Advances in the Management of Non-Small Cell Lung Cancer (NSCLC)

B. Khamar
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Abstract

Recent findings from studies [KEYNOTE 10, 24, 189, 407 (pembrolizumab); Check Mate-17,57,227 (nivolumab); IM power 131,150,OAK (atezolizumab)] using checkpoint inhibitors as a monotherapy as well as in combination of chemotherapy has demonstrated improved outcome in patients with advanced NSCLC without actionable mutation driver and also showed a tolerable toxicity profile and durable response. Based on analysis of studies performed in the first line management of advanced NSCLC, pembrolizumab is preferred for patients without actionable driver mutation. Pembrolizumab should be used as a monotherapy in patients with PD-L1 expression ≥ 50%. In others, it should be added to chemotherapy. For patients with actionable driver mutation, osimertinib for sensitizing EGFR mutation is preferred over afatinib, gefitinib, erlotinib as a first line therapy. For patients with ALK rearrangement alectinib is preferred over crizotinib restricting use of crizotinib as first line therapy to patients with ROS1 rearrangement. Dabrafenib + trametinib have been found effective in patients with BRAFV600E mutations.
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非小细胞肺癌(NSCLC)治疗进展
近期研究发现[KEYNOTE 10,24,189,407 (pembrolizumab);Check mate -17,57,227 (nivolumab);[m] power 131,150,OAK (atezolizumab)]使用检查点抑制剂作为单一疗法以及联合化疗,已经证明在没有可操作的突变驱动因素的晚期NSCLC患者中改善了结果,并且还显示出可耐受的毒性特征和持久的反应。基于对晚期非小细胞肺癌一线治疗研究的分析,派姆单抗优先用于无可操作驱动突变的患者。对于PD-L1表达≥50%的患者,Pembrolizumab应作为单药治疗。在其他情况下,它应该添加到化疗中。对于可操作的驱动突变患者,奥西替尼对EGFR突变的致敏性优于阿法替尼、吉非替尼、厄洛替尼作为一线治疗。ALK重排患者优先选择阿勒替尼而非克唑替尼,限制了ROS1重排患者使用克唑替尼作为一线治疗。Dabrafenib + trametinib已被发现对BRAFV600E突变患者有效。
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