Approach to the Patient With Thyroid Nodules: Considering GLP-1 Receptor Agonists

被引:0
|
作者
Kelly, Clare A. [1 ]
Sipos, Jennifer A. [2 ]
机构
[1] Univ Hosp Cleveland Med Ctr, Div Endocrinol, Cleveland, OH 44106 USA
[2] Ohio State Univ, Wexner Med Ctr, Div Endocrinol, 77 McCampbell Hall,1851 Dodd Dr, Columbus, OH 43210 USA
关键词
thyroid cancer; calcitonin; medullary thyroid cancer; differentiated thyroid cancer; glucagon-like peptide 1; glucagon-like peptide 1 receptor agonist; GLUCAGON-LIKE PEPTIDE-1; PANCREATIC-CANCER CELLS; C-CELLS; CALCITONIN CONCENTRATIONS; INHIBITS GROWTH; IN-VIVO; LIRAGLUTIDE; EXENATIDE; INSULIN; PROLIFERATION;
D O I
10.1210/clinem/dgae722
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Glucagon-like peptide 1 receptor agonists (GLP1RAs) have rapidly changed the landscape of diabetes and obesity treatment. Enthusiasm for their use is tempered with concerns regarding their risk for inducing C-cell tumors based on preclinical studies in rodents. A black-box warning from the US Food and Drug Administration recommends against using GLP1RA in patients with a personal or family history of medullary thyroid carcinoma (MTC) or multiple endocrine neoplasia syndrome type 2A or 2B (MEN2), providing clear guidance regarding this cohort of patients. However, emerging data also suggest an increased incidence of differentiated thyroid cancer (DTC) in patients treated with these agents. Other studies, though, have not confirmed an association between GLP1RAs and DTC. With conflicting results concerning thyroid cancer risk, there is no clear consensus regarding the optimal approach to screening patients prior to initiating the medications and/or evaluating for thyroid cancer during GLP1RA treatment. Within the context of patient cases, this review will summarize the existing data, describe ongoing controversies, and outline future areas for research regarding thyroid cancer risk with GLP1RA use.
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页数:8
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