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曲妥珠单抗在HER-2阳性乳腺癌患者新辅助治疗中的应用研究进展
引用本文:刘君,杨艳芳,顾林.曲妥珠单抗在HER-2阳性乳腺癌患者新辅助治疗中的应用研究进展[J].中国肿瘤临床,2014,41(16):1065-1068.
作者姓名:刘君  杨艳芳  顾林
作者单位:天津医科大学肿瘤医院乳腺二科,国家肿瘤临床医学研究中心,乳腺癌防治教育部重点实验室,天津市肿瘤防治重点实验室(天津市300060)
摘    要:曲妥珠单抗是人表皮生长因子受体-2(human epidermal growth factor receptor-2,HER-2)的特异性抑制剂,在HER-2阳性乳腺癌患者新辅助治疗中的应用日益广泛。大规模的随机、对照临床试验证实,新辅助化疗联合曲妥珠单抗与单纯化疗比较能显著提高病理完全缓解(pathologic complete response,pCR)率。在曲妥珠单抗联合化疗的基础上加用拉帕替尼较单用曲妥珠单抗可大大提高pCR率。蒽环与非蒽环类化疗药物均可作为曲妥珠单抗的联合用药,内分泌治疗也可作为雌激素受体阳性患者的联合用药。pCR是曲妥珠单抗新辅助治疗后生存获益的独立预后因素,HER-2转阴而未达到pCR的患者为不良预后因素。本文将对曲妥珠单抗在HER-2阳性乳腺癌患者新辅助治疗中的研究进展进行综述。 

关 键 词:曲妥珠单抗    新辅助治疗    人表皮生长因子受体-2    乳腺癌
收稿时间:2013-12-27

Advanced research on neoadjuvant therapy with trastuzumab in HER2-positive breast cancer
Institution:The Second Department of Breast Cancer, Tianjin Medical University Cancer Institute and Hospital; National Clinical Research Center for Cancer; Key Laboratory of Breast Cancer Prevention and Therapy, Ministry of Education; Key Laboratory of Cancer Prevention and Therapy Tianjin, Tianjin 300060, China
Abstract:Trastuzumab is a specific inhibitor against human epidermal growth factor receptor-2 (HER-2). Trastuzumab is widely used in the neo-adjuvant treatment of HER-2 breast cancer. Large-scale randomized and controlled clinical trials have demonstrated that pathologic complete response rates (pCRs) were significantly increased with neo-adjuvant trastuzumab therapy plus chemotherapy than with regular chemotherapy. The use of trastuzumab plus chemotherapy with lapatinib supplements could further improve pCR rates. Anthracycline and non-anthracycline drugs could both be used concurrently with trastuzumab. Endocrine therapy could be used as an alternative for estrogen receptor-positive patients. pCR is a powerful predictor of long-term outcomes in HER-2 positive patients under neo-adjuvant therapy with trastuzumab. However, patient loss of HER-2 expression with residual disease after neo-adjuvant therapy with trastuzumab is a poor prognostic factor. This study paper will provide a review of related research. 
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