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10.1186/s40842-016-0033-9

http://scihub22266oqcxt.onion/10.1186/s40842-016-0033-9
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C5471955!5471955!28702250
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suck abstract from ncbi

pmid28702250      Clin+Diabetes+Endocrinol 2016 ; 2 (ä): ä
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  • Update on medical treatment for Cushing?s disease #MMPMID28702250
  • Cuevas-Ramos D; Lim DST; Fleseriu M
  • Clin Diabetes Endocrinol 2016[]; 2 (ä): ä PMID28702250show ga
  • Cushing?s disease (CD) is the most common cause of endogenous Cushing?s syndrome (CS). The goal of treatment is to rapidly control cortisol excess and achieve long-term remission, to reverse the clinical features and reduce long-term complications associated with increased mortality.While pituitary surgery remains first line therapy, pituitary radiotherapy and bilateral adrenalectomy have traditionally been seen as second-line therapies for persistent hypercortisolism. Medical therapy is now recognized to play a key role in the control of cortisol excess. In this review, all currently available medical therapies are summarized, and novel medical therapies in phase 3 clinical trials, such as osilodrostat and levoketoconazole are discussed, with an emphasis on indications, efficacy and safety. Emerging data suggests increased efficacy and better tolerability with these novel therapies and combination treatment strategies, and potentially increases the therapeutic options for treatment of CD. New insights into the pathophysiology of CD are highlighted, along with potential therapeutic applications. Future treatments on the horizon such as R-roscovitine, retinoic acid, epidermal growth factor receptor inhibitors and somatostatin-dopamine chimeric compounds are also described, with a focus on potential clinical utility.
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