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Combined doxorubicin and paclitaxel in advanced breast cancer: Effective and cardiotoxic
Author(s): Gehl J, Boesgaard M, Paaske T, Jensen BV, Dombernowsky P
Source: ANNALS OF ONCOLOGY    Volume: 7    Issue: 7    Pages: 687-693    Published: SEP 1996  
Times Cited: 155     References: 29     
Abstract: Background: Paclitaxel has shown activity in metastatic breast cancer, including anthracycline-resistant breast cancer. The efficacy, toxicity and optimal scheduling of the combination of the two drugs needs to be defined.

Patients and methods: Thirty women with advanced breast cancer who had undergone at most one prior adjuvant chemotherapy regimen, were treated at three different dose levels with doxorubicin (50, 60 and 60 mg/m(2)) followed 30 minutes later by paclitaxel (155, 175 and 200 mg/m(2), respectively) every 3 weeks.

Results: The overall response rate was 83% (95% CI: 64-94), with 24% of patients achieving CR. The median response duration for complete responders was 11 months (range 4-14+) and median survival 18 months (range 3-28+). Two hundred sixty-five treatment courses were given (median 9, range 3-13) and the median cumulative dose of doxorubicin was 369 mg/m(2) (range 114-550). The main toxicities were neutropenia, parestesia, nausea/vomiting, alopecia, myalgia and cardiotoxicity. Fifteen patients (50%) had reductions of left ventricular ejection fraction to below normal levels and 6 of these patients (20%) developed congestive heart failure.

Conclusion: The combination of doxorubicin and paclitaxel is highly active, but is accompanied by the dose-limiting toxic effects of neutropenia, neuropathy and cardiotoxicity.

Document Type: Article
Language: English
Reprint Address: Gehl, J (reprint author), HERLEV UNIV HOSP, DEPT ONCOL, 75 HERLEV RINGVEJ, DK-2730 HERLEV, DENMARK
Addresses:
1. NATL UNIV HOSP, DEPT ONCOL, COPENHAGEN, DENMARK
2. HERLEV UNIV HOSP, DEPT CLIN PHYSIOL & NUCL MED, DK-2730 HERLEV, DENMARK
Publisher: KLUWER ACADEMIC PUBL, SPUIBOULEVARD 50, PO BOX 17, 3300 AA DORDRECHT, NETHERLANDS
Subject Category: Oncology
IDS Number: VL799
ISSN: 0923-7534
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