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首页> 外文期刊>Clinical breast cancer >A phase II study of lipoplatin (liposomal cisplatin)/vinorelbine combination in HER-2eu-negative metastatic breast cancer.
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A phase II study of lipoplatin (liposomal cisplatin)/vinorelbine combination in HER-2eu-negative metastatic breast cancer.

机译:脂质铂(顺铂脂质体)/长春瑞滨联合治疗HER-2 /中性阴性转移性乳腺癌的II期研究。

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摘要

We assessed the efficacy and safety of a liposomal cisplatin (lipoplatin) and vinorelbine combination in metastatic breast cancer (MBC). Thirty-five patients were treated. The objective response rate was 53.1% and the median survival time was 22 months. Grade 3/4 neutropenia was observed in 44% of cycles, and febrile neutropenia was seen in 4 patients (11.4%). No grade 3/4 nephrotoxicity or neuropathy was noted. This combination is effective and well tolerated in patients with MBC and it warrants investigation as first-line treatment. BACKGROUND: Liposomal cisplatin (lipoplatin) has a mechanism of action similar to that of cisplatin, with reduced toxicities and enhanced or similar efficacy. We wanted to assess the efficacy and safety of a lipoplatin/vinorelbine combination in a phase II clinical trial in metastatic breast cancer (MBC). METHODS: Thirty-five patients with HER-2eu-negative (HER-2eu(-)) MBC were enrolled. Lipoplatin 120 mg/m(2) (days 1, 8, and 15) and vinorelbine 30 mg/m(2) (days 1 and 8) were administered in a 21-day cycle. RESULTS: Thirty-five patients were included in the intent-to-treat (ITT) analysis; 32 patients were evaluable for response. The objective response rate was 53.1%. Complete response (CR) was achieved in 3 patients (9.4%), partial response (PR) was seen in 14 patients (43.8%), stable disease (SD) was obtained in 12 patients (37.5%), and progressive disease (PD) was seen in 3 patients (9.4%). Median time to disease progression was 8 months (range 6-10 months). After a median follow-up of 15.5 months, 18 patients were still alive; the median survival time was 22 months (95% confidence interval [CI], 14-30). A total of 174 cycles were administered. Neutropenia was the most frequent hematologic toxicity, with grade 3/4 neutropenia observed in 44% of cycles. Febrile neutropenia was observed in 4 patients (11.4%). No grade 3/4 nephrotoxicity or neuropathy was noted. Grade 1/2 nephrotoxicity occurred in 8 patients (22.9%) and grade 3 vomiting was seen in 3 patients (8.6%). CONCLUSIONS: The results of this trial reveal that vinorelbine/lipoplatin is effective in treating patients with MBC. This regimen is well tolerated with no grade 3/4 nephrotoxicity or neuropathy. The investigation of this regimen as first-line treatment in MBC is warranted.
机译:我们评估了脂质体顺铂(lipoplatin)和长春瑞滨组合在转移性乳腺癌(MBC)中的疗效和安全性。治疗了35例患者。客观缓解率为53.1%,中位生存时间为22个月。在44%的周期中观察到3/4级中性粒细胞减少,在4例患者中观察到发热性中性粒细胞减少(11.4%)。没有发现3/4级肾毒性或神经病。这种组合对MBC患者有效且耐受性良好,值得一线治疗。背景:脂质体顺铂(lipoplatin)的作用机理与顺铂相似,但毒性降低,疗效增强或相似。我们想在转移性乳腺癌(MBC)的II期临床试验中评估脂铂/长春瑞滨组合的疗效和安全性。方法:35例HER-2 / neu阴性(HER-2 / neu(-))MBC患者入组。以21天的周期服用120 mg / m(2)的Lipoplatin(第1、8和15天)和长春瑞滨30 mg / m(2)(第1和8天)。结果:35例患者被纳入意向治疗(ITT)分析; 32位患者的反应可评估。客观回应率为53.1%。 3例患者(9.4%)达到完全缓解(CR),14例患者(43.8%)达到部分缓解(PR),12例患者(37.5%)获得稳定疾病(SD),而进行性疾病(PD) )出现在3例患者中(9.4%)。疾病进展的中位时间为8个月(范围6-10个月)。中位随访15.5个月后,仍有18例患者还活着。中位生存时间为22个月(95%置信区间[CI]为14-30)。总共进行了174个循环。中性粒细胞减少是最常见的血液学毒性,在44%的周期中观察到3/4级中性粒细胞减少。在4例患者中观察到发热性中性粒细胞减少(11.4%)。没有发现3/4级肾毒性或神经病。 8名患者发生1/2级肾毒性(22.9%),3名患者发生3级呕吐(8.6%)。结论:该试验的结果表明长春瑞滨/脂铂可有效治疗MBC患者。该方案耐受良好,无3/4级肾毒性或神经病变。有必要对作为MBC一线治疗方案的这种方案进行研究。

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