阿帕鲁胺对前列腺癌患者甲状腺功能的影响

IF 3 Q2 ENDOCRINOLOGY & METABOLISM Journal of the Endocrine Society Pub Date : 2024-05-27 eCollection Date: 2024-05-23 DOI:10.1210/jendso/bvae105
Clare Moffatt, Melissa G Lechner, Trevor E Angell, John Shen, Alexandra Drakaki, Gonzalo J Acosta, Tom Z Liang, Karen Tsai
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引用次数: 0

摘要

背景:阿帕鲁胺(APT)是一种非甾体抗雄激素药物,用于治疗转移性阉割敏感性前列腺癌和非转移性阉割耐药前列腺癌。早期的 APT 临床试验发现,甲状腺功能障碍是治疗过程中常见的不良反应,但 APT 引起的甲状腺功能减退的临床表现和处理方法尚未得到研究:我们的研究旨在阐明前列腺癌患者APT相关甲状腺功能障碍的临床表现和治疗方法:我们报告了两个学术医疗中心的16例前列腺癌治疗期间APT相关甲状腺功能障碍患者的病例系列。我们对患者的临床参数、甲状腺功能实验室数据以及 APT 治疗过程中的甲状腺激素需求量进行了分析:结果:在我们的 16 例 APT 相关甲状腺功能减退症患者中,3 例之前没有甲状腺疾病,13 例之前存在甲状腺功能减退症。甲状腺功能障碍的模式包括显性和亚临床甲减。从开始使用 APT 到甲状腺功能检测出现异常的中位时间为 19 周,但有些病例早在 2 到 4 周前就出现了甲状腺功能异常。使用左甲状腺素(LT4)替代甲状腺激素可有效控制甲状腺功能减退症,但一些原有甲状腺功能减退症的患者需要在服用 APT 期间将剂量增加 2 到 3 倍才能达到甲状腺功能正常状态。在完成或停止APT治疗的患者中,促甲状腺激素水平在APT治疗后11周内中位下降,甲状腺激素需求量也降至接近APT治疗前的水平:结论:APT相关甲状腺功能障碍表现为新的或恶化的甲状腺功能减退,应及时开始或增加甲状腺激素替代治疗。建议对所有 APT 患者每 1 到 2 个月进行一次甲状腺功能检测,并在 APT 治疗结束后 2 到 3 个月进行一次检测。
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The Effect of Apalutamide on Thyroid Function in Prostate Cancer Patients.

Context: Apalutamide (APT) is a nonsteroidal antiandrogen medication used to treat metastatic castrate-sensitive and nonmetastatic castrate-resistant prostate cancer. Early clinical trials of APT identified thyroid dysfunction as a common adverse effect of therapy, but the clinical presentation and management of APT-induced hypothyroidism has not been studied.

Objective: The objective of our study is to elucidate the clinical presentation and treatment approach of APT-associated thyroid dysfunction in prostate cancer patients.

Methods: We report a case series of 16 patients with APT-associated thyroid dysfunction during prostate cancer treatment at 2 academic medical centers. Patient clinical parameters, thyroid function laboratory data, and thyroid hormone requirements over the course of APT treatment were analyzed.

Results: Among the 16 patients in our case series with APT-associated hypothyroidism, 3 had no prior thyroid disease and 13 had preexisting hypothyroidism. The patterns of thyroid dysfunction included overt and subclinical hypothyroidism. The median time from APT initiation to thyroid function test abnormality was 19 weeks, but occurred in some cases as early as 2 to 4 weeks. Hypothyroidism was effectively managed with thyroid hormone replacement using levothyroxine (LT4), though some patients with preexisting hypothyroidism required a 2- to 3-fold dose increase while on APT to achieve a euthyroid state. In the subset of patients who completed or stopped APT therapy, thyrotropin levels fell at a median of 11 weeks post APT therapy and thyroid hormone requirements decreased to near pre-APT levels.

Conclusion: APT-associated thyroid dysfunction presents as new or worsening hypothyroidism and should prompt initiation or increase in thyroid hormone replacement. Monitoring of thyroid function tests is recommended every 1 to 2 months for all patients on APT and 2 to 3 months after completion of APT.

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来源期刊
Journal of the Endocrine Society
Journal of the Endocrine Society Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
5.50
自引率
0.00%
发文量
2039
审稿时长
9 weeks
期刊最新文献
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