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SCI 발표논문

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Expert Rev Mol Diagn. 2007;7(6):821-36.

Chasing targets for EGFR tyrosine kinase inhibitors in non-small-cell lung cancer: Asian perspectives.

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제1저자 김태유 · 교신저자 방영주

PMID 18020911 DOI 10.1586/14737159.7.6.821 IF 4.3 혈액종양내과
소속 (1)
  1. Seoul National University Hospital, Department of Internal Medicine, Cancer Research Institute, Seoul National University College of Medicine, 28 Yongon-Dong, Chongno-Gu, Seoul, 110-744, Korea.

Abstract

EGF receptor (EGFR) activation has an important role in various steps of carcinogenesis and progression of non-small-cell lung cancer (NSCLC), implying that EGFR is a potential target for cancer therapy. Therefore, targeted treatments aimed at EGFR have been developed, of which tyrosine kinase inhibitors (TKIs), gefitinib and erlotinib have shown activity in NSCLC. The unexpected findings of a lack of association between expression of EGFR, the target and efficacy of EGFR TKIs and higher response in selective subgroups of patients were puzzling. Identification of somatic activating mutations in the EGFR tyrosine kinase domain solved the mystery and provided new insight. Several lines of study provided information on various molecular targets for EGFR TKI therapy. A target-based patient-selection strategy is expected to eventually lead to tailored therapy for lung cancer.

그 밖의 정보
출판 형태
Journal Article, Research Support, Non-U.S. Gov't, Review
저널
Expert review of molecular diagnostics · eISSN 1744-8352
MeSH
Antineoplastic Agents / metabolism / therapeutic use · Asian People / genetics · Biomarkers, Tumor / metabolism · Carcinoma, Non-Small-Cell Lung* / drug therapy / metabolism / pathology · Clinical Trials as Topic · ErbB Receptors / antagonists & inhibitors / genetics / metabolism · Erlotinib Hydrochloride · Gefitinib · Gene Dosage · Humans · Mutation · Polymorphism, Genetic · Protein Kinase Inhibitors / metabolism / therapeutic use · Quinazolines / metabolism / therapeutic use
Substances
Antineoplastic Agents · Biomarkers, Tumor · Protein Kinase Inhibitors · Quinazolines · Erlotinib Hydrochloride · ErbB Receptors · Gefitinib