Table 3.
Trial name | Median follow-up, y | Sample size | Length of treatment in control arm, y | Length of treatment in experimental arm, y | OR for recurrence | 95% CI | P |
---|---|---|---|---|---|---|---|
ATLAS | 7.6* | 6846 | 5 | 10 | 0.84 | 0.74 to 0.94 | .003 |
aTTom | 9† | 6953‡ | 5 | 10 | 0.84 | 0.74 to 0.95 | .006 |
ECOG E4181/E5181 | 9.6 | 140‖ | 5 | Indefinite | 0.33 | 0.15 to 0.70 | .004 |
NSABP B-14 | 7 | 1172 | 5 | 10 | 1.18 | 0.80 to 1.72 | .41 |
Scottish | 10 | 132§ | 5 | Indefinite | 0.93 | 0.46 to 1.92 | .85 |
Results for estrogen receptor (ER)-positive patients. Mean listed. ATLAS = Adjuvant Tamoxifen Longer Against Shorter; aTTom = Adjuvant Tamoxifen–To Offer More?; CI = confidence interval; ECOG E4141/E5181 = Eastern Cooperative Oncology Group; NSABP B-14 = National Surgical Adjuvant Breast and Bowel Project; OR = odds ratio; Scottish = Scottish adjuvant tamoxifen trial a randomized study updated to 15 years.
Estimated follow-up.
Whole cohort analyzed (40% ER positive, 60% ER untested).
ER level less than 20 fmol/mg on ligand-binding assay deemed ER negative and excluded.
Follow-up for ER-positive group is shorter than for the whole study population.
Modified from (34).