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. Author manuscript; available in PMC: 2014 Dec 1.
Published in final edited form as: Pharmacogenomics J. 2013 Sep 3;14(3):241–247. doi: 10.1038/tpj.2013.32

Table 1. Descriptive characteristics of breast cancer patients enrolled in the S0221 trial with assessed toxicity by the availability of DNA at the time of genotyping.

Variable Patients with DNA available (n=882) Patients without DNA available (n=1,180)
Age, years, mean ± standard deviation 50.0 ± 10.2 50.4 ± 9.9
Self-reported race, N (%)
European American 734 (83) 921 (78)
African American 69 (8) 149 (13)
Asian 41 (5) 61 (5)
Other 38 (4) 49 (4)
AC Treatment arm, N (%)
 Arm 1 446 (51) 619 (52)
 Arm 2 436 (49) 561 (48)
CTCAE Grade of hematological toxicity, N (%)
 Grade 0-2 592 (67) 830 (70)
 Grade 3 165 (19) 175 (15)
 Grade 4 125 (14) 175 (15)
CTCAE Grade of gastrointestinal toxicity, N (%)
 Grade 0-2 756 (86) 1004 (85)
 Grade 3 126 (14) 172 (15)
 Grade 4 0 (0) 4 (0)