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多西他赛:标准推荐剂量为100mg/m²,对一些接受过大量化疗的转移性乳腺癌患者有效,但不可行——一项II期单中心研究。

Docetaxel: standard recommended dose of 100 mg/m(2) is effective but not feasible for some metastatic breast cancer patients heavily pretreated with chemotherapy-A phase II single-center study.

作者信息

Salminen E, Bergman M, Huhtala S, Ekholm E

机构信息

Department of Radiotherapy and Oncology, Turku University Hospital, Turku, Finland.

出版信息

J Clin Oncol. 1999 Apr;17(4):1127. doi: 10.1200/JCO.1999.17.4.1127.

Abstract

PURPOSE

Patients with metastatic breast cancer, especially those with progression after several prior chemotherapy treatments, need efficient chemotherapy. This study investigates the efficacy and toxicity of docetaxel in metastatic breast cancer patients with previous chemotherapy for metastatic disease.

PATIENTS AND METHODS

Thirty-one women (median age, 52 years; range, 40 to 65 years) treated for metastatic breast cancer with docetaxel were included. Eleven patients had one metastatic site, 10 patients had two, and 10 patients had three or more. The planned dose of docetaxel per course was the standard treatment of 100 mg/m(2) (or 75 mg/m(2) if liver enzyme levels were abnormal) every 3 weeks, given for six or eight cycles.

RESULTS

The overall response rate was 48% (three complete responses [CR] and 11 partial responses [PR] ), and the median duration of response was 7 months (range, 2 to 16 months). Twenty patients (65%) experienced fatigue, and 27 patients (87%) had alopecia. Fifteen cases (48%) of grade 4 leukopenia were observed. Edema with a weight gain of 2 to 15 kg was seen in 12 patients (39%), and mucositis occurred in 20 patients (65%). Twenty-three patients (74%) interrupted treatment before reaching the planned number of courses, nine patients owing to progression of cancer and 14 owing to toxicity. Dose reduction was required in 18 (61%) of the patients. Only two patients were able to receive the planned eight courses without dose reduction.

CONCLUSION

Docetaxel is highly active in metastatic breast cancer, even as a third-line treatment, and can be considered as an efficient standard option in second-line treatment. The standard recommended dose level of 100 mg/m(2) is not feasible in heavily pretreated patients; therefore, for such patients, an initial dose level not exceeding 75 mg/m(2) is recommended.

摘要

目的

转移性乳腺癌患者,尤其是那些在接受过多次先前化疗后病情进展的患者,需要有效的化疗。本研究调查了多西他赛在先前接受过转移性疾病化疗的转移性乳腺癌患者中的疗效和毒性。

患者与方法

纳入31例接受多西他赛治疗转移性乳腺癌的女性患者(中位年龄52岁;范围40至65岁)。11例患者有一个转移部位,10例患者有两个转移部位,10例患者有三个或更多转移部位。每疗程多西他赛的计划剂量为标准治疗剂量,即每3周100mg/m²(如果肝酶水平异常则为75mg/m²),共给予6或8个周期。

结果

总缓解率为48%(3例完全缓解[CR]和11例部分缓解[PR]),中位缓解持续时间为7个月(范围2至16个月)。20例患者(65%)出现疲劳,27例患者(87%)出现脱发。观察到15例(48%)4级白细胞减少。12例患者(39%)出现体重增加2至15kg的水肿,20例患者(65%)出现粘膜炎。23例患者(74%)在达到计划疗程数之前中断治疗,9例因癌症进展,14例因毒性。18例(61%)患者需要减量。只有2例患者能够在不减量的情况下接受计划的8个疗程。

结论

多西他赛在转移性乳腺癌中具有高活性,即使作为三线治疗,也可被视为二线治疗中的有效标准选择。标准推荐剂量水平100mg/m²在预处理严重的患者中不可行;因此,对于此类患者,建议初始剂量水平不超过75mg/m²。

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