曲妥珠单抗-emtansine (TDM1)在her2阳性乳腺癌脑转移中的活性:一个病例系列

Kevin C. Keith , Yueh Lee , Matthew G. Ewend , Timothy M. Zagar , Carey K. Anders
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引用次数: 36

摘要

乳腺癌脑转移(BCBM)的发病率正在增加,部分原因是全身性疾病管理的改善和生存期的延长。尽管患者人数不断增加,但对于her2阳性BCBM的治疗方法却几乎没有共识。拉帕替尼是唯一一种治疗her2阳性癌症的脑渗透性靶向药物,其颅内反应率有限,对her2阳性患者的无进展生存期(PFS)改善甚微。尺寸限制被认为会阻止较大的单克隆抗体,如帕妥珠单抗和曲妥珠单抗,通过血脑屏障(BBB)。然而,新出现的证据表明,血脑屏障在转移环境中受到干扰,从而提高了这些较大靶向药物的外显率。破坏的血脑屏障可能允许阿多-曲妥珠单抗emtansine (TDM1)通过,尽管目前关于其在BCBM患者中的活性的临床信息知之甚少。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Activity of trastuzumab-emtansine (TDM1) in HER2-positive breast cancer brain metastases: A case series

The incidence of breast cancer brain metastasis (BCBM) is increasing due in part to improved management of systemic disease and prolonged survival. Despite this growing population of patients, there exists little consensus for the treatment of HER2-positive BCBM. Lapatinib, the only brain permeable targeted agent for HER2-positive cancer, has demonstrated limited intracranial response rates and little improvement in progression free survival (PFS) for HER-2 positive patients. Size constraints are believed to prevent larger monoclonal antibodies, such as pertuzumab and trastuzumab, from crossing the blood brain barrier (BBB). However, emerging evidence reveals that the BBB is perturbed in the setting of metastases, allowing for improved penetrance of these larger targeted agents. The disrupted BBB may allow for passage of ado-trastuzumab emtansine (TDM1), though little clinical information about its activity in BCBM patients is currently known.

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