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Docetaxel and cisplatin combination chemotherapy in metastatic breast cancer patients with previous exposure to anthracyclines.

机译:多西紫杉醇和顺铂联合化疗用于先前接触蒽环类药物的转移性乳腺癌患者。

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摘要

We evaluated the efficacy and safety of the combination of docetaxel and cisplatin in metastatic breast cancer (MBC) patients previously treated with anthracycline-containing regimens. Between June 1999 and December 2002, 50 female MBC patients (median age 43 years; range 29-64) received docetaxel 75 mg/m(2) and cisplatin 75 mg/m(2) on day 1 of each 4-week cycle. A total of 226 cycles (median four cycles per patient) were administered as first-line (23 patients) or second-line (27 patients) treatment. Five patients (10%) achieved a complete response (CR) and 15 (30%) had partial responses (PR), giving an overall response rate of 40% (95% CI, 26.4 approximately 53.6%). The median duration of response was 6.1 months (range, 2.3 approximately 29.2(+) months). With a median follow-up of 15.9 months, median time to progression was 6.2 months (range 1 approximately 22.5(+) months). Toxicities included grades III and IV neutropenia in nine (18%) and ten (20%) patients, respectively, and febrile neutropenia in seven patients (14%). In conclusion, our data show that docetaxel plus cisplatin is effective with the manageable toxicity profile in MBC patients previously treated with anthracyclines.
机译:我们评估了多西他赛和顺铂联合使用在先前接受含蒽环类药物治疗的转移性乳腺癌(MBC)患者中的疗效和安全性。在1999年6月至2002年12月之间,每4周周期的第1天,有50名女性MBC患者(中位年龄43岁;范围29-64)接受多西他赛75 mg / m(2)和顺铂75 mg / m(2)。一线(23例)或二线(27例)治疗总共进行了226个周期(每位患者中位数四个周期)。五名患者(10%)获得了完全缓解(CR),而十五名患者(30%)获得了部分缓解(PR),总体缓解率为40%(95%CI,26.4约53.6%)。中位反应持续时间为6.1个月(范围为2.3约29.2(+)个月)。中位随访时间为15.9个月,中位进展时间为6.2个月(范围1约为22.5(+)个月)。毒性分别为9名(18%)和10名(20%)患者的III级和IV级中性粒细胞减少,以及7名患者(14%)的发热性中性粒细胞减少。总之,我们的数据表明,多西他赛加顺铂在先前接受蒽环类药物治疗的MBC患者中具有可控的毒性谱,有效。

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