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. 2011 Feb 1;104(4):559–563. doi: 10.1038/bjc.2011.4

Table 1. Comparison of clinical characteristics between the ‘control’ and the ‘prophylactic lamivudine’ groups in the HBsAg-positive breast cancer patients.

  Control group Prophylactic lamivudine group  
  N % N % P-value
No. of patients 76 58 55 42  
           
Age (years) median, range 46 (30–69)   48 (30–68)   0.18
           
Pre-chemotherapy status
 AST (IU l−1) (0–40)a, mean 24   30   0.09
 ALT (IU l−1) (0–40)a, mean 25   25   0.25
 Total bilirubin (mg dl−1) (0.2–1.5)a, mean 0.5   0.6   0.11
 Albumin (g dl−1) (3.5–5.2)a, mean 4.2   4.0   0.06
           
Chemotherapy regimen
 AC 17 22 3 5  
 FAC 28 37 25 45 0.02
 AC → D/T 31 41 27 50  
           
Steroid use for anti-emetics 33 45 28 51 0.48
           
Stage
 1 11 15 9 16  
 2 39 51 32 58 0.56
 3 26 34 14 26  
           
Adjuvant RT 12 16 4 7 0.18

Abbreviations: AC=doxorubicin + cyclophosphamide; AC → D/T=AC followed by docetaxel or paclitaxel; ALT=alanine-aminotransferase; AST=aspartate aminotransferase; FAC=5-FU + doxorubicin + cyclophosphamide; HbsAg=hepatitis B virus surface antigen; RT=radiation therapy.

a

Normal range.