Table 3 |
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|
British Columbia Randomized Radiation trial, 2005 update |
||
| Hazard ratio |
95% confidence interval |
|
|
|
||
| DFS |
||
| All patients |
0.63 |
0.47 to 0.83 |
| N1 to N3 |
0.64 |
0.42 to 0.97 |
| N4+ |
0.59 |
0.38 to 0.91 |
| SysDFS |
||
| All patients |
0.66 |
0.49 to 0.88 |
| N1 to N3 |
0.68 |
0.45 to 1.04 |
| N4+ |
0.63 |
0.41 to 0.97 |
| Overall survival |
||
| All patients |
0.73 |
0.55 to 0.98 |
| N1 to N3 |
0.76 |
0.50 to 1.15 |
| N4+ |
0.63 |
0.41 to 0.97 |
|
|
||
|
Cyclophosphamide methotrexate, 5-fluoracil + radiation versus cyclophosphamide methotrexate, 5-fluoracil alone, including all patients and involving patients with one to three axillary nodes involved (N1 to N3) and patients with four or more axillary nodes involved (N4+). DFS, first event breast cancer recurrence (or any death); SysDFS, DFS with systemic recurrence as a first event. Adapted from Ragaz and colleagues [12]. |
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|
Ragaz Breast Cancer Research 2009 11(Suppl 3):S14 doi:10.1186/bcr2433 |
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