首页> 外文OA文献 >Doxorubicin-paclitaxel: a safe regimen in terms of cardiac toxicity in metastatic breast carcinoma patients. Results from a European Organization for Research and Treatment of Cancer multicenter trial.
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Doxorubicin-paclitaxel: a safe regimen in terms of cardiac toxicity in metastatic breast carcinoma patients. Results from a European Organization for Research and Treatment of Cancer multicenter trial.

机译:阿霉素-紫杉醇:就转移性乳腺癌患者的心脏毒性而言,是一种安全的方案。欧洲癌症研究和治疗组织多中心试验的结果。

摘要

BACKGROUND: The potential cardiotoxicity of the doxorubicin-paclitaxel regimen, when paclitaxel is given shortly after the end of the anthracycline infusion, is an issue of concern, as suggested by small single institution Phase II studies. METHODS: In a large multicenter Phase III trial, 275 anthracycline naive metastatic breast carcinoma patients were randomized to receive either doxorubicin (60 mg/m(2)) followed 30 minutes later by paclitaxel (175 mg/m(2) 3-hour infusion; AT) or a standard doxorubicin-cyclophosphamide regimen (AC; 60/600 mg/m(2)). Both treatments were given once every 3 weeks for a maximum of six cycles. Close cardiac monitoring was implemented in the study design. RESULTS: Congestive heart failure (CHF) occurred in three patients in the AT arm and in one patient in the AC arm (P = 0.62). Decreases in left ventricular ejection fraction to below the limit of normal were documented in 33% AT and 19% AC patients and were not predictive of CHF development. CONCLUSIONS: AT is devoid of excessive cardiac risk among metastatic breast carcinoma patients, when the maximum planned cumulative dose of doxorubicin does not exceed 360 mg/m(2).
机译:背景:如小型单一机构的II期研究所建议的那样,在蒽环类药物输注结束后不久即给予紫杉醇时,阿霉素-紫杉醇方案的潜在心脏毒性是一个令人关注的问题。方法:在一项大型的多中心III期临床试验中,将275名蒽环类初治转移性乳腺癌患者随机接受阿霉素(60 mg / m(2)),然后在30分钟后接受紫杉醇(175 mg / m(2)3小时输注) ; AT)或标准阿霉素-环磷酰胺治疗方案(AC; 60/600 mg / m(2))。两种治疗每3周进行一次,最多六个周期。在研究设计中实施了紧密的心脏监护。结果:充血性心力衰竭(CHF)发生在AT组的3例患者和AC组的1例患者中(P = 0.62)。在33%的AT和19%的AC患者中,左室射血分数降低至正常水平以下,并不能预测CHF的发展。结论:当阿霉素的最大计划累积剂量不超过360 mg / m(2)时,转移性乳腺癌患者中AT不会增加心脏风险。

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