Table 1.
Disease-Free Survival | Overall Survival | ||||||||
---|---|---|---|---|---|---|---|---|---|
N | HR | 95%CI | P * | 5-Yr DFS% ± SE | 25-yr DFS% ± SE | HR | 95%CI | P * | |
Trial III [p+T:Obs] | |||||||||
ER+ | |||||||||
p+T | 45 | 0.65 | 0.42 to 1.00 | 0.05 | 56± 7 | 15± 5 | 0.78 | 0.50 to 1.23 | 0.29 |
Obs | 53 | 30± 6 | 7± 4 | ||||||
ER− | |||||||||
p+T | 30 | 1.08 | 0.63 to 1.85 | 0.77 | 20± 7 | 17± 7 | 1.22 | 0.70 to 2.12 | 0.48 |
Obs | 33 | 30± 8 | 11± 6 | ||||||
Trial III [CMFp+T:Obs] | |||||||||
ER+ | |||||||||
CMFp+T | 58 | 0.62 | 0.41 to 0.92 | 0.02 | 58± 7 | 10± 5 | 0.82 | 0.54 to 1.26 | 0.37 |
Obs | 53 | 30± 6 | 7± 4 | ||||||
ER− | |||||||||
CMFp+T | 19 | 0.49 | 0.25 to 0.97 | 0.04 | 63±11 | 35±11 | 0.68 | 0.34 to 1.38 | 0.29 |
Obs | 33 | 30± 8 | 11± 6 | ||||||
Trial III [CMFp+T:p+T] | |||||||||
ER+ | |||||||||
CMFp+T | 58 | 0.96 | 0.63 to 1.47 | 0.85 | 58± 7 | 10± 5 | 1.07 | 0.67 to 1.69 | 0.78 |
P+T | 45 | 56± 7 | 15± 5 | ||||||
ER− | |||||||||
CMFp+T | 19 | 0.44 | 0.22 to 0.89 | 0.02 | 63± 11 | 35±11 | 0.55 | 0.27 to 1.13 | 0.11 |
P+T | 30 | 20± 7 | 17± 7 | ||||||
Trial III–IV [p+T:Obs] * | |||||||||
ER+ | |||||||||
p+T | 104 | 0.64 | 0.48 to 0.86 | 0.003 | 52± 5 | 11± 3 | 0.72 | 0.53 to 0.98 | 0.04 |
Obs | 100 | 35± 5 | 4± 2 | ||||||
ER− | |||||||||
p+T | 51 | 1.18 | 0.78 to 1.79 | 0.44 | 22± 6 | 10± 4 | 1.30 | 0.84 to 2.01 | 0.23 |
Obs | 50 | 30± 6 | 13± 5 |
stratified by Trial.
Abbreviations: p+T: low-dose prednisone and tamoxifen for one year; CMF: classical cyclophosphamide, methotrexate, 5-fluorouracil for one year; Obs: observation: no adjuvant systemic therapy; ER: estrogen receptor status, HR: hazard ratio, CI: confidence interval, DFS: disease-free survival, OS: overall survival, SE: standard error