The utilization of immunotherapy and targeted therapies in advanced malignancies is rapidly increasing due to advancing technologies. While highly effective, the unintended toxicities and immune-related adverse events (irAEs) associated with these treatments require vigilant monitoring. Autoimmune hypophysitis and subsequent pituitary dysfunction represent critical complications of immune checkpoint inhibitors (ICIs), particularly pembrolizumab. Hypopituitarism can manifest as panhypopituitarism leading to a life-threatening secondary adrenal crisis or as selective anterior pituitary hormone deficiencies, such as isolated adrenocorticotropic hormone (ACTH) or gonadotropin deficiency. We report the case of a 73-year-old man with recurrent melanoma who presented with pituitary dysfunction secondary to pembrolizumab therapy. This case highlights the necessity of investigating, screening, and promptly treating new constitutional symptoms in patients undergoing ICI therapy, as these endocrine complications can be fatal if left unrecognized.
Thu et al. (Sun,) studied this question.
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