Table 1.
6-yr DFS | Hazard Ratio | ||
---|---|---|---|
L+T vs T | |||
T→L vs T | |||
Overall | L+T | 85% | 0.86 (95% CI, 0.74–1.00) |
T→L | 84% | 0.93 (95% CI, 0.81–1.08) | |
T | 82% | ||
Design-1 | L+T | 83% | 0.83 (95% CI, 0.69–1.00) |
T→L | 82% | 0.87 (95% CI, 0.73–1.05) | |
T | 79% | ||
Design-2/2B | L+T | 87% | 0.92 (95% CI, 0.72–1.18) |
T→L | 85% | 1.05 (95% CI, 0.82–1.33) | |
T | 86% | ||
Hormone receptor positive | L+T | 85% | 0.91 (95% CI, 0.75–1.11) |
T→L | 85% | 0.90 (95% CI, 0.74–1.10) | |
T | 83% | ||
Hormone receptor negative | L+T | 84% | 0.80 (95% CI, 0.64–1.00) |
T→L | 82% | 0.97 (95% CI, 0.79–1.20) | |
T | 80% | ||
pN0 | L+T | 91% | 0.91 (95% CI, 0.67–1.22) |
T→L | 90% | 1.02 (95% CI, 0.76–1.36) | |
T | 89% | ||
pN1 | L+T | 87% | 0.78 (95% CI, 0.58–1.05) |
T→L | 87% | 0.76 (95% CI, 0.57–1.02) | |
T | 84% | ||
pN2–3 | L+T | 75% | 0.92 (95% CI, 0.71–1.18) |
T→L | 71% | 1.09 (95% CI, 0.86–1.39) | |
T | 73% |
DFS: disease-free survival
L+T: trastuzumab concurrently with lapatinib
T→L: trastuzumab followed by lapatinib
T: trastuzumab alone