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. 2018 Nov 14;30(2):317–324. doi: 10.1093/annonc/mdy500

Table 3.

Incidence of treatment-related adverse events

AEs Paclitaxel (n =38) Paclitaxel+trametinib (n =36) Paclitaxel+pazopanib (n =37)
n (%)
Any grade AEs 36 (95) 36 (100) 37 (100)
Grade ≥3 AEs 9 (24) 27 (75) 29 (78)
Fatal AEs 0 (0) 1 (4) 2 (5)
AE per patient for AEs affecting 15 or more patientsa,b n (n of grade 3 or more)
Rash 6 (0) 35 (14) 9 (0)
ALT increased 1 (0) 2 (0) 12 (9)
Fatigue 19 (1) 24 (4) 18 (3)
Dyspnoea 8 (1) 10 (1) 8 (2)
Abdominal pain 7 (0) 11 (1) 14 (2)
Diarrhoea 17 (0) 24 (2) 20 (1)
Nausea 11 (0) 12 (0) 16 (1)
Anaemia 3 (0) 6 (2) 8 (0)
Alopecia 17 (1) 13 (0) 13 (0)
Anorexia 6 (0) 13 (0) 11 (0)
Constipation 11 (0) 13 (0) 2 (0)
Dysgeusia 3 (0) 4 (0) 12 (0)
Dyspepsia 7 (0) 4 (0) 4 (0)
Epistaxis 4 (0) 9 (0) 6 (0)
Headache 2 (0) 6 (1) 7 (0)
Vomiting 6 (0) 5 (0) 9 (0)
Cough 8 (0) 5 (0) 5 (0)
a

The AE terms are ranked according to the highest frequency of grade ≥3.

b

In any one row, a patient appears only once whether they had one episode of the AE or many.

AE, adverse events measured by Common Terminology Criteria for Adverse Events V4.03; ALT, alanine aminotransferase; n, number of patients in a group.