Table 1.
Vemurafenib*$ | Dabrafenib‡ | Trametinib§ | Dabrafenib + trametinib‖¶# | |
---|---|---|---|---|
Rash | 41 (9) | 30 (0) | 57 (8) | 27 (0) |
Cutaneous SCC | 19 (19) | 10 (4) | 0 | 7 (5) |
Diarrhoea | 25 (<1) | NR | 43 (0) | 36 (2) |
Pyrexia | NR | 16 (3) | NR | 51 (6) |
Arthralgia | 56 (6) | 19 (<1) | NR | 24 (0) |
Fatigue | 46 (3) | 18 (1) | 26 (4) | 53 (4) |
Cardiac | NR | NR | 7 (1) | 9 (0) |
ILD/pneumonitis | NR | NR | 2 (2) | 1 |
Ophthalmologic | NR | NR | 9 (<1) | 2 (2) |
Hypertension | NR | 4 (0) | 15 (12) | 9 (2) |
Hyperglycaemia | NR | 49 (2)# | NR | 58 (5) |
Liver laboratory abnormalities: | 36 (11) | 26 (2) # | 24 (2) | 60 (2) |
Alkaline phosphatase | 11 (0) # | 39 (3) | 42 (4) | |
Alanine aminotransferase | 0 (0) # | NR | 15 (0) | |
Bilirubin | 60 (2)# | 60 (2) | 60 (5) | |
Aspartate aminotransferase |
Toxicities are expressed as percentage of all CTC grades (CTC grade 3/4). The data in this table are summarized from different trials and do not represent direct comparisons.
Data are a composite of phase I/II and III trial data since limited data are available from the phase III trial.
SCC, squamous cell carcinoma; ILD, interstitial lung disease; NR, not reported.