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长春瑞滨联合顺铂作为二线新辅助化疗方案治疗乳腺癌的疗效

[Effects of vinorelbine plus cisplatin as second-line neoadjuvant chemotherapy regimen in the treatment of breast cancer].

作者信息

Wang Jing, Xu Ling, Ye Jing-ming, Zhao Jian-xin, Duan Xue-ning, Liu Yin-hua

机构信息

Breast Disease Center, First Hospital, Peking University, Beijing 100034, China.

出版信息

Zhonghua Yi Xue Za Zhi. 2013 Jan 8;93(2):93-5.

Abstract

OBJECTIVE

To study the value of a combination of vinorelbine and cisplatin (NP) as second-line neoadjuvant chemotherapy regimen for primary breast cancer.

METHODS

Primary breast cancer patients on neoadjuvant chemotherapy and non-responsive to anthracyclines plus taxanes received the NP regimen. The clinical objective response was evaluated with dynamic contrast-enhanced magnetic resonance imaging (MRI) according to RECIST 1.1 before operation. The pathological response was evaluated by the Miller-Payne grading system. And the toxicities were observed and evaluated according to National Cancer Institute-Common Terminology Criteria Version 3.0 (NCI-CTC v3.0).

RESULTS

A total of 33 breast cancer patients were examined. The outcomes were complete remission (CR, n = 0, 0%), partial remission (PR, n = 16, 48.5%), stable disease (n = 17, 51.5%) and progressive disease (n = 0, 0%). The clinical responsive rate (CR + PR) rate was 48.5%. The pathological response rates were G1 (n = 6, 18.2%), G2 (n = 6, 18.2%), G3 (n = 10, 30.3%), G4 (n = 9, 27.2%) and G5 (n = 2, 6.1%). And the pathological response (G3+G4+G5) was found in 21 cases (63.6%). The most common toxicities included neutropenia and nausea/vomiting. No serious toxicities were observed.

CONCLUSION

As a well-tolerated and effective regimen, NP regimen may be recommended as an option of second-line neoadjuvant chemotherapy regimen for primary breast cancer.

摘要

目的

研究长春瑞滨联合顺铂(NP)方案作为原发性乳腺癌二线新辅助化疗方案的价值。

方法

对新辅助化疗且对蒽环类药物加紫杉类药物无反应的原发性乳腺癌患者采用NP方案。术前根据RECIST 1.1,采用动态对比增强磁共振成像(MRI)评估临床客观反应。通过Miller-Payne分级系统评估病理反应。并根据美国国立癌症研究所通用术语标准第3.0版(NCI-CTC v3.0)观察和评估毒性。

结果

共检查33例乳腺癌患者。结果为完全缓解(CR,n = 0,0%)、部分缓解(PR,n = 16,48.5%)、疾病稳定(n = 17,51.5%)和疾病进展(n = 0,0%)。临床缓解率(CR + PR)为48.5%。病理反应率为G1(n = 6,18.2%)、G2(n = 6,18.2%)、G3(n = 10,30.3%)、G4(n = 9,27.2%)和G5(n = 2,6.1%)。21例(63.6%)出现病理反应(G3+G4+G5)。最常见的毒性包括中性粒细胞减少和恶心/呕吐。未观察到严重毒性。

结论

作为一种耐受性良好且有效的方案,NP方案可推荐作为原发性乳腺癌二线新辅助化疗方案的选择。

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