

Author: Dene Simpson Greg L. Plosker
Publisher: Adis International
ISSN: 0012-6667
Source: Drugs, Vol.64, Iss.16, 2004-01, pp. : 1839-1847
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Abstract
Paclitaxel is a antimicrotubule agent with established antitumour activity in a variety of cancers including breast cancer.
The efficacy of intravenous paclitaxel as adjuvant therapy for early breast cancer has been investigated in two large, randomised trials; it was administered sequentially to standard doxorubicin-cyclophosphamide (AC) combination therapy and compared with cycles of AC alone.
In both trials, the addition of sequentially administered paclitaxel to the AC regimen significantly improved disease-free survival at 5 years compared with AC alone. In one of the trials, women who received paclitaxel also had a significant improvement in overall 5-year survival time.
In randomised trials of neoadjuvant therapy for women with early breast cancer, paclitaxel or paclitaxel-containing regimens showed efficacy in terms of response/remission rates, local breast tumour recurrence and proportion of patients eligible for breast-conserving surgery.
The most frequently reported grade 34 adverse events with paclitaxel administered sequentially to AC were haematological events (neutropenia, thrombocytopenia, anaemia) and nausea/vomiting.
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