摘要
ErbB蛋白家族的过度激活,这是由4种络氨酸激酶成员(ErbB1/表皮生长因子受体[EGFR]/HER1、ErbB2/HER2、ErbB3/HER3 和 ErbB4/HER4)组成,可以启动多种恶性肿瘤的发展和恶化,包括结肠癌、头部和颈部癌症和某些非小细胞肺癌(NSCLCs)。因此,靶向ErbB家族中特定成员的药物已经被开发用作癌症治疗。这些药物包括可逆的EGFR络氨酸激酶抑制剂(TKIs)埃罗替尼和吉非替尼;EGFR-靶向单克隆抗体西妥昔单抗和帕尼单抗;和HER2-靶向单克隆抗体曲妥单抗。拉帕替尼是一个靶向EGFR和HER2的双TKI。此外,TKIs抑制多个ErbB家族成员并不可逆地结合他们的靶标,现用于癌症治疗的评估。三个此类化合物已发展至临床研究: EGFR、 HER2,和HER4抑制剂afatinib、 dacomitinib,和neratinib。这些药物的I期研究表明其在NSCLC、乳腺癌和其他恶性肿瘤中有临床活性。近期,afatinib被批准用于EGFR突变-阳性NSCLC,并被开发用于鳞状 NSCLC;dacomitinib在III期临床中被用于NSCLC,;neratinib在III期临床中被用于乳腺癌的治疗,afatinib也在III期临床中被用于头部和颈部癌症。临床试验的最终结果可能致使这些药物被批准用于治疗多种实体恶性肿瘤。
关键词: Afatinib
图形摘要
Current Cancer Drug Targets
Title:Irreversible Multitargeted ErbB Family Inhibitors for Therapy of Lung and Breast Cancer
Volume: 14 Issue: 9
Author(s): Deepa Subramaniam, Aiwu Ruth He, Jimmy Hwang, John Deeken, Michael Pishvaian, Marion L. Hartley and John L. Marshall
Affiliation:
关键词: Afatinib
摘要: Overactivation of the ErbB protein family, which is comprised of 4 receptor tyrosine kinase members (ErbB1/epidermal growth factor receptor [EGFR]/HER1, ErbB2/HER2, ErbB3/HER3, and ErbB4/HER4), can drive the development and progression of a wide variety of malignancies, including colorectal, head and neck, and certain non–small cell lung cancers (NSCLCs). As a result, agents that target a specific member of the ErbB family have been developed for the treatment of cancer. These agents include the reversible EGFR tyrosine kinase inhibitors (TKIs) erlotinib and gefitinib; the EGFR-targeting monoclonal antibodies cetuximab and panitumumab; and the HER2-targeting monoclonal antibody trastuzumab. Lapatinib is a dual TKI that targets both EGFR and HER2. In addition, TKIs that inhibit multiple members of the ErbB family and also bind their targets irreversibly are under evaluation for the treatment of cancer. Three such compounds have progressed into clinical studies: the EGFR, HER2, and HER4 inhibitors afatinib, dacomitinib, and neratinib. Phase I studies of these agents have shown clinical activity in NSCLC, breast cancer, and other malignancies. Currently, afatinib is approved for EGFR mutation-positive NSCLC and is in development for squamous NSCLC, and dacomitinib is in phase III of clinical development for NSCLC, neratinib is in phase III of clinical development for the treatment of breast cancer, and afatinib is also in phase III development in head and neck cancer. Final results from clinical trials may lead to the potential approval of these agents in a variety of solid tumor malignancies.
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Cite this article as:
Deepa Subramaniam, Aiwu Ruth He, Jimmy Hwang, John Deeken, Michael Pishvaian, Marion L. Hartley and John L. Marshall , Irreversible Multitargeted ErbB Family Inhibitors for Therapy of Lung and Breast Cancer, Current Cancer Drug Targets 2014; 14 (9) . https://dx.doi.org/10.2174/1568009614666141111104643
DOI https://dx.doi.org/10.2174/1568009614666141111104643 |
Print ISSN 1568-0096 |
Publisher Name Bentham Science Publisher |
Online ISSN 1873-5576 |
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