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. Author manuscript; available in PMC: 2020 Aug 1.
Published in final edited form as: Clin Breast Cancer. 2019 Mar 6;19(4):225–235.e2. doi: 10.1016/j.clbc.2019.02.010

Table 4.

Joint analysis of GATA3 single nucleotide polymorphisms and breast cancer outcomes in the S8897 trial and Pathways Study

Genotype # events/patients Adjusted HR (95% CI) Adjusted P
A. Overall survival
rs3802604
  AA 34/261 1.00
  GA 44/368 0.98 (0.62-1.53) 0.92
  GG 23/122 1.59 (0.94-2.71) 0.09
 Per risk allele 1.23 (0.93-1.63) 0.15
rs568727
  CC 39/290 1.00
  AC 37/364 0.71 (0.45-1.11) 0.13
  AA 25/96 1.86 (1.11-3.12) 0.02
 Per risk allele 1.26 (0.94-1.68) 0.13

B. Disease-free survival
rs3802604
  AA 52/261 1.00
  GA 71/368 0.96 (0.67-1.38) 0.84
  GG 33/122 1.49 (0.96-2.30) 0.08
 Per risk allele 1.18 (0.94-1.49) 0.15
rs568727
  CC 57/290 1.00
  AC 66/364 0.85 (0.59-1.21) 0.37
  AA 33/96 1.80 (1.16-2.79) 0.009
 Per risk allele 1.25 (0.98-1.59) 0.07

Footnote: Hazard ratios (HRs), 95% confidence intervals (CIs) and p-values were derived from Cox hazard regression models with adjustment for study, age at enrollment, race and ethnicity, and treatment arms. Estimates of per risk allele were derived from an additive genetic model by treating genotypes as 0, 1 and 2 according to the copy number of risk allele.