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. 2023 Mar 11;7(15):3806–3815. doi: 10.1182/bloodadvances.2022008414

Table 4.

AEs, regardless of relationship to study treatment (≥30% of patients with BRAF V600–mutant LCH in either study)

Category CDRB436A2102 (dabrafenib monotherapy) (n = 13)
CTMT212X2101 (dabrafenib + trametinib) (n = 12)
Any grade Grade ≥3 Any grade Grade ≥3
Any AE, n (%) 13 (100) 11 (84.6) 12 (100) 9 (75.0)
 Pyrexia 9 (69.2) 3 (23.1) 10 (83.3) 4 (33.3)
 Vomiting 9 (69.2) 0 9 (75.0) 0
 Cough 8 (61.5) 0 7 (58.3) 0
 Dry skin 6 (42.6) 0 6 (50.0) 0
 Upper respiratory tract infection 6 (46.2) 0 6 (50.0) 1 (8.3)
 Headache 5 (38.5) 0 2 (16.7) 0
 Hypophosphatemia 5 (38.5) 0 3 (25.0) 0
 Blood creatinine increased 5 (38.5) 0 3 (25.0) 0
 Constipation 5 (38.5) 0 2 (16.7) 0
 WBC count decreased 5 (38.5) 0 1 (8.3) 0
 Nausea 4 (30.8) 1 (7.7) 3 (25.0) 0
 Conjunctivitis 4 (30.8) 1 (7.7) 2 (16.7) 0
 Rash 4 (30.8) 0 2 (16.7) 0
 Diarrhea 4 (30.8) 0 6 (50.0) 0
 Melanocytic naevus 4 (30.8) 0 0 0
 Anemia 4 (30.8) 0 2 (16.7) 1 (8.3)
 Rhinitis 4 (30.8) 0 0 0
 Rhinorrhea 4 (30.8) 0 1 (8.3) 0
 Nasal congestion 4 (30.8) 0 4 (33.3) 0
 Arthropod bite 4 (30.8) 0 0 0
 Maculopapular rash 2 (15.4) 0 6 (50.0) 0
 Abdominal pain 2 (15.4) 0 5 (41.7) 0
 Neutrophil count decreased 2 (15.4) 1 (7.7) 5 (41.7) 3 (25.0)
 AST increased 3 (23.1) 0 4 (33.3) 1 (8.3)
 Fatigue 3 (23.1) 0 4 (33.3) 0
 Pain in extremities 3 (23.1) 0 4 (33.3) 0

AST, aspartate aminotransferase; WBC, white blood cell.