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Non-small cell lung cancer--genetic predictors
V. Koudelakova, M. Kneblova, R. Trojanec, J. Drabek, M. Hajduch
Language English Country Czech Republic
Document type Journal Article, Research Support, Non-U.S. Gov't, Review
Grant support
NT13569
MZ0
CEP Register
Digital library NLK
Full text - Article
Source
NLK
Directory of Open Access Journals
from 2001
Free Medical Journals
from 1998
Medline Complete (EBSCOhost)
from 2007-06-01
ROAD: Directory of Open Access Scholarly Resources
from 2001
PubMed
23733083
DOI
10.5507/bp.2013.034
Knihovny.cz E-resources
- MeSH
- Drug Resistance, Neoplasm MeSH
- ErbB Receptors drug effects genetics MeSH
- Oncogene Proteins, Fusion drug effects genetics MeSH
- Protein Kinase Inhibitors pharmacology MeSH
- Humans MeSH
- Biomarkers, Tumor genetics MeSH
- Lung Neoplasms drug therapy genetics MeSH
- Carcinoma, Non-Small-Cell Lung drug therapy genetics MeSH
- Proto-Oncogene Proteins c-met drug effects genetics MeSH
- Proto-Oncogene Proteins drug effects genetics MeSH
- ras Proteins drug effects genetics MeSH
- Protein-Tyrosine Kinases drug effects genetics MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Review MeSH
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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