Yavuz Sahzene, Apolo Andrea B, Kummar Shivaani, del Rivero Jaydira, Madan Ravi A, Shawker Thomas, Reynolds James, Celi Francesco S
1 National Institute of Diabetes and Digestive and Kidney Diseases, Diabetes, Endocrine, and Obesity Branch, National Institutes of Health , Bethesda, Maryland.
Thyroid. 2014 Aug;24(8):1223-31. doi: 10.1089/thy.2013.0621. Epub 2014 Jun 5.
Thyroid dysfunction is a common adverse event associated with tyrosine kinase inhibitors (TKI), but its underlying pathophysiology is unclear. Cabozantinib is a novel TKI currently Food and Drug Administration approved for advanced medullary thyroid cancer and tested in clinical trials on solid tumors including prostate, liver, bladder, breast, and ovarian cancer.
We analyzed the thyroid function of patients enrolled in two phase 2 clinical trials using cabozantinib at the National Institutes of Health Clinical Center. Two cases of thyroiditis associated with cabozantinib therapy are presented in detail, and a systematic review of the literature on TKI-associated thyroid dysfunction is also discussed.
Between September 2012 and September 2013, 33 patients were treated with cabozantinib, and follow-up thyroid function tests were available for 31 (20 males, 11 females; age 59±1 years). Thyroid dysfunction was recorded in the majority of patients (93.1%), with a predominance of subclinical hypothyroidism. Two cases showed a biphasic pattern of thyroid dysfunction characterized by a transient thyrotoxicosis followed by hypothyroidism. Color Doppler demonstrated an increase in vascularization during the thyrotoxic phase, but no uptake was visualized on nuclear medicine imaging. A systematic review of the literature resulted in the identification of 40 original manuscripts, of which 13 were case series and 6 were case reports describing TKI-associated thyroid dysfunction.
TKI therapy often results in clinically significant thyroid dysfunction. Cabozantinib treatment commonly results in thyroid dysfunction varying from subclinical hypothyroidism to symptomatic thyrotoxicosis. Early detection and characterization of cabozantinib-associated thyroid dysfunction and close follow-up are essential to provide adequate management of this common adverse event.
甲状腺功能障碍是与酪氨酸激酶抑制剂(TKI)相关的常见不良事件,但其潜在的病理生理学尚不清楚。卡博替尼是一种新型TKI,目前已获美国食品药品监督管理局批准用于晚期甲状腺髓样癌,并在包括前列腺癌、肝癌、膀胱癌、乳腺癌和卵巢癌在内的实体瘤临床试验中进行了测试。
我们分析了在美国国立卫生研究院临床中心参加两项使用卡博替尼的2期临床试验的患者的甲状腺功能。详细介绍了2例与卡博替尼治疗相关的甲状腺炎病例,并讨论了关于TKI相关甲状腺功能障碍的文献系统评价。
2012年9月至2013年9月期间,33例患者接受了卡博替尼治疗,31例(20例男性,11例女性;年龄59±1岁)有后续甲状腺功能测试结果。大多数患者(93.1%)出现甲状腺功能障碍,以亚临床甲状腺功能减退为主。2例表现为甲状腺功能障碍的双相模式,其特征为短暂性甲状腺毒症后出现甲状腺功能减退。彩色多普勒显示甲状腺毒症期血管增多,但核医学成像未见摄取。文献系统评价共识别出40篇原始手稿,其中13篇为病例系列,6篇为描述TKI相关甲状腺功能障碍的病例报告。
TKI治疗常导致具有临床意义的甲状腺功能障碍。卡博替尼治疗通常导致从亚临床甲状腺功能减退到有症状的甲状腺毒症不等的甲状腺功能障碍。早期发现和明确卡博替尼相关甲状腺功能障碍并密切随访对于妥善处理这一常见不良事件至关重要。