克拉斯
医学
肺癌
靶向治疗
精密医学
肿瘤科
表皮生长因子受体
个性化医疗
酪氨酸激酶
内科学
埃罗替尼
药品
生物信息学
表皮生长因子受体抑制剂
癌症研究
酪氨酸激酶抑制剂
癌症
受体酪氨酸激酶
转化研究
蛋白酪氨酸激酶
药物开发
仿形(计算机编程)
伴生诊断
肉瘤
ROS1型
激酶
药物重新定位
化疗
作者
Mayuri Mutukuru,Swathi Reddy Kandula,Veena Ramakrishna,Pravallika Sanka,Guna Priya Sidde,Shaik Mohammed Muzzamil,Hari Babu Uppara,P. Dharani Prasad
摘要
Abstract Lung cancer is a leading cause of cancer‐related mortality worldwide, accounting for approximately 13% of all diagnoses. Non‐small cell lung cancer (NSCLC) comprises 85% of lung cancer cases, with recent genetic profiling revealing the critical role of driver mutations in its pathogenesis. Advances in molecular stratification have redefined NSCLC classification, enabling targeted therapeutic approaches based on specific genetic abnormalities. Targeted therapies have shown significant clinical benefits, particularly in NSCLC patients with mutations in the epidermal growth factor receptor (EGFR), Kirsten rat sarcoma oncogene, and B‐Raf proto‐oncogene. These mutations are among the most prevalent actionable drivers, and treatments utilizing tyrosine kinase inhibitors (TKIs) have demonstrated substantial improvements in progression‐free survival compared to conventional chemotherapy. Emerging data suggest that TKI therapy may represent the optimal approach for advanced NSCLC with EGFR and KRAS mutations. This review highlights FDA‐approved therapies for NSCLC and examines recent clinical and translational research on EGFR and KRAS mutations. The findings underscore the pivotal role of personalized medicine and the potential of targeted therapies to transform treatment paradigms and improve patient outcomes in NSCLC.
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