Abstract | PURPOSE: RESULTS: Patients≥65 years (median: 69) were analyzed. In phase 2 (n=52), overall response rates (ORR) for weekly nab-paclitaxel were 60-64% vs 22% for q3w nab-paclitaxel and 32% for docetaxel. In phase 3 (n=62), ORRs were 27% for q3w nab-paclitaxel and 19% for solvent-based paclitaxel. In phase 2, median progression-free survival (PFS) was 18.9 months for 150 mg/m2 weekly nab-paclitaxel vs 8.5-13.8 months for all other regimens. In phase 3, median PFS for q3w nab-paclitaxel and solvent-based paclitaxel were 5.6 months and 3.5 months, respectively. Weekly nab-paclitaxel resulted in less serious adverse events compared with all other regimens. CONCLUSIONS: Weekly nab-paclitaxel was safe and more efficacious compared with the q3w schedule and with solvent-based taxanes in older patients with MBC.
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Authors | Matti Aapro, Sergei Tjulandin, Paul Bhar, William Gradishar |
Journal | Breast (Edinburgh, Scotland)
(Breast)
Vol. 20
Issue 5
Pg. 468-74
(Oct 2011)
ISSN: 1532-3080 [Electronic] Netherlands |
PMID | 21843943
(Publication Type: Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2011 Elsevier Ltd. All rights reserved. |
Chemical References |
- 130-nm albumin-bound paclitaxel
- Albumins
- Antineoplastic Agents
- Taxoids
- Docetaxel
- Paclitaxel
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Topics |
- Aged
- Aged, 80 and over
- Albumins
(administration & dosage)
- Antineoplastic Agents
(administration & dosage)
- Brain Neoplasms
(drug therapy, mortality, secondary)
- Breast Neoplasms
(drug therapy, mortality, pathology)
- Disease-Free Survival
- Docetaxel
- Drug Administration Schedule
- Female
- Humans
- Liver Neoplasms
(drug therapy, mortality, secondary)
- Lung Neoplasms
(drug therapy, mortality, secondary)
- Neoplasm Metastasis
- Paclitaxel
(administration & dosage)
- Pelvic Neoplasms
(drug therapy, mortality, secondary)
- Taxoids
(administration & dosage)
- Treatment Outcome
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