首页> 外文期刊>Clinical oncology >Vinorelbine and Infusional 5-fluorouracil in Anthracycline and Taxane Pre-treated Metastatic Breast Cancer.
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Vinorelbine and Infusional 5-fluorouracil in Anthracycline and Taxane Pre-treated Metastatic Breast Cancer.

机译:长春瑞滨和5-氟尿嘧啶输注蒽环类和紫杉烷类药物可治疗转移性乳腺癌。

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AIMS: To evaluate the efficacy and toxicity of a combination of intravenous vinorelbine and 5-fluorouracil (5-FU) given by continuous infusion in the treatment of metastatic breast cancer previously treated with anthracyclines and taxanes. MATERIALS AND METHODS: Sixty-one patients with metastatic breast cancer were treated with intravenous vinorelbine 30mg/m(2) on days 1 and 8 of each 21-day cycle together with 5-FU 200mg/m(2)/day by continuous infusion. All had previously been treated with an anthracycline and 41% had also been previously treated with a taxane. All had normal haematological, renal and hepatic function and all but three had an Eastern Cooperative Oncology Group performance score of 2 or better. RESULTS: The overall response rate by World Health Organization criteria was 46% (28 patients); excluding nine non-evaluable patients gave a response rate of 54%. In patients who had previously been treated with both an anthracycline and a taxane, a response rate of 50% was observed (12 of 24 patients). Severe toxicity was uncommon, as was toxicity attributable to infusional 5-FU. Myelosuppression was rarely severe, but was common and led to delay or dose reduction in 38% of treatments. Eleven patients (18%) were admitted with fever and/or neutropenia and one patient died. The median received dose intensity was vinorelbine 16mg/m(2)/week and 5-FU 143mg/m(2)/day. CONCLUSIONS: The combination of vinorelbine and infusional 5-FU is active in metastatic breast cancer, including in patients previously treated with an anthracycline and a taxane. Toxicity is generally manageable, but myelosuppression is significant at this dose regimen. Recommended doses for routine clinical use are 5-FU 200mg/m(2)/day and intravenous vinorelbine 30mg/m(2) days 1 and 15 on a 28-day cycle.
机译:目的:评估静脉输注长春瑞滨和5-氟尿嘧啶(5-FU)连续输注联合治疗先前用蒽环类和紫杉烷类治疗的转移性乳腺癌的疗效和毒性。材料与方法:在每个21天周期的第1天和第8天,对静脉转移性长春瑞滨30mg / m(2)和5-FU 200mg / m(2)/天的静脉输注长春瑞滨30例,共61例转移性乳腺癌患者。所有患者先前都曾用蒽环类药物治疗过,另有41%的患者先前也曾用紫杉烷治疗过。所有人的血液,肾和肝功能均正常,除三人以外,所有人的东部合作肿瘤小组的表现得分均在2分或更高。结果:按照世界卫生组织的标准,总缓解率为46%(28例患者)。排除9名无法评估的患者,其缓解率为54%。在先前接受蒽环类和紫杉烷类药物治疗的患者中,观察到的缓解率为50%(24名患者中的12名)。严重毒性不常见,而输注5-FU引起的毒性也不常见。骨髓抑制很少是严重的,但很普遍,导致38%的治疗延迟或减少剂量。十一名患者(占18%)因发烧和/或中性粒细胞减少症而入院,一名患者死亡。中位接受剂量强度是长春瑞滨16mg / m(2)/周和5-FU 143mg / m(2)/天。结论:长春瑞滨和5-FU输注的组合在转移性乳腺癌中具有活性,包括先前用蒽环类和紫杉烷类药物治疗的患者。毒性通常是可以控制的,但是在这种剂量方案下,骨髓抑制作用是显着的。常规临床使用的建议剂量为5-FU 200mg / m(2)/天,静脉长春瑞滨30mg / m(2)在第28天的第1天和第15天。

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