Taxoids in combination chemotherapy for metastatic breast cancer

被引:18
作者
Dieras, V
Fumoleau, P
Bourgeois, H
Misset, JL
Azli, N
Pouillart, P
机构
[1] HOP PAUL BROUSSE, VILLEJUIF, FRANCE
[2] CTR RENE GAUDUCHEAU, ST HERBLAIN, FRANCE
[3] RHONE POULENC RORER, ANTONY, FRANCE
关键词
metastatic breast cancer; drug combinations; docetaxel (Taxotere(R)); paclitaxel (Taxol(R)); anthracyclines; vinorelbine (Navelbine(R));
D O I
10.1097/00001813-199608002-00012
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The rationale for the development of new drug combinations is to combine optimal doses of drugs with single agent activity which are not cross-resistant and have nonoverlapping toxicities. Anthracyclines are widely accepted as the agents of choice for first-line treatment of metastatic breast cancer and have been tested in combination with the taxoids, docetaxel (Taxotere(R)) and paclitaxel (Taxol(R)). Toxicity problems have emerged using anthracyclines and paclitaxel, with sequence- and schedule-dependent toxic effects including dose-limiting typhlitis and mucositis, as well as febrile neutropenia and, in one study, cardiomyopathy. The dose-limiting toxicities of the combination of docetaxel and doxorubicin are neutropenia and infection, and preliminary results indicate a response rate of 89%. There is a need to develop a combination treatment regimen which is non-cross-resistant with anthracyclines. Vinorelbine (Navelbine(R)) has single agent activity against metastatic breast cancer and has been used in combination with taxoids.;The dose-limiting toxicities of the vinorelbine-paclitaxel combination are febrile neutropenia, pelvic pain, fatigue and paraesthesias. The dose-limiting toxicities of the combination of docetaxel end vinorelbine are febrile neutropenia and mucositis. The overall response rate for this combination was 67% and studies are ongoing.
引用
收藏
页码:47 / 52
页数:6
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