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. 2023 Apr 14;13:1154246. doi: 10.3389/fonc.2023.1154246

Table 2.

Adverse events of BRAFi and MEKi monotherapy reported in glioma trials.

BRAFi MEKi
Dabrafenib (23) Vemurafenib (25) Selumetinib (141) Trametinib (143)
Toxicity Any (%) Grade >=3 Toxicity Any (%) Grade >=3 Toxicity Grades 1–2 (%) Grade >=3 Toxicity Any (%) Grade >=3
Fatigue 34 0 Arthralgia 67 0 CK elevated 68 10 Any 89 44
Rash 31 0 Melanocytic nevus 38 0 Hypoalbuminaemia 62 0 Rash 38 11
Dry skin 28 0 PPES 38 0 Dyspnea 60 0 Paronychia 38 6
Pyrexia 28 0 Alopecia 33 0 Duodenal ulcer 58 0 Xerodermia 22 0
Rash maculopapular 28 9 Fatigue 29 4 Rash 58 10 Diarrhea 11 0
Arthralgia 25 3 Pruritis 29 0 Dry skin 56 0 Dizziness 11 0
Headache 22 0 Rash 29 13 Fatigue 56 0 Eczema 11 6
Vomiting 22 0 Folliculitis 25 0 Anemia 56 0 Fatigue 11 0
Arthralgia 3 3 Headache 25 0 Diarrhea 54 4 Oral mucositis 11 0
DIC 3 3 Constipation 21 0 Vomiting 44 0 Left ventricular dysfunction 6 0
EF decreased 3 0 Diarrhea 21 0 Paronychia 38 6 Pancreatitis 6 6
Hypotension 3 3 Nausea 21 0 EF decreased 38 2 Constipation 6 0

CK, creatinine phosphokinase; DIC, disseminated intravascular coagulation; EF, ejection fraction; PPES, palmar-planar erythrodysesthesia.