基因突变和人源化单克隆抗体治疗小细胞肺癌的研究进展

de Moraes Junior Rm, Mota Gs, Carolino Mlo, Kerche-Silva Le
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摘要

小细胞肺癌(SCLC)是肿瘤生长快、转移传播快的恶性肿瘤之一。与SCLC相关的最常见的基因修饰与肿瘤抑制基因和致癌基因有关,这些基因控制细胞的周期阻滞。SCLC的标准治疗是顺铂和依托泊苷等药物的联合治疗,有时也可以使用胸部放疗。但是这些治疗方法还不足以降低SCLC患者的死亡率,新的药物,特别是人源化单克隆抗体(mAb)已经被研究。因此,这项工作的目的是回顾SCLC的主要遗传改变和已经测试的单克隆抗体,以提高这些患者的预期寿命。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genetic Mutations and Humanized Monoclonal Antibody Treatment in Small-Cell Lung Cancer: A Review
Small-cell lung cancer (SCLC) is one of the deadliest type of cancer with fast tumor growth and rapid metastatic dissemination. The most common genetic modifications associated with SCLC is connected to tumor suppressor and oncogenic genes, genes that control the cycle arrest of the cells. Standard treatment for SCLC is a combination of drugs such as cisplatin and etoposide and sometimes radiotherapy of the chest can be used. But these treatments have not been sufficient to decrease dead rate in SCLC patients and new drugs have been studied, specially humanized monoclonal antibodies (mAb). Therefore, the aim of this work is to review the main genetic alterations in SCLC and the mAb that has been tested to improve life expectancy in these patients.
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