[预测病理学在肿瘤学中的作用——以EGFR为靶点的新疗法为例]。

Arndt Hartmann
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引用次数: 0

摘要

新的癌症特异性治疗是基于恶性肿瘤的特异性分子改变,这些改变是由小抑制分子或特异性抗体靶向的。在这些药物的开发过程中,潜在的分子靶点因其表达和对疾病发病机制和临床病程的重要性而具有特点。通常假设目标蛋白的表达程度或目标基因的分子改变允许预测某个患者是否会从针对该特定蛋白的治疗中获益。第一个例子是Her-2过表达和/或扩增的乳腺癌患者对Her-2特异性抗体(赫赛汀)治疗有反应。表皮生长因子受体(EGFR, Her-1)的表达或激活在许多上皮肿瘤中发生改变,临床研究表明它们在肿瘤的病因和进展中起重要作用。几种egfr特异性单克隆抗体和特异性酪氨酸激酶抑制剂在过去几年被开发出来。西妥昔单抗被批准用于治疗转移性结直肠癌和头颈部晚期鳞状细胞癌,并在许多其他肿瘤的试验中进行了研究。在第一次试验中,肿瘤中EGFR的表达是治疗的先决条件,使病理学家在治疗决策中发挥核心作用。然而,最近的数据清楚地表明,EGFR表达的程度与治疗反应无关。因此,不应仅仅因为肿瘤中缺乏EGFR表达而拒绝对个别患者进行治疗。酪氨酸激酶抑制剂(如吉非替尼、厄洛替尼)在治疗非小细胞肺癌方面是有效的,并且在许多癌症类型的正在进行的试验中也进行了研究。治疗反应与特异性分子改变(EGFR酪氨酸激酶结构域突变)和临床病理特征(亚洲种族、女性、非吸烟者、细支气管肺泡分化)的相关性是未来预测分子病理学潜在作用的一个很好的例子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Role of predictive pathology in oncology--example of new therapies targeting EGFR].

New cancer-specific therapies are based on specific molecular alterations of malignant tumors which are targeted by small inhibitory molecules or specific antibodies. During the development of these agents potential molecular targets are characterized for their expression and importance for pathogenesis and clinical course of the disease. Frequently the assumption is made that the degree of expression of the target protein or the molecular alteration of the target gene allows a prediction if a certain patient will profit from the therapy against this specific protein or not. The first example was that breast cancer patients with overexpression and/or amplification of Her-2 respond to a Her-2-specific antibody (Herceptin) therapy. The expression or activation of the Epidermal Growth Factor Receptor (EGFR, Her-1) are altered in many epithelial tumours and clinical studies indicate that they have important roles in tumor aetiology and progression. Several EGFR-specific monoclonal antibodies and specific tyrosine kinase inhibitors were developed in the last years. Cetuximab is approved for the treatment of metastatic colorectal cancer and advanced squamous cell carcinoma of the head and neck and is investigated in numerous trials for other tumors. The expression of EGFR in the tumor was a prerequisite for the therapy in the first trials, giving the pathologist a central role in treatment decision. However, recent data clearly demonstrate that the degree of EGFR expression does not correlate with therapy response. Therefore a therapy should be not denied to a individual patient solely because of lack of EGFR expression in the tumor. Tyrosine kinase inhibitors (e. g. Gefitinib, Erlotinib) are effective in the treatment of non small cell lung cancer and also investigated in ongoing trials in many cancer types. The correlation of therapy response with both specific molecular alterations (EGFR tyrosine kinase domain mutations) and clinicopathological features (Asian ethnicity, women, non-smokers, bronchioloalveolar differentation) is a good example of the potential role of predictive molecular pathology in the future.

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