2013
DOI: 10.1089/thy.2013.0241
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Thyroid Dysfunction as an Unintended Side Effect of Anticancer Drugs

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Cited by 99 publications
(81 citation statements)
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References 236 publications
(228 reference statements)
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“…Although Hashimoto disease was described as a risk factor for papillary thyroid cancer, in the current study Hashimoto disease and thyroid cancer did not occur more frequently in the same patients [21,22].…”
Section: Discussioncontrasting
confidence: 68%
“…Although Hashimoto disease was described as a risk factor for papillary thyroid cancer, in the current study Hashimoto disease and thyroid cancer did not occur more frequently in the same patients [21,22].…”
Section: Discussioncontrasting
confidence: 68%
“…However, no biopsyproven ipilimumab-or nivolumab-induced AH has been reported [12]. In addition, the prevalence of anti-pituitary antibodies remains unknown in large cohorts of patients with immune-checkpoint inhibitorinduced hypophysitis, although endocrine irAEs such as destructive thyroiditis and fulminant type I diabetes mellitus have been reported in patients treated with immune-checkpoint blocking agents [9,17]. Ricciuti A et al recently reported that the human pituitary gland was the best substrate to detect anti-pituitary antibodies by indirect immunofluorescence [18].…”
Section: Discussionmentioning
confidence: 99%
“…In addition to these evidence-based immune-mediated anti-cancerous effects, ipilimumab frequently induces several endocrine immune-related adverse events (irAEs) such as hypophysitis and destructive thyroiditis as a consequence of enhanced T cell functions [8][9][10][11][12]. Although hypophysitis induced by nivolumab has also been reported, its incidence in Western countries appears to be lower than that observed with ipilimumab [12].…”
mentioning
confidence: 99%
“…The function of the thyroid gland can be adversely impacted at various levels of the HPT axis by systemic therapies that are prescribed for the treatment of cancer [102] (Table 1). Although much better described in adults, these off-target consequences of cancer therapy will likely become more commonplace in children, given the expanding role of TKIs and immune checkpoint inhibitors in the pediatric oncology field [103, 104].…”
Section: Thyroid Dysfunction Due To Non-radioactive Systemic Therapiesmentioning
confidence: 99%
“…First described with the drug sunitinib [105], de novo primary thyroid disease can occur with many of the commercially available TKIs [102, 106-109] (Table 1). Several mechanisms for TKI-induced thyroid dysfunction have been proposed, including induction of destructive thyroiditis, inhibition of thyroid peroxidase activity, effects on thyroid hormone absorption and clearance, impaired iodide uptake, and thyroid capillary regression caused by vascular endothelial growth factor inhibition [102, 106, 107]. Destructive thyroiditis is likely a major mechanism, and this follows a typical pattern of hyperthyroidism followed by hypothyroidism [102, 110, 111].…”
Section: Thyroid Dysfunction Due To Non-radioactive Systemic Therapiesmentioning
confidence: 99%