非小细胞肺癌的免疫治疗和靶向治疗

Q4 Medicine
T. Nguyen-Ngoc, M. Reck, D. Tan, S. Peters
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引用次数: 5

摘要

在过去的十年中,靶向治疗的出现改变了非小细胞肺癌(NSCLC)的治疗模式。针对特定基因改变的治疗方法越来越多,如表皮生长因子(EGFR)突变和间变性淋巴瘤激酶(ALK)重排,导致指南发生变化,以反映分子谱分析的需求。最近,免疫治疗方法已经在非小细胞肺癌的治疗环境中进行了研究,与化疗相比,这些方法可能提供更好的结果,并且具有更好的耐受性。目前可用于非小细胞肺癌的免疫疗法包括检查点抑制剂抗pd -1抗体纳武单抗和派姆单抗。其他几种抗pd - l1化合物,如atezolizumab、durvalumab和avelumab,在所有治疗线的临床研究、单药治疗以及与免疫启动期激活剂抗ctla4易普利姆单抗和tremelimumab联合使用中也处于非常先进的水平。肿瘤学家面临的挑战是确定哪种治疗方法最适合个体患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immunotherapy and Targeted Therapies in the Treatment of Non-small Cell Lung Cancer
I n the last decade, the emergence of targeted therapies has changed the treatment paradigm for non-small cell lung cancer (NSCLC). The growing availability of therapies targeting specific genetic alterations, such as epidermal growth factor (EGFR) mutations and anaplastic lymphoma kinase (ALK) rearrangements, have led to changes in the guidelines to reflect the need for molecular profiling. More recently, immunotherapeutic approaches have been investigated in the treatment setting of NSCLC, and these may provide superior outcomes and have substantially better tolerability compared to chemotherapy. Immunotherapies currently available for NSCLC include the checkpoint inhibitors anti-PD-1 antibodies nivolumab and pembrolizumab. Several other anti-PD-L1 compounds such as atezolizumab, durvalumab and avelumab are also very advanced in clinical investigation, in monotherapy as well as in combination with immune priming phase activators anti-CTLA4 ipilimumab and tremelimumab, across all treatment lines. The challenge facing oncologists is identifying which therapy is best suited to the individual patient.
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来源期刊
European Oncology and Haematology
European Oncology and Haematology Medicine-Hematology
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