Sendur Mehmet Ali Nahit, Aksoy Sercan, Özdemir Nuriye Yildirim, Zengin Nurullah, Altundağ Kadri
Ankara Numune Education and Research Hospital, and Department of Medical Oncology, Hacettepe University Institute of Oncology, Ankara, Turkey.
Asian Pac J Cancer Prev. 2012;13(11):5915-6.
Human epidermal growth factor receptor (HER) 2 overexpression, observed in 20-25 percent of invasive breast cancers, is well known to be associated with a more aggressive phenotype and poor prognosis, with resistance to certain chemotherapeutic agents. The majority of patients with metastatic breast cancer who initially respond to trastuzumab, demonstrate disease progression within 1 year of treatment initiation. Furthermore, lack of response in some patients and relapse during the course of therapy, continue to challenge researchers and clinicians. A better understanding of the fundamental mechanisms of trastuzumab action is required so that new therapies directed at HER2 can be developed. We present here findings for mechanisms, both of Trastuzumab action and clinical resistance or escape.
人表皮生长因子受体(HER)2过表达见于20%-25%的浸润性乳腺癌,众所周知,其与更具侵袭性的表型、预后不良以及对某些化疗药物耐药有关。大多数最初对曲妥珠单抗有反应的转移性乳腺癌患者,在开始治疗后1年内会出现疾病进展。此外,一些患者无反应以及治疗过程中复发,仍然是研究人员和临床医生面临的挑战。需要更好地理解曲妥珠单抗作用的基本机制,以便开发针对HER2的新疗法。我们在此展示曲妥珠单抗作用机制以及临床耐药或逃逸方面的研究结果。