Wong Andrea L A, Lee Soo-Chin
Department of Haematology-Oncology, National University Cancer Institute, National University Health System, Singapore 119228.
Int J Breast Cancer. 2012;2012:415170. doi: 10.1155/2012/415170. Epub 2012 May 9.
HER2-positive breast cancers have poorer prognosis and are prime candidates for molecular-targeted therapy because they are driven by the unique mechanism of HER2 oncogene addiction. While anti-HER2 agents such as trastuzumab and lapatinib are integral to the treatment of HER2-positive breast cancer, intrinsic and secondary resistance pose a significant challenge, underscoring the need to develop novel anti-HER2 therapies. In recent years, an array of promising and novel anti-HER2 therapeutic agents and their combinations have entered various stages of clinical development. However, questions remain on the optimal sequences of HER2-directed therapies and selection of patients for the most appropriate drug or combinations; incompletely defined mechanisms of trastuzumab action and resistance have also dampened the progress of more successful biomarker-driven treatment approaches. This paper summarizes existing preclinical and clinical evidence on the mechanisms of trastuzumab action and resistance and provides an up-to-date overview of novel HER2-directed therapies in clinical development.
人表皮生长因子受体2(HER2)阳性乳腺癌的预后较差,是分子靶向治疗的主要对象,因为它们是由HER2致癌基因成瘾的独特机制驱动的。虽然抗HER2药物如曲妥珠单抗和拉帕替尼是HER2阳性乳腺癌治疗的重要组成部分,但内在和继发性耐药构成了重大挑战,这突出了开发新型抗HER2疗法的必要性。近年来,一系列有前景的新型抗HER2治疗药物及其联合方案已进入不同阶段的临床开发。然而,关于HER2导向治疗的最佳顺序以及为最合适的药物或联合方案选择患者的问题仍然存在;曲妥珠单抗作用和耐药机制尚未完全明确,这也阻碍了更成功的生物标志物驱动治疗方法的进展。本文总结了关于曲妥珠单抗作用和耐药机制的现有临床前和临床证据,并提供了临床开发中新型HER2导向治疗的最新概述。