首页> 外文期刊>Anticancer Research: International Journal of Cancer Research and Treatment >Combination chemotherapy with docetaxel and doxifluridine showed a beneficial outcome in advanced or recurrent breast cancer patients with longer disease-free interval.
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Combination chemotherapy with docetaxel and doxifluridine showed a beneficial outcome in advanced or recurrent breast cancer patients with longer disease-free interval.

机译:多西他赛和多西氟啶联合化疗在无病间隔时间较长的晚期或复发性乳腺癌患者中显示出有益的结果。

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摘要

Fundamental studies have confirmed that combination chemotherapy with docetaxel and doxifluridine (a capecitabine metabolite) is very useful in the treatment of breast cancer. This study investigated the usefulness and tolerability of a combination chemotherapy consisting of docetaxel administration on day 8 of doxifluridine therapy in 40 advanced/recurrent breast cancer patients. The overall response rate was 41.0% in 39 eligible patients. The median time to progression (TTP) for all patients was 295 days. Many responders had lung metastasis, soft tissue metastasis or a good performance status, whereas the clinical response showed no correlations with the estrogen receptor status or prior treatment with an anthracycline. The most common hematological toxicities were leukopenia and neutropenia, but dose reduction or delay of administration of either drug was unnecessary. CONCLUSION: The good response rate and long TTP of this doxifluridine plus docetaxel regimen indicate its potential as a first- or second-line treatment for advanced/recurrent breast cancer patients.
机译:基础研究已经证实,多西他赛和多西氟啶(卡培他滨代谢产物)联合化疗对乳腺癌的治疗非常有用。这项研究调查了由多西他赛组成的联合化疗在多西氟啶治疗第8天的有效性和耐受性,对40例晚期/复发性乳腺癌患者进行了研究。 39名合格患者的总缓解率为41.0%。所有患者的中位进展时间(TTP)为295天。许多反应者有肺转移,软组织转移或良好的工作状态,而临床反应显示与雌激素受体状态或蒽环类以前的治疗无关联。最常见的血液学毒性是白细胞减少症和中性粒细胞减少症,但无需减少剂量或延迟服用任何一种药物。结论:该多西氟啶联合多西他赛方案的良好应答率和长TTP表明其作为晚期/复发性乳腺癌患者的一线或二线治疗的潜力。

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