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. 2013 May 7;108(10):1931–1935. doi: 10.1038/bjc.2013.225

Table 1. Patient characteristics (n=1149).

  AC/FACa, n=434 (%) Folfox/Folfirib, n=196 (%) Carboplatin/Gemcitabinec, n=245 (%) Capecitabined, n=274 (%)
Age, years (median, range)
52 (35–75)
58 (26–81)
58 (28–79)
60 (28–82)
Gender
Male 2 (0.05) 113 (58) 126 (51) 108 (39)
Female
432 (99.5)
83 (42)
119 (49)
166 (61)
Race
Chinese 278 (64) 163 (83) 180 (74) 195 (71)
Malay 74 (17) 14 (7) 37 (15) 29 (11)
Indian 32 (7) 8 (4) 8 (3) 11 (4)
Others
50 (12)
11 (6)
20 (8)
39 (14)
Tumour type
Breast 434 (100) 0 60 (24) 127 (46)
– Adjuvant 363 (84) 0 0 (0) 0 (0)
– Metastatic
71 (16)
0
60 (24)
127 (46)
Colon 0 162 (83) 0 (0) 112 (41)
– Adjuvant 0 76 (39) 0 (0) 71 (26)
– Metastatic
0
86 (44)
0 (0)
41 (15)
Lung
0
0 (0)
110 (45)
0 (0)
Others
0
24 (17)
75 (31)
25 (13)
Use of steroids in pre-medication
434 (100)
196 (100)
245 (100)
0 (0)
HBV screen
220 (51)
68 (35)
78 (32)
82 (30)
Screen positive 6/220 (3) 10/68 (15) 5/78 (7) 9/82 (11)
a

FAC: Fluorouracil 500 mg m−2, Doxorubicin 50 mg m−2 and Cyclophosphamide 500 mg m−2 every 3 weeks. AC: Doxorubicin 60 mg m−2 and Cyclophosphamide 600 mg m−2 every 3 weeks.

b

Folfox/Folfiri: Oxaliplatin 85 mg m−2 or Irinotecan 180 mg m−2+Folinic acid 400 mg m−2, Fluorouracil bolus 400 mg m−2, then 2400 mg m−2 as an infusion over 46 h every 2 weeks.

c

Carbo/Gem: Carboplatin (area under the concentration time curve 5), Gemcitabine 1000 mg m−2 day 1, day 8 every 3 weeks.

d

Capecitabine: Capecitabine 1000–1250 mg m−2 days 1–14 every 3 weeks.