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Melanoma Res ; 32(4): 299-301, 2022 08 01.
Article in English | MEDLINE | ID: mdl-35635528

ABSTRACT

The effect of serine/threonine-protein kinase B-Raf/mitogen-activated protein kinase (BRAF/MEK) inhibitors on the immune system is not clearly described, but rare cases of autoimmune phenomena have been reported. The clinical case we present below is the first report of a necrotizing myopathy related to dabrafenib/trametinib treatment. A 48-year-old man started dabrafenib/trametinib for stage IV BRAF-V600E mutated cutaneous melanoma. After the first month, he presented with grade 3 pyrexia (Common Terminology Criteria for Adverse Events [CTCAE] v.5.0.) and increased creatinine-kinase levels. A diagnosis of immune-mediated necrotizing myopathy, antisignal recognition particle (anit-SRP) positive, was made. At disease progression, dabrafenib/trametinib was restarted, triggering a new episode of grade 2 pyrexia and myositis. Treatment was changed to encorafenib/binimetinib without repeating pyrexia or limiting creatinine-kinase elevation, presenting even a loss of anti-SRP antibodies. Given the temporal relationship, the fact that re-exposition induced a new worsening of the myopathy and the loss of the anti-SRP antibodies after changing treatment, we infer that there possibly is a clear relationship between dabrafenib/trametinib treatment and the myopathy.


Subject(s)
Melanoma , Myositis , Skin Neoplasms , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Creatinine/therapeutic use , Fever/etiology , Humans , Imidazoles/adverse effects , Male , Melanoma/etiology , Middle Aged , Mitogen-Activated Protein Kinase Kinases , Mutation , Myositis/chemically induced , Oximes/adverse effects , Protein Kinase Inhibitors/adverse effects , Proto-Oncogene Proteins B-raf/genetics , Pyridones , Pyrimidinones/adverse effects , Skin Neoplasms/etiology
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