ArticleCureus2024
Elevated Creatine Kinase (CK) and Myositis Triggered by Immune Checkpoint Inhibitors: Muscle Mysteries Unveiled.
Article in Cureus, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
1 citing paper in PubMed.
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Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Immune checkpoint inhibitors (ICIs), including programmed cell death protein 1 (PD-1) inhibitors, such as nivolumab, and cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) inhibitors, such as ipilimumab, have revolutionized cancer treatment, particularly in metastatic melanoma. However, these therapies can cause immune-related adverse events (irAEs), including myositis, a rare but significant complication characterized by elevated creatine kinase (CK) and muscle weakness. We present the case of a 79-year-old male with a history of metastatic melanoma to the brain, previously treated with nivolumab and ipilimumab, who was admitted after an unwitnessed fall. Initial laboratory tests revealed significantly elevated CK levels (5277 U/L) and mildly elevated liver function tests (LFTs). Despite the absence of muscle pain or weakness upon presentation, the patient developed proximal muscle weakness and myalgias during hospitalization. Extensive workup, including negative autoimmune panels and imaging, raised suspicion of immune-related myositis given the recent ICI therapy. The patient was treated with prednisone, which resulted in a rapid decrease in CK levels and improvement of symptoms, supporting the diagnosis of ICI-related myositis.
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