Chemotherapy for metastatic breast cancer -: report of a European expert panel

被引:65
作者
Crown, J
Diéras, V
Kaufmann, M
von Minckwitz, G
Kaye, S
Leonard, R
Marty, M
Misset, JL
Osterwalder, B
Piccart, M
机构
[1] Inst Jules Bordet, Chemotherapy Unit, B-1000 Brussels, Belgium
[2] St Vincents Univ Hosp, Dublin, Ireland
[3] Inst Curie, Paris, France
[4] Goethe Univ Frankfurt, Klin Gynakol & Geburtshilfe, D-6000 Frankfurt, Germany
[5] Royal Marsden Hosp, London SW3 6JJ, England
[6] Singleton Hosp, SW Wales Canc Inst, Swansea SA2 8QA, W Glam, Wales
[7] Inst Gustave Roussy, Villejuif, France
[8] Hop Paul Brousse, Villejuif, France
[9] F Hoffmann La Roche Ltd, Basel, Switzerland
关键词
D O I
10.1016/S1470-2045(02)00927-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The anthracyclines doxorubicin and epirubicin, and the taxanes paclitaxel and docetaxel, are effective chemotherapeutic agents for the first-line and second-line treatment of metastatic breast cancer, and their clinical use is widespread. However, for women whose disease has progressed despite receiving these drugs, treatment options are limited. These women often have a good performance status, and may survive for many months or even years, so they should be given the opportunity to benefit from further chemotherapy. The goals of chemotherapy in those patients are to obtain maximum control of symptoms, prevent serious complications, and increase survival without diminishing quality of life. Several agents are used for this purpose, including fluorouracil, docetaxel (in patients who have already received paclitaxel), vinorelbine, and mitomycin c, but because data from controlled trials are limited, a standard regimen has not yet been established. Moreover, these agents may be inconvenient to administer and can be associated with adverse events requiring hospitalisation. Therefore, there is a clear need for additional therapeutic options for patients with metastatic breast cancer. Ideally, agents should have a convenient method of administration, eg, oral, and should be suitable for home-based rather than hospital-based therapy. Treatment should control disease in at least 20-30% of patients with an acceptable side-effect profile. Novel oral therapies have now been developed and are being used increasingly in patients whose disease has progressed following taxane therapy.
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页码:719 / 727
页数:9
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