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. 2013 Mar 28;13:164. doi: 10.1186/1471-2407-13-164

Table 5.

Summary of most common grade 3 and grade 4 toxicities in the four groups (i.e., reported in ≥5% of patients in any group)

 
Arm A
Arm B
Arm C
Arm D
(N=59)
(N=62)
(N=58)
(N=59)
  G3 G4 G3 G4 G3 G4 G3 G4
Neutropenia
24 (40.7)
22 (37.3)
22 (35.5)
7 (11.3)
15 (25.9)
4 (6.9)
23 (39.0)
11 (18.6)
Leukopenia
15 (25.4)
1 (1.7)
7 (11.3)
3 (4.8)
6 (10.3)
0 (0.0)
6 (10.2)
1 (1.7)
ALT increased
1 (1.7)
0 (0.0)
5 (8.1)
0 (0.0)
8 (13.8)
0 (0.0)
6 (10.2)
0 (0.0)
Diarrhoea
0 (0.0)
2 (3.4)
0 (0.0)
0 (0.0)
4 (6.9)
0 (0.0)
0 (0.0)
0 (0.0)
Myalgia
0 (0.0)
0 (0.0)
4 (6.5)
0 (0.0)
0 (0.0)
0 (0.0)
0 (0.0)
0 (0.0)
Alopecia
4 (6.8)
0 (0.0)
0 (0.0)
0 (0.0)
1 (1.7)
0 (0.0)
1 (1.7)
0 (0.0)
Hepatotoxicitya
0 (0.0)
0 (0.0)
1 (1.6)
0 (0.0)
0 (0.0)
0 (0.0)
3 (5.1)
0 (0.0)
Asthenia
4 (6.8)
0 (0.0)
3 (4.8)
0 (0.0)
5 (8.6)
0 (0.0)
6 (10.2)
1 (1.7)
Fatigue 3 (5.1) 0 (0.0) 3 (4.8) 0 (0.0) 3 (5.2) 0 (0.0) 4 (6.8) 0 (0.0)

Data are number (%) of patient; G = CTC Grade.

aALT are included in hepatotoxicities, but were separately reported by different study investigators.

Arm A: docetaxel and gemcitabine with 3-weekly schedule; Arm B: paclitaxel and gemcitabine with 3-weekly schedule; Arm C: docetaxel and gemcitabine with weekly schedule; Arm D: paclitaxel and gemcitabine with weekly schedule.