Sharaf Mayesha, Shah Pinak
Department of Internal Medicine, Mountain View Hospital, Sunrise Health GME Consortium, HCA Healthcare, Las Vegas, Nevada.
AACE Endocrinol Diabetes. 2025 Apr 10;12(1):54-56. doi: 10.1016/j.aed.2025.02.007. eCollection 2025 May-Jun.
BACKGROUND/OBJECTIVE: Lenvatinib and pembrolizumab are emerging agents being used for various malignant tumors with antitumor activity and an acceptable safety profile. However, monotherapy with these immunotherapies can lead to various endocrinopathies, which raises an important question-whether the combination increases the risk of endocrinopathy even further and even after discontinuation. The objective of this report is to describe a case of development of hypothyroidism 13 weeks following discontinuation of the combined immunotherapy lenvatinib and pembrolizumab.
A 75-year-old man was started on lenvatinib and pembrolizumab after he was found to have metastatic renal cell carcinoma. He was diagnosed with subclinical hypothyroidism following 1 month of treatment, which resolved spontaneously with normalization of thyroid-stimulating hormone level. The immunotherapies were discontinued after 8 months. He presented with generalized weakness, failure to thrive, and poor oral intake 3 months following discontinuation of immunotherapies and was diagnosed with hypothyroidism as laboratory workup revealed a thyroid-stimulating hormone level of >150 mIU/mL (normal range, 0.5-5.0 mIU/mL) and free thyroxine level of 0.17 ng/dL (normal range, 0.9-1.7 ng/dL).
Both lenvatinib and pembrolizumab can cause hypothyroidism and should be considered even after discontinuation of the immunotherapies. Keeping a broad differential is key to early diagnosis and treatment initiation and to reduce mortality and morbidity associated with hypothyroidism.
Although adverse endocrine toxicities are common with immunotherapy with lenvatinib-pembrolizumab, development of such adverse reactions following discontinuation of the combined chemotherapy is rare. Our case represents hypothyroidism as late as 3 months after the discontinuation of immunotherapies.
背景/目的:乐伐替尼和帕博利珠单抗是用于多种恶性肿瘤的新型药物,具有抗肿瘤活性且安全性可接受。然而,这些免疫疗法单药治疗可导致各种内分泌病,这就引出了一个重要问题——联合使用是否会进一步增加内分泌病风险,甚至在停药后也是如此。本报告的目的是描述一例在停用乐伐替尼和帕博利珠单抗联合免疫治疗13周后发生甲状腺功能减退的病例。
一名75岁男性在被发现患有转移性肾细胞癌后开始使用乐伐替尼和帕博利珠单抗治疗。治疗1个月后,他被诊断为亚临床甲状腺功能减退,随着促甲状腺激素水平恢复正常,该症状自行缓解。8个月后停用免疫疗法。在停用免疫疗法3个月后,他出现全身无力、生长发育迟缓及食欲不佳,实验室检查显示促甲状腺激素水平>150 mIU/mL(正常范围0.5 - 5.0 mIU/mL),游离甲状腺素水平为0.17 ng/dL(正常范围0.9 - 1.7 ng/dL),被诊断为甲状腺功能减退。
乐伐替尼和帕博利珠单抗均可导致甲状腺功能减退,即使在停用免疫疗法后也应予以考虑。保持广泛的鉴别诊断对于早期诊断、开始治疗以及降低与甲状腺功能减退相关的死亡率和发病率至关重要。
尽管乐伐替尼 - 帕博利珠单抗免疫治疗常见不良内分泌毒性,但联合化疗停药后出现此类不良反应较为罕见。我们的病例代表了免疫治疗停药后3个月才出现甲状腺功能减退。