癌症研究档案

  • 国际标准期刊号: 2254-6081
  • 期刊 h 指数: 13
  • 期刊引用分数: 3.58
  • 期刊影响因子: 3.12
索引于
  • 中国知网(CNKI)
  • 引用因子
  • OCLC-WorldCat
  • 普布隆斯
  • 日内瓦医学教育与研究基金会
  • 谷歌学术
  • 秘密搜索引擎实验室
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Clinical Challenges to Current Molecularly Targeted Therapies in CellularBreakdown in the Lungs

Shinji Osada, Satoshi Matsui, Yoshiyuki Sasaki

The Cellular breakdown in the lungs is hard to treat with ahelpless guess and a long term endurance of 15%. Currentatomically focused on treatments are at first viable in non-little cell cellular breakdown in the lungs (NSCLC) patients;be that as it may, they are tormented with troublesincluding instigatedobstruction and little remediallyresponsive populaces. This scaled down audit portrays theinstrument of protection from a few atomically focused ontreatments which are at present being utilized to treatNSCLC. The significant targets talked about are c-Met, EGFR,HER2, ALK, VEGFR, and BRAF. The original tyrosine kinaseinhibitors (TKIs) brought about obstruction; nonetheless,second and third era TKIs are being created, which are forthe most part more useful and can possibly treat NSCLCpatients with protection from original TKIs. Blendtreatments could likewise be compelling in forestalling TKIopposition in NSCLC patients.

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