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米托蒽醌、环磷酰胺和5-氟尿嘧啶治疗激素难治性转移性乳腺癌

Mitoxantrone, cyclophosphamide, and 5-fluorouracil in the treatment of hormonally unresponsive metastatic breast cancer.

作者信息

Holmes F A, Yap H Y, Esparza L, Buzdar A U, Hortobagyi G N, Blumenschein G R

出版信息

Semin Oncol. 1984 Sep;11(3 Suppl 1):28-31.

PMID:6385262
Abstract

Fifty-five patients with newly diagnosed, estrogen receptor negative, metastatic breast cancer were entered in a trial of mitoxantrone, 10 mg/m2 intravenous (IV), cyclophosphamide, 500 mg/m2 IV, and 5-fluorouracil, 1000 mg/m2 IV, which were given on day 1 of a 21-day treatment interval. This trial was designed to test the efficacy of substituting mitoxantrone for doxorubicin as part of a combination that has proved to be effective in inducing remission. The trial was also intended to evaluate the response of resistant disease and of stable metastatic disease to a combination of doxorubicin and vinblastine sulfate. The cardiotoxic potential of mitoxantrone was evaluated in all the patients by serial measurements of ejection fraction and by endocardial biopsy of the right ventricle. Patients who achieved a complete response or a partial response (with bone as the only site of disease) on the three-drug combination were continued on this treatment for 2 years, or for 1 year following a complete response, whichever was shorter or as cardiac monitoring permitted. Therapy with doxorubicin, 25 mg/m2/d for two days, followed by continuous infusion vinblastine sulfate, 1.4 mg/m2/d for four days, was given to all patients who progressed after two courses or were stable after six courses of three-drug therapy. The preliminary results from 50 patients show that 4 attained a complete response and 30 a partial response, giving a total response rate of 68%. The median duration of response was more than 7 months (range greater than 5 to greater than 15 months). One patient in complete remission relapsed after 8 months and failed reinduction therapy with doxorubicin-vinblastine sulfate. Myelosuppression, principally granulocytopenia, was the major side effect of cyclophosphamide-mitoxantrone-5-fluorouracil. Mild to moderate vomiting occurred in 76% of patients and alopecia in 88%. This therapy was discontinued in four patients because of a decreased cardiac ejection fraction and/or symptoms of heart failure. No cardiac biopsy score, however, has been greater than 1.0. These results suggest that a combination of cyclophosphamide-mitoxantrone-5-fluorouracil is effective in untreated, estrogen receptor negative, metastatic breast cancer and is comparable to the doxorubicin combination. Myocardial injury occurs with mitoxantrone, and a safe cumulative dose has yet to be established.

摘要

55例新诊断的雌激素受体阴性转移性乳腺癌患者参加了一项关于米托蒽醌、环磷酰胺和5-氟尿嘧啶的试验。米托蒽醌剂量为10mg/m²静脉注射(IV),环磷酰胺剂量为500mg/m²静脉注射,5-氟尿嘧啶剂量为1000mg/m²静脉注射,于21天治疗间隔的第1天给药。该试验旨在测试用米托蒽醌替代多柔比星作为联合用药一部分的疗效,这种联合用药已被证明在诱导缓解方面有效。该试验还旨在评估耐药性疾病和稳定转移性疾病对多柔比星和硫酸长春碱联合用药的反应。通过连续测量射血分数和右心室心内膜活检对所有患者评估米托蒽醌的心脏毒性潜力。在三联药物联合治疗中达到完全缓解或部分缓解(仅骨为疾病部位)的患者继续接受该治疗2年,或在完全缓解后接受1年治疗,以较短时间或心脏监测允许的时间为准。对于在两个疗程后病情进展或在六个疗程的三联药物治疗后病情稳定的所有患者,给予多柔比星25mg/m²/d静脉注射2天,随后硫酸长春碱1.4mg/m²/d持续静脉输注4天的治疗。50例患者的初步结果显示,4例达到完全缓解,30例达到部分缓解,总缓解率为68%。缓解的中位持续时间超过7个月(范围大于5至大于15个月)。1例完全缓解的患者在8个月后复发,用多柔比星-硫酸长春碱再诱导治疗失败。骨髓抑制,主要是粒细胞减少,是环磷酰胺-米托蒽醌-5-氟尿嘧啶的主要副作用。76%的患者出现轻至中度呕吐,88%的患者出现脱发。4例患者因射血分数降低和/或心力衰竭症状而停止该治疗。然而,心脏活检评分均未超过1.0。这些结果表明,环磷酰胺-米托蒽醌-5-氟尿嘧啶联合用药对未经治疗的雌激素受体阴性转移性乳腺癌有效,且与多柔比星联合用药相当。米托蒽醌会导致心肌损伤,安全累积剂量尚未确定。

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