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Table 2 Multivariate analyses of ability of Shc proteins to predict failure of tamoxifen therapy

From: p66 Shc and tyrosine-phosphorylated Shc in primary breast tumors identify patients likely to relapse despite tamoxifen therapy

 

Population cohort

Case-control cohort

Model

HRa (95% CI)

P b

RRa (95% CI)

P b

PY-Shc, p66 Shc

8.6 (2.6–30)

0.001

7.7 (1.4–44)

0.022

PY-Shc, p66 Shc

    

   Adjusted for nodal status

8.3 (1.8–38)

0.007

12.1 (1.7–86)

0.013

  1. aHR (interquartile) is the RR of relapse comparing patients in the 75th percentile of PY-Shc and 25th percentile of p66 Shc to patients in the 25th percentile of PY-Shc and 75th percentile of p66 Shc. The multivariate Cox model containing PY-Shc and p66 Shc was adjusted for nodal status, AJCC (American Joint Committee on Cancer) stage (population-based cohort), tumor stage, tumor grade, progesterone receptor status, and patient age at diagnosis. bSignificance using Wald statistic. CI, confidence interval; HR, hazard ratio; PY-Shc, tyrosine-phosphorylated Shc; RR, relative risk.