Docetaxel compared with sequential methotrexate and 5-fluorouracil in patients with advanced breast cancer after anthracycline failure:: a randomised phase III study with crossover on progression by the Scandinavian Breast Group

被引:222
作者
Sjöström, J
Blomqvist, C
Mouridsen, H
Pluzanska, A
Ottosson-Lönn, S
Bengtsson, NO
Ostenstad, B
Mjaaland, I
Palm-Sjövall, M
Wist, E
Valvere, V
Anderson, H
Bergh, J
机构
[1] Univ Helsinki, Cent Hosp, Dept Oncol, FIN-00290 Helsinki, Finland
[2] Copenhagen Univ Hosp, Rigshosp, Copenhagen, Denmark
[3] Med Univ Lodz, Dept Oncol, Lodz, Poland
[4] Sahlgrens Univ Hosp, Gothenburg, Sweden
[5] Univ Umea Hosp, S-90185 Umea, Sweden
[6] Univ Lund Hosp, S-22185 Lund, Sweden
[7] Univ Uppsala Hosp, Uppsala, Sweden
[8] Ulleval Hosp, Oslo, Norway
[9] Cent Hosp Rogaland, Stavanger, Norway
[10] Univ Tromso Hosp, N-9012 Tromso, Norway
[11] Estonian Canc Ctr, Tallinn, Estonia
关键词
breast cancer; chemotherapy; docetaxel; anthracycline failure; methotrexate; 5-fluorouracil;
D O I
10.1016/S0959-8049(99)00122-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The aim of this study was to compare the efficacy and tolerability of docetaxel to methotrexate and 5-fluorouracil in advanced breast cancer after anthracycline failure. A randomised multicentre trial was conducted in 283 patients with advanced breast cancer who had failed previous anthracycline treatment. Docetaxel at a dose of 100 mg/m(2) every 3 weeks (n=143) was compared with sequential methotrexate and 5-fluorouracil (MF; n = 139) given at day 1 and 8 every 3 weeks at dosages of 200 mg/ m(2) and 600 mg/m(2), respectively. After progression, crossover to the alternative treatment group was recommended. There was a significantly higher overall response rate in the docetaxel 42% (CR 8% + PR 34%) than in the MF arm 21% (CR 3% + PR 18%) (P< 0.001). The median time to progression (TTP) was 6.3 months in the docetaxel arm and 3.0 months in the RIF arm (P<0.001). Docetaxel also had a significantly higher response rate of 27% following crossover compared with MF (12%). Significantly more side-effects (leucopenia, infections, neuropathy, oedema, asthenia, skin, nail changes, alopecia) were seen in the docetaxel than in the MF group. However, grade 3 and 4 side-effects were infrequent with both drugs, with the exception of fatigue, alopecia and infections. Median overall survival (OS) including crossover phase was 10.4 months in the docetaxel and 11.1 months in the MF arm (P= 0.79). Based on the response rate and the primary endpoint of TTP, docetaxel is superior to sequential methotrexate and 5-fluorouracil in advanced breast cancer after anthracycline failure. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
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页码:1194 / 1201
页数:8
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