转移性三阴性乳腺癌症中EGFR的抑制作用:一个失败的靶点

G. Hachem
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引用次数: 0

摘要

癌症是乳腺癌的一种组织学亚型,其特征是缺乏激素受体(HR)、人表皮生长因子受体2(HER2)的表达。15%的乳腺癌为三阴性。它是最具侵袭性的组织学亚型,影响年轻人群,尽管有足够的局部控制,但与远处复发高度相关,主要发生在诊断后的前三年。在转移性环境中,中位总生存期约为12个月。1,2唯一可用的治疗方法仍然包括传统的细胞毒性化疗,在过去十年中,聚ADP核糖聚合酶抑制剂(PARP)抑制剂取得了许多有希望的结果。转移性三阴性癌症(mTNBC)中表达的许多途径和受体一直是研究和临床试验的主题:雄激素受体、表皮生长因子受体(EGFR)、通过靶向某些表面受体的抗体-药物偶联物和抗血管生成药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
EGFR inhibition in metastatic triple negative breast cancer: a losing target
Triple negative breast cancer is a histologic subtype of breast carcinomas characterized by the lack of expression of hormone receptors (HR), human epidermal growth factor receptor 2 (HER2). Fifteen percent of the breast carcinomas are triple negative. It is the most aggressive histological subtype, affecting younger age population, and highly associated with distant recurrences despite adequate local control, mainly in the first three years following the diagnosis. In the metastatic setting, the median overall survival is around 12 months.1,2 The only available treatments still consist of conventional cytotoxic chemotherapy with many promising results seen with poly‒ADP‒ribose‒polymerase inhibitors (PARP) inhibitors during this last decade. Many pathways and receptors expressed in the metastatic triple negative breast cancer (mTNBC) had been the subjects of research and clinical trials: androgen receptors, epidermal growth factor receptor (EGFR), antibody drug conjugate via targeting certain surface receptors and anti‒angiogenics.
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