

Complications of Cushing's syndrome: state of the art

TL;DR: Cushing's syndrome is a serious endocrine disease caused by chronic, autonomous, and excessive secretion of cortisol, which is associated with increased mortality and impaired quality of life because of the occurrence of comorbidities as discussed by the authors.
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The Treatment of Cushing's Disease

TL;DR: Recent experience suggests that the combination of different drugs may be able to control cortisol excess in a great majority of patients with Cushing's syndrome.
Journal ArticleDOI

Minimal clinically important difference on the Beck Depression Inventory--II according to the patient's perspective.

TL;DR: Improvement in BDI-II scores associated with reporting feeling ‘better’ depended on initial depression severity, and statistical modelling indicated that MCID is best measured on a ratio scale as a percentage reduction of score.
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