Dipartimento di Medicina Clinica e Chirurgia, Sezione di Endocrinologia, Università Federico II di Napoli, Naples, Italy.
UNESCO Chair for Health Education and Sustainable Development, Federico II University, Naples, Italy.
Front Endocrinol (Lausanne). 2020 Dec 8;11:648. doi: 10.3389/fendo.2020.00648. eCollection 2020.
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.
库欣病(CD)是一种严重的内分泌疾病,其特征为慢性皮质醇增多症,即库欣综合征(CS),由促肾上腺皮质激素垂体肿瘤引起,导致促肾上腺皮质激素(ACTH)过度分泌,进而导致皮质醇分泌增加。CD 会给患者带来严重的临床负担,影响生活质量并增加死亡率。垂体手术是一线治疗方法,但三分之一的患者无法治愈,需要额外的治疗。在二线治疗中,药物治疗逐渐受到重视,尽管目前的药物治疗无法达到最佳的疗效和安全性。因此,新的药物和现有药物的新制剂正在国际临床试验中进行临床研究,以评估它们在 CD 或 CS 一般人群中的疗效和安全性。在针对垂体的药物中,帕瑞肽(每天两次皮下注射)已在临床试验和真实世界研究中被证明是一种有效的治疗方法,而 II 期和 III 期临床试验的扩展研究报告了长期疗效的证据,且安全性良好,尽管与频繁的高血糖有关,需要监测血糖代谢。此外,最近的每月一次肌内注射制剂帕瑞肽长效释放(LAR)显示出相似的疗效和安全性,但在 CD 中可能具有更好的依从性。罗西维林是一种正在研究的实验药物。在针对肾上腺的药物中,美替拉酮是目前唯一正在前瞻性、多中心国际临床试验中研究的历史药物,这可能会在 CS 的大患者人群中明确其疗效和安全性。奥西罗酮是一种作用机制类似于美替拉酮的新型药物,根据最近完成的临床试验,它似乎可以快速、持续和有效地控制 CD,而不同化学配方的历史药物酮康唑的左旋酮康唑仍在临床试验中,初步证据表明其可以有效安全地控制 CS。ATR-101 是一种正在研究的实验药物。在糖皮质激素受体靶向药物中,米非司酮已被证明可以改善临床综合征和合并症,特别是高血压和葡萄糖代谢受损,但由于对孕激素受体的共同作用,会导致低钾血症和女性子宫疾病,需要谨慎,而初步证据表明,高选择性糖皮质激素受体的雷卡洛尔在控制高血压和葡萄糖代谢受损方面具有良好的疗效和安全性,以及良好的安全性,在 CS 中。最后,有限的经验表明,联合治疗可能是 CD 管理的一种有趣方法。本综述提供了当前和最近 CD 临床试验的现有证据总结,特别关注初步数据。