Chang Alice Y, Mirfakhraee Sasan, King Elizabeth E, Mercado Jennifer U, Donegan Diane M, Yuen Kevin Cj
Mayo Clinic, Rochester, MN, USA.
UT Southwestern, Dallas, TX, USA.
Clin Med Insights Endocrinol Diabetes. 2021 Mar 4;14:1179551421994102. doi: 10.1177/1179551421994102. eCollection 2021.
Establishing a definitive diagnosis of Cushing disease (CD), given its clinical and biochemical heterogeneity, initiating effective treatment to control the effects of hypercortisolism, and managing recurrence are challenging disease aspects to address. Mifepristone is a competitive glucocorticoid receptor antagonist that is approved in the US by the Food and Drug Administration to control hyperglycemia secondary to endogenous hypercortisolism (Cushing syndrome) in patients who have glucose intolerance or type 2 diabetes mellitus and have failed surgery or are not candidates for surgery. Herein, we describe 6 patients with CD who received mifepristone as adjunct/bridge therapy in the following clinical settings: to assess clinical benefits of treatment for suspected recurrent disease, to control hypercortisolism preoperatively for severe disease, to control hypercortisolism during the COVID-19 pandemic, and to provide adjunctive treatment to radiation therapy. The patients were treated at multiple medical practice settings. Mifepristone treatment in each of the described cases was associated with clinical improvements, including improvements in overall glycemia, hypertension, and weight loss. In addition, in one case where biochemical and radiological evidence of disease recurrence was uncertain, clinical improvement with mifepristone pointed toward likely disease recurrence. Adverse events associated with mifepristone reported in the 6 cases were consistent with those previously reported in the pivotal trial and included cortisol withdrawal symptoms, antiprogesterone effects (vaginal bleeding), hypothyroidism (treated with levothyroxine), and hypokalemia (treated with spironolactone). These cases show how mifepristone can potentially be utilized as a therapeutic trial in equivocal cases of CD recurrence; as a presurgical treatment strategy, particularly during the COVID-19 pandemic; and as bridge therapy, while awaiting the effects of radiation.
鉴于库欣病(CD)在临床和生化方面存在异质性,要做出明确诊断、启动有效治疗以控制高皮质醇血症的影响以及处理复发问题,都是颇具挑战性的疾病相关方面。米非司酮是一种竞争性糖皮质激素受体拮抗剂,在美国已获食品药品监督管理局批准,用于控制葡萄糖不耐受或2型糖尿病且手术失败或不适合手术的患者因内源性高皮质醇血症(库欣综合征)继发的高血糖。在此,我们描述了6例接受米非司酮作为辅助/过渡治疗的CD患者,其临床情况如下:评估疑似复发性疾病治疗的临床获益、术前控制严重疾病的高皮质醇血症、在2019冠状病毒病大流行期间控制高皮质醇血症以及为放射治疗提供辅助治疗。这些患者在多个医疗机构接受治疗。在所描述的每个病例中,米非司酮治疗均与临床改善相关,包括总体血糖、高血压和体重减轻方面的改善。此外,在1例疾病复发的生化和影像学证据不明确的病例中,米非司酮治疗带来的临床改善表明可能存在疾病复发。6例中报告的与米非司酮相关的不良事件与先前在关键试验中报告的一致,包括皮质醇戒断症状、抗孕激素作用(阴道出血)、甲状腺功能减退(用左甲状腺素治疗)和低钾血症(用螺内酯治疗)。这些病例展示了米非司酮如何有可能在CD复发不明确的病例中用作治疗试验;作为术前治疗策略,尤其是在2019冠状病毒病大流行期间;以及作为过渡治疗,同时等待放射治疗的效果。