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静脉注射与口服长春瑞滨联合卡培他滨作为晚期乳腺癌二线治疗:两项连续 II 期研究的回顾性比较。

Intravenous versus oral vinorelbine plus capecitabine as second-line treatment in advanced breast cancer patients. A retrospective comparison of two consecutive phase II studies.

机构信息

Medical Oncology Unit, Vito Fazzi Hospital, Lecce, Italy.

出版信息

Breast. 2010 Jun;19(3):214-8. doi: 10.1016/j.breast.2010.01.015. Epub 2010 Feb 18.

Abstract

Vinorelbine (i.v.) plus capecitabine (oral) combination therapy is active in anthracycline/taxane pretreated patients with metastatic breast cancer. Availability of oral vinorelbine provides this combination in an all-oral formulation. Two consecutive phase II trials differing only in vinorelbine administration routes evaluated their respective activities and tolerabilities in this population. In the i.v. group (n = 38) disease control was 61% (37% PR, 24% SD), median TTP 6.8 months and median survival 11.3 months. In the oral group (n = 38) disease control was 77% (5.4% CR, 34% PR, 38% SD), median TTP 7 months and median survival 10 months. G3-G4 neutropenia was more common in the oral group (p < 0.05); G2-G3 anaemia [5] and G3 thrombocytopenia [1] were observed only in the oral group. Although the comparison between the two regimens was not randomized, the results observed in these two consecutive phase II studies may suggest that oral and iv vinorelbine, in combination with capecitabine, can achieve similar responses in patients with metastatic breast cancer refractory to anthra-taxane combinations.

摘要

长春瑞滨(静脉)联合卡培他滨(口服)治疗方案在蒽环类/紫杉类预处理的转移性乳腺癌患者中具有活性。口服长春瑞滨的可用性使该联合方案成为一种全口服制剂。两项连续的 II 期试验仅在长春瑞滨给药途径上有所不同,评估了该方案在该人群中的各自活性和耐受性。在静脉组(n = 38)中,疾病控制率为 61%(37% PR,24% SD),中位 TTP 为 6.8 个月,中位生存期为 11.3 个月。在口服组(n = 38)中,疾病控制率为 77%(5.4% CR,34% PR,38% SD),中位 TTP 为 7 个月,中位生存期为 10 个月。口服组中更常见 3/4 级中性粒细胞减少症(p < 0.05);仅在口服组中观察到 2/3 级贫血[5]和 3/4 级血小板减少症[1]。尽管这两种方案之间的比较并非随机,但这两项连续的 II 期研究的结果表明,长春瑞滨静脉和口服联合卡培他滨在蒽环类/紫杉类预处理失败的转移性乳腺癌患者中可能产生相似的疗效。

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