Targeting the KRAS Pathway in Non-Small Cell Lung Cancer

被引:105
作者
Tomasini, Pascale [1 ]
Walia, Preet [1 ]
Labbe, Catherine [1 ]
Jao, Kevin [1 ]
Leighl, Natasha B. [1 ]
机构
[1] Univ Toronto, Div Med Oncol, Princess Margaret Canc Ctr, Toronto, ON, Canada
关键词
Non-small cell lung cancer; KRAS; Target; Pathway; MEK; Selumetinib; Trametinib; RANDOMIZED PHASE-II; GROWTH-FACTOR RECEPTOR; ANAPLASTIC LYMPHOMA KINASE; ORAL MEK INHIBITOR; ONCOGENIC K-RAS; DOSE-ESCALATION; AZD6244; ARRY-142886; OPEN-LABEL; 3-KINASE INHIBITOR; ANTITUMOR-ACTIVITY;
D O I
10.1634/theoncologist.2015-0084
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Lung cancer remains the leading cause of cancer-related deaths worldwide. However, significant progress has been made individualizing therapy based on molecular aberrations (e.g., EGFR, ALK) and pathologic subtype. KRAS is one of the most frequently mutated genes in non-small cell lung cancer (NSCLC), found in approximately 30% of lung adenocarcinomas, and is thus an appealing target for new therapies. Although no targeted therapy has yet been approved for the treatment of KRAS-mutant NSCLC, there are multiple potential therapeutic approaches. These may include direct inhibition of KRAS protein, inhibition of KRAS regulators, alteration of KRAS membrane localization, and inhibition of effector molecules downstream of mutant KRAS. This article provides an overview of the KRAS pathway in lung cancer and related therapeutic strategies under investigation.
引用
收藏
页码:1450 / 1460
页数:11
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