首页> 外文期刊>International Journal of Clinical Pharmacology Research >Paclitaxel-ifosfamide for anthracycline-resistant advanced breast cancer.
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Paclitaxel-ifosfamide for anthracycline-resistant advanced breast cancer.

机译:紫杉醇-异环磷酰胺用于抗蒽环类的晚期乳腺癌。

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Thirty-one patients with advanced breast cancer either resistant to anthracycline-based regimens or relapsing after anthracycline-based adjuvant chemotherapy received a combination of a 3-h infusion of paclitaxel 135 mg/m2 on day 1 and a 4-h infusion of ifosfamide 1.7 g/m2 on days 2 to 4 of a 22-day cycle. For inclusion in the study, patients had to have measurable or evaluable progressive metastasis or local disease, and to have received only one prior regimen for metastatic disease; 31 patients with a median age of 49 years (range: 30-69) entered the study. Nine patients (29%) had lung metastasis, while 17 (55%) had liver metastasis, and 19 (61%) had bone metastasis. Only seven patients (23%) had lymph node metastasis and four (13%) had skin metastasis. A median of seven cycles of treatment was delivered. Responses were evaluated according to World Health Organization (WHO) guidelines and side effects according to National Cancer Institute (NCI) criteria. A panel of oncologists and one radiologist reviewed all responses. At baseline, only three patients (10%) were free from the adverse effects of the prior therapy; severe nonhematological toxicity occurred in less than 8% of patients. However neutropenia grade 3-4 occurred in 88%, while only 3% had severe infections. Severe thrombocytopenia and anemia were rare (4% and 8%, respectively). The overall response rate was 42% (13% complete response). Median survival and progression-free survival rates after initiation of treatment were 19.3 months and 6.1 months, respectively. With an objective response rate of 42% and median survival of 19 months, the combination of paclitaxel and ifosfamide seems to offer a promising regimen with acceptable side effects in advanced breast cancer patients relapsing after anthracycline-based adjuvant treatment or resistant to anthracycline treatment.
机译:31名晚期乳腺癌患者对基于蒽环类药物的治疗方案耐药或在基于蒽环类药物的辅助化疗后复发,在第1天接受了3小时的紫杉醇135 mg / m2输注和4小时的异环磷酰胺1.7输注的组合22天周期的第2至4天以g / m2为单位。为了纳入研究,患者必须具有可测量或可评估的进行性转移或局部疾病,并且仅接受过一种转移性疾病的治疗方案。 31名中位年龄为49岁(范围:30-69)的患者进入了研究。 9例(29%)发生了肺转移,而17例(55%)发生了肝转移,19例(61%)发生了骨转移。只有7例(23%)有淋巴结转移,而4例(13%)有皮肤转移。进行了七个周期的中位治疗。根据世界卫生组织(WHO)指南评估反应,并根据美国国家癌症研究所(NCI)标准评估副作用。一组肿瘤科医生和一名放射科医生审查了所有反应。在基线时,只有三名患者(10%)没有先前治疗的不良反应。不到8%的患者发生了严重的非血液学毒性。但是88%的患者发生3-4级中性粒细胞减少,而只有3%的患者患有严重感染。严重的血小板减少症和贫血很少见(分别为4%和8%)。总体回应率为42%(完全回应为13%)。开始治疗后的中位生存期和无进展生存期分别为19.3个月和6.1个月。紫杉醇联合异环磷酰胺的客观缓解率为42%,中位生存期为19个月,在以蒽环类为基础的辅助治疗后复发或对蒽环类药物耐药的晚期乳腺癌患者中,似乎提供了一种有希望的方案,具有可接受的副作用。

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