晚期非小细胞肺癌中的 MET 改变。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-04-01 DOI:10.1016/j.currproblcancer.2024.101075
Gabriel Cavalcante Lima Chagas , Amanda Ribeiro Rangel , Badi El Osta
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引用次数: 0

摘要

精准医疗帮助确定了几种可通过靶向疗法治疗的肿瘤分子畸变。这些疗法对具有特定致癌驱动因素的晚期癌症患者的疗效有显著提高,且无过多毒性。在转移性肺癌中,广泛的肿瘤分子测序平台的应用帮助肿瘤医疗机构确定了与前期靶向疗法治疗效果更好相关的致癌驱动因素。多达60%的非小细胞肺癌存在间充质-上皮转化因子(MET)改变,并与不良预后有关。目前,卡马替尼和泰泊替尼是美国食品和药物管理局(FDA)批准的仅有的两种针对MET 14外显子跳越突变患者的靶向疗法。目前正在开发几种药物,以满足 MET 基因改变患者的未满足需求。其中一些药物正与表皮生长因子受体靶向治疗联合使用,以减轻对表皮生长因子受体抑制剂的耐药性。这些药物有望为这些患者带来新的希望。
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MET alterations in advanced non-small cell lung cancer

Precision medicine has helped identify several tumor molecular aberrations to be treated with targeted therapies. These therapies showed substantial improvement in efficacy without excessive toxicity in patients with specific oncogenic drivers with advanced cancers. In metastatic lung cancers, the implementation of broad platforms for molecular tumor sequencing has helped oncology providers identify oncogenic drivers linked with better outcomes when treated upfront with targeted therapies. Mesenchymal-epithelial transition factor (MET) alterations are present in up to 60% of non-small cell lung cancer and are associated with a poor prognosis. Capmatinib and tepotinib are currently the only two approved targeted therapies by the U.S. Food and Drug Administration (FDA) for patients with MET exon 14 skipping mutation. Several agents are being developed to tackle an unmet need in patients with MET alterations. Some of these agents are being used in combination with EGFR targeted therapy to mitigate resistance to EGFR inhibitor. These agents are poised to provide new hope for these patients.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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