University of Arizona, Phoenix, AZ, USA.
Phoenix VA Medical Center, Phoenix, AZ, USA.
J Investig Med High Impact Case Rep. 2020 Jan-Dec;8:2324709620936808. doi: 10.1177/2324709620936808.
Tyrosine kinase inhibitors (TKIs) have been used in the treatment of multiple types of cancer. Pazopanib is one of the TKIs and is considered a first-line treatment for adult patients with metastatic renal cell carcinoma. Many endocrine-related adverse effects have been noted with the use of TKIs including hypothyroidism, vitamin D deficiency, altered bone density, secondary hyperparathyroidism, abnormal glucose metabolism, gynecomastia, and hypogonadism. Subclinical glucocorticoid deficiency and adrenal insufficiency have been reported with the use of TKIs in only a few cases so far; thus, its true prevalence and clinical significance have yet to be fully elucidated. The mechanism is still not fully understood; however, adrenal toxicity with hemorrhage and/or necrosis of the adrenal glands has been observed in studies. In this article, we describe the first reported case of pazopanib inducing primary adrenal insufficiency in a patient with metastatic renal cell carcinoma diagnosed after the exclusion of all other causes of primary adrenal insufficiency.
酪氨酸激酶抑制剂 (TKI) 已被用于多种类型癌症的治疗。帕唑帕尼是一种 TKI,被认为是转移性肾细胞癌成年患者的一线治疗药物。使用 TKI 可引起许多与内分泌相关的不良反应,包括甲状腺功能减退、维生素 D 缺乏、骨密度改变、继发性甲状旁腺功能亢进、葡萄糖代谢异常、男性乳房发育和性腺功能减退。到目前为止,只有少数病例报道了使用 TKI 会导致亚临床糖皮质激素缺乏和肾上腺功能不全;因此,其真正的患病率和临床意义尚未完全阐明。其机制尚不完全清楚;然而,在研究中观察到了肾上腺出血和/或坏死引起的肾上腺毒性。在本文中,我们描述了首例转移性肾细胞癌患者在排除所有其他原发性肾上腺功能不全的原因后被诊断为帕唑帕尼引起原发性肾上腺功能不全的病例。