Trial ID | Design | Patient characteristics and end-points |
---|---|---|
Trials not recruiting or completed | ||
NO17629 | AC × 4 → D100 × 4 versus AC × 4 → D75X × 4 | 1,810 node-positive and high-risk node-negative patients |
NSABP B-38 | ACD × 6 versus AC × 4 (q2w) → P × 4 (q2w) versus AC × 4 (q2w) → PG × 4 (q2w) | 4,800 node-positive patients; DFS (primary); OS, recurrence and distant recurrence-free interval and toxicity (secondary) |
CT/04.22 | FEC × 4 (q2w) → D × 4 (q2w) versus FEC × 4 (q2w) → P × 4 (q2w) | 478 node-positive patients; DFS (primary); OS, recurrence rate, toxicity and QoL (secondary) |
GEICAM 2003-10 | EC × 4 → D × 4 versus ED × 4 → X × 4 | 1,382 node-positive patients; DFS (primary); OS, toxicity, QoL, SNP predictors and molecular markers (secondary) |
GEICAM 2003-02 | FAC × 6 versus FAC × 4 → P × 8w | 1,920 high risk node-negative patients; DFS (primary); OS, toxicity, QoL and prognostic gene profile (2) |
Trials actively recruiting | ||
CALGB-40101 | AC × 4 (q2w) versus AC × 6 (q2w) versus P × 4 (q2w) versus P × 6 (q2w) | 4,646 with 0 to 3 positive nodes patients; DFS (primary); OS, local control, time to distant metastasis, toxicity, amenorrhea, MDR1 haplotype effect, CYP polymorphism effect |
LMU-ADEBAR | EF (d1, d8) C (oral d1–14) × 6 (q4w) versus EC (d1, d21, d42, d63) → D (d84, d105, d126,147) | 446 node-positive patients; time to progression (primary); OS, toxicity and QoL (secondary) |
SWOG-S0221 | AC × 6 (q2w) → P × 6 (q2w) versus AC × 6 (q2w) → P × 12(w) versus AC × 15 (Aw, C oral d1–7) → P × 6 (q2w) versus AC × 15 (Aw, C oral d1–7) → P × 12(w) | 4,500 node-positive and high-risk node-negative patients; DFS (primary); OS, toxicity and prognostic markers (secondary) |
CT/01.04 | D75 × 4 → E90 × 4 versus E75D75 × 6 | 724 high-risk node-negative patients; DF interval (primary); OS and safety (secondary) |
USO 06090 | TAC × 6 versus TC × 6 | HER2 negative and node-positive and high-risk node-negative patients; DFS (primary) |