Suppr超能文献

帕妥珠单抗:HER2 阳性乳腺癌患者的新希望。

Pertuzumab: new hope for patients with HER2-positive breast cancer.

机构信息

Department of Medicine, Institute Jules Bordet, L'Université Libre de Bruxelles, Brussels; BrEAST Data Center, Institute Jules Bordet, l'Université Libre de Bruxelles, Brussels.

Department of Medicine, Institute Jules Bordet, L'Université Libre de Bruxelles, Brussels; Breast International Group (BIG), Brussels.

出版信息

Ann Oncol. 2013 Feb;24(2):273-282. doi: 10.1093/annonc/mds328. Epub 2012 Aug 21.

Abstract

BACKGROUND

Human epidermal growth factor receptor 2 (HER2) overexpression is detected in approximately 15% to 20% of all breast cancers (BCs). A revolutionary change in the prognosis of this subgroup of patients has occurred since trastuzumab therapy was introduced into daily clinical practice. However, because trastuzumab resistance is common, new molecules with complementary and/or synergistic mechanisms of action have been developed. Pertuzumab is a new anti-HER2 humanized monoclonal antibody that prevents the formation of HER2 dimers.

MATERIAL AND METHODS

A computer-based literature search was carried out using PubMed (keywords: breast neoplasm, dimerization, HER-2, pertuzumab); data reported at international meetings are included.

RESULTS

This paper describes pertuzumab's mechanism of action, safety, and role in HER2-positive BCs. It also explores the role of pertuzumab as a single agent or combined with trastuzumab by reviewing data from preclinical research to ongoing clinical trials. Recently published trials, particularly the CLEOPATRA study, highlight the efficacy, tolerability, and increase in disease-free survival associated with this novel agent when combined with trastuzumab.

CONCLUSION

The pertuzumab and trastuzumab anti-HER2 dual blockade is likely to represent a substantial advance for patients with HER2-positive BCs and a new milestone on the way to personalized medicine.

摘要

背景

人表皮生长因子受体 2(HER2)过表达约见于 15%至 20%的所有乳腺癌(BC)中。自从曲妥珠单抗治疗引入日常临床实践以来,这一亚组患者的预后发生了革命性的变化。然而,由于曲妥珠单抗耐药很常见,因此已经开发出具有互补和/或协同作用机制的新分子。帕妥珠单抗是一种新型抗 HER2 人源化单克隆抗体,可阻止 HER2 二聚体的形成。

材料和方法

使用 PubMed 进行了基于计算机的文献检索(关键词:乳腺肿瘤,二聚化,HER-2,帕妥珠单抗);包括国际会议上报告的数据。

结果

本文描述了帕妥珠单抗的作用机制、安全性以及在 HER2 阳性 BC 中的作用。通过回顾临床前研究和正在进行的临床试验的数据,探讨了帕妥珠单抗作为单一药物或与曲妥珠单抗联合使用的作用。最近发表的试验,特别是 CLEOPATRA 研究,强调了联合使用该新型药物时与曲妥珠单抗联合使用的疗效、耐受性和无病生存期的增加。

结论

帕妥珠单抗和曲妥珠单抗抗 HER2 双重阻断可能代表了 HER2 阳性 BC 患者的重大进展,也是迈向个体化医学的新里程碑。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验