Trial | Treatments | Patients | Method |
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GeparQuattro, 2010 | (n=-9) vs. (n=-9) | Patients with large operable or locally advanced tumors, with hormone receptor-negative tumors, or with receptor-positive tumors but also clinically node-positive disease | Sample size: -9/-9 Primary endpoint: FU duration: |
Mavroudis, 2010 | docetaxel 75 mg/m(2) on day 1 plus capecitabine 950 mg/m(2) orally twice daily on days 1-14 (DC) in 21-day cycles (n=-9) vs. docetaxel 75 mg/m(2) plus epirubicin 75 mg/m(2) (DE) on day 1 (n=-9) | women with advanced breast cancer | Sample size: -9/-9 Primary endpoint: FU duration: |
Lee, 2008 | (n=-9) vs. (n=-9) | women with axillary node positive, stage II/III breast cancer | Sample size: -9/-9 Primary endpoint: FU duration: |
Verma, 2005 | 21-day cycles of oral capecitabine 1250 mg/m2 twice daily, on Days 1-14, plus docetaxel 75 mg/m2 Day 1 (n=255) vs. docetaxel 100 mg/m2 on Day 1 (n=256) | patients with anthracycline-pretreated metastatic breast carcinoma | Sample size: 255/256 Primary endpoint: FU duration: |
Miles, 2004 | (n=511) vs. (n=0) | patients with anthracycline-pretreated advanced/metastatic breast cancer | Sample size: 511/0 Primary endpoint: FU duration: |
O'Shaughnessy, 2002 | 21-day cycles of oral capecitabine 1,250 mg/m(2) twice daily on days 1 to 14 plus docetaxel 75 mg/m(2) on day 1 (n=255) vs. docetaxel 100 mg/m(2) on day 1 (n=256) | patients with advanced breast cancer | Sample size: 255/256 Primary endpoint: FU duration: |
Talbot, 2002 | intermittent oral capecitabine (1255 mg m(-2) twice daily, days 1-14, (22 patients)) (n=-9) vs. i.v. paclitaxel (175 mg m(-2), (n=-9) | patients with metastatic/advanced breast cancer pretreated with anthracyclines | Sample size: -9/-9 Primary endpoint: FU duration: |
Moiseenko, 2000 | (n=-9) vs. (n=-9) | | Sample size: -9/-9 Primary endpoint: FU duration: |