Division of Endocrinology, Department of Medicine and Research Center, Centre hospitalier de l'Université de Montréal (CRCHUM), Montreal, Quebec, H2X 3E4, Canada.
Service d'Endocrinologie, Maladies métaboliques et Nutrition, Pôle Cardio-Vasculaire et Métabolique, Centre Hospitalo-Universitaire de Toulouse, 31059 Toulouse Cedex, France.
J Clin Endocrinol Metab. 2023 Aug 18;108(9):2336-2342. doi: 10.1210/clinem/dgad115.
Central hypothyroidism was described previously in mitotane-treated patients but data on its prevalence and time of occurrence are limited.
To better characterize thyroid hormone insufficiency in patients exposed to mitotane.
We reviewed medical records of patients from 2 academic centers in Montreal (Canada) and Toulouse (France) with exposure to mitotane therapy for adrenocortical cancer between 1995 and 2020. We analyzed the thyroid function parameters during and after treatment.
In our cohort of 83 patients, 17 were excluded because of preexisting primary hypothyroidism or drug-induced hypothyroidism. During follow-up, 3/66 patients maintained a normal thyroid function and 63/66 developed central hypothyroidism. Among those 63 patients, 56 presented with an inappropriately normal or low TSH and 7 with a mildly elevated TSH. The onset of hypothyroidism was: <3 months in 33.3%, 3 to 6 months in 19.1%, 6 to 9 months in 14.3%, and 9 to 12 months in 9.5%. At least 14.3% of cases occurred after 12 months of exposure, and 6 patients had an undetermined time of occurrence. Over time, 27 patients stopped mitotane and partial (42.3%) or complete (23.1%) recovery from hypothyroidism was observed, mainly in the first 2 years after mitotane discontinuation.
Mitotane therapy is frequently associated with new onset of central hypothyroidism with a prevalence of 95.5%. Most cases occurred in the first year of treatment. Partial or full recovery of thyroid function occurs in 65.4% of cases. This study supports the importance of systematic monitoring of TSH and free T4 levels during and following discontinuation of mitotane therapy.
先前曾在接受米托坦治疗的患者中描述过中枢性甲状腺功能减退症,但有关其患病率和发生时间的数据有限。
更好地描述暴露于米托坦的患者的甲状腺激素不足。
我们回顾了 1995 年至 2020 年间在加拿大蒙特利尔和法国图卢兹的 2 个学术中心接受米托坦治疗的肾上腺皮质癌患者的病历。我们分析了治疗期间和治疗后的甲状腺功能参数。
在我们的 83 名患者队列中,有 17 名患者因存在原发性甲状腺功能减退症或药物引起的甲状腺功能减退症而被排除在外。在随访期间,3/66 名患者保持正常的甲状腺功能,63/66 名患者发生中枢性甲状腺功能减退症。在这 63 名患者中,56 名患者的 TSH 水平异常正常或降低,7 名患者的 TSH 水平轻度升高。甲状腺功能减退症的发病时间为:<3 个月占 33.3%,3-6 个月占 19.1%,6-9 个月占 14.3%,9-12 个月占 9.5%。至少有 14.3%的病例发生在暴露于米托坦 12 个月后,6 例患者的发病时间不确定。随着时间的推移,27 名患者停止了米托坦治疗,观察到部分(42.3%)或完全(23.1%)甲状腺功能减退症恢复,主要发生在停用米托坦后的前 2 年。
米托坦治疗常伴有新发生的中枢性甲状腺功能减退症,患病率为 95.5%。大多数病例发生在治疗的第一年。65.4%的病例出现甲状腺功能部分或完全恢复。本研究支持在米托坦治疗期间和治疗后系统监测 TSH 和游离 T4 水平的重要性。