Weekly docetaxel in patients with pretreated metastatic breast cancer:: a phase II trial

被引:14
作者
Mey, U
Gorschlüt er, M
Ziske, C
Kleinschmidt, R
Glasmacher, A
Schmidt-Wolf, IGH
机构
[1] Univ Bonn, Med Klin & Poliklin 1, D-53105 Bonn, Germany
[2] Markus Krankenhauses, Med Klin 1, Frankfurt, Germany
关键词
breast cancer; docetaxel; weekly regimen;
D O I
10.1097/00001813-200303000-00007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Docetaxel has consistently demonstrated its high activity as an antineoplastic agent in the treatment of metastatic breast cancer. However, 90% of patients receiving the recommended dose of 100 mg/m(2) every 3 weeks will develop grade 3 or 4 neutropenia. Recent data suggest that the safety profile of a weekly docetaxel regimen compared favorably with the standard 3-week schedule. Thus, we initiated a phase II study to assess the efficacy and toxicity of weekly docetaxel in pretreated patients with metastatic breast cancer. Twenty patients with advanced, anthracycline-refractory breast cancer were included in this phase 11 trial. Docetaxel was administered at a starting dose of 40 mg/m(2), repeated once a week for 3 consecutive weeks followed by a 1-week rest period (1 cycle). Patients were evaluated for tumor response every 8 weeks (after every other cycle). Therapy was continued for a maximum of six courses in patients showing tumor response or stable disease. Twenty patients received a total of 204 weekly infusions of docetaxel. The mean number of treatments was 10.2 (range 1-18). Eighteen patients were assessable for response. Five patients achieved a partial response and six patients showed either stable disease or a minor response. Seven patients had disease progression. The median survival was 7.8 months. Grade 3/4 leukopenia occurred in two patients. No other grade 3 or 4 hematologic toxicities were observed. The following grade 3/4 nonhematologic toxicities were seen: nausea/vomiting (one patient), infection (one patient), mucositis (two patients) and diarrhea (one patient). Three patients withdrew from the study due to dose-limiting toxicities (one due to severe neutropenia and two due to mucositis). We conclude that administration of docetaxel at a dose of 40 mg/m(2) was effective and well tolerated even in heavily pretreated patients with metastatic breast cancer. This regimen is associated with only mild myelosuppression.
引用
收藏
页码:233 / 238
页数:6
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