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Non-small cell lung cancer--genetic predictors

V. Koudelakova, M. Kneblova, R. Trojanec, J. Drabek, M. Hajduch

. 2013 ; 157 (2) : 125-136.

Language English Country Czech Republic

Document type Journal Article, Research Support, Non-U.S. Gov't, Review

Grant support
NT13569 MZ0 CEP Register

BACKGROUND: Non-small cell lung cancer (NSCLC) accounts for approximately 85% of all lung cancer that is the leading cause of cancer-related mortality worldwide. Several predictive markers have Been found in NSCLC patients to date But only a few are currently used for tailored therapy. METHODS AND RESULTS: Pu BMed and We B of Science online data Bases were used to search review and original articles on the most important predictive markers in NSCLC. CONCLUSION: EGFR activating mutations (exons 18 to 21) and EML4-ALK rearrangement are clinically important markers a Ble to select NSCLC patients which Benefit from EGFR or ALK tyrosine kinase inhi Bitors (gefitini B, erlotini B, crizotini B). Other markers, such as KRAS mutation, EGFR T790M mutation and C-MET amplification, are responsi Ble for resistance to these inhi Bitors. Overcoming of this resistance as well as discovery of new potential markers and inhi Bitors is the main goal of ongoing research and clinical trials in NSCLC.

References provided by Crossref.org

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$a BACKGROUND: Non-small cell lung cancer (NSCLC) accounts for approximately 85% of all lung cancer that is the leading cause of cancer-related mortality worldwide. Several predictive markers have Been found in NSCLC patients to date But only a few are currently used for tailored therapy. METHODS AND RESULTS: Pu BMed and We B of Science online data Bases were used to search review and original articles on the most important predictive markers in NSCLC. CONCLUSION: EGFR activating mutations (exons 18 to 21) and EML4-ALK rearrangement are clinically important markers a Ble to select NSCLC patients which Benefit from EGFR or ALK tyrosine kinase inhi Bitors (gefitini B, erlotini B, crizotini B). Other markers, such as KRAS mutation, EGFR T790M mutation and C-MET amplification, are responsi Ble for resistance to these inhi Bitors. Overcoming of this resistance as well as discovery of new potential markers and inhi Bitors is the main goal of ongoing research and clinical trials in NSCLC.
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