Elevated CK from immune checkpoint inhibitor- related hypophysitis: a case report

被引:0
作者
Gill, Jasmine [1 ]
Walker, John [2 ]
Ye, Carrie [1 ,3 ]
机构
[1] Univ Alberta, Fac Med & Dent, 8-130 Clin Sci Bldg,11350 83 Ave NW, Edmonton, AB T6G 2G3, Canada
[2] Univ Alberta, Edmonton, AB, Canada
[3] Univ Alberta, Dept Med, Div Rheumatol, Edmonton, AB, Canada
关键词
Adrenal insufficiency; elevated creatine kinase; myositis; combination immunotherapy; nivolumab; ipilimumab; RHABDOMYOLYSIS;
D O I
10.1080/1120009X.2024.2359838
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Immune checkpoint inhibitors (ICIs), have emerged to the forefront of management for various advanced cancers, such as melanoma, lung cancer and renal cell carcinoma. Immune checkpoints such as CTLA-4 and PD-1 serve to inhibit T cell activation and signaling; therefore through blockade of these pathways, ICIs promote anti-tumour immune activation. However, as a result of T cell disinhibition, ICIs have been reported to cause immune related adverse events (irAEs) affecting numerous organ systems. One of the most serious and potentially life-threatening irAE is inflammatory myositis. Myositis, which generally presents with progressive proximal muscle weakness and elevated serum creatine kinase (CK), has been reported in <1% of patients who have received ICI therapy. A rare cause of elevated CK is adrenal insufficiency, which has been reported in up to 6% of ICI users. Here we report a case of ICI-related hypophysitis related myopathy that was initially misdiagnosed as ICI-associated inflammatory myositis. This case illustrates the importance of considering a wide differential when assessing hyperCKemia in the setting of ICI use.
引用
收藏
页码:372 / 375
页数:4
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