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Dose-dense amp; sequential adjuvant cancer chemotherapy

机译:剂量密集和序贯辅助化疗

摘要

Breast cancer is treated by (a) administering to a patient in a first plurality of chemotherapy cycles a therapeutically-effective and well-tolerated amount of doxorubicin in a dose-dense protocol; (b) subsequently administering to the patient in a second plurality of chemotherapy cycles a therapeutically-effective and well-tolerated amount of a taxane chemotherapy agent, for example paclitaxel, in a dose-dense protocol; and (c) subsequently administering to the patient in a third plurality of chemotherapy cycles a therapeutically-effective and well-tolerated amount of cyclophosphainide in a dose-dense protocol. Preferably, the dose dense interval between treatments is about 14 days. The number of cycles in each plurality of chemotherapy cycles is suitably 3 or more, preferably 4. Suitable well-tolerated treatment levels are 60 mg/m2 of doxorubicin, 175 mg/2 of paclitaxel, and 600 mg/2 of cyclophoshamide. A therapeutically effective amount of G-CSF may also be administered during the intervals between treatments in one or more of the chemotherapy cycles.
机译:乳腺癌的治疗方法是:(a)在第一个多个化疗周期中,以剂量密集型方案向患者施用治疗有效且耐受性良好的阿霉素; (b)随后在第二多个化学疗法周期中以剂量密集方案向患者施用治疗有效且耐受良好的紫杉烷化学疗法剂,例如紫杉醇; (c)随后在第三多个化学疗法周期中以剂量密集方案向患者施用治疗有效且耐受良好的量的环磷酰胺。优选地,治疗之间的剂量密集间隔为约14天。每个多个化疗周期中的周期数合适地为3个或更多,优选为4个。合适的耐受良好的治疗水平为60 mg / m 2 阿霉素,175 mg / 2 和600 mg / 2 的环磷酰胺。在一个或多个化学疗法周期的治疗之间的间隔期间,也可以给予治疗有效量的G-CSF。

著录项

  • 公开/公告号US2004229826A1

    专利类型

  • 公开/公告日2004-11-18

    原文格式PDF

  • 申请/专利权人 NORTON LARRY;

    申请/专利号US20030735180

  • 发明设计人 LARRY NORTON;

    申请日2003-12-12

  • 分类号A61K31/704;A61K31/66;A61K31/337;

  • 国家 US

  • 入库时间 2022-08-21 22:25:13

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