Molecular Biology of Lung Cancer Diagnosis and Management of Lung Cancer, 3rd ed: American College of Chest Physicians Evidence-Based Clinical Practice Guidelines

被引:54
|
作者
Nana-Sinkam, Serge Patrick [1 ]
Powell, Charles A. [2 ]
机构
[1] Ohio State Univ, Div Pulm Allergy Crit Care & Sleep Med, Columbus, OH 43210 USA
[2] Mt Sinai Sch Med, Div Pulm Crit Care & Sleep Med, New York, NY 10029 USA
关键词
IN-SITU HYBRIDIZATION; GENE COPY NUMBER; RANDOMIZED PHASE-II; EGFR MUTATION; STEM-CELLS; PROMOTER HYPERMETHYLATION; ADJUVANT CHEMOTHERAPY; ACTIVATING MUTATIONS; PROTEIN EXPRESSION; TUMOR PROGRESSION;
D O I
10.1378/chest.12-2346
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Based on recent bench and clinical research, the treatment of lung cancer has been refined, with treatments allocated according to histology and specific molecular features. For example, targeting mutations such as epidermal growth factor receptor (EGFR) with tyrosine kinase inhibitors has been particularly successful as a treatment modality, demonstrating response rates in selected patients with adenocarcinoma tumors harboring EGFR mutations that are significantly higher than those for conventional chemotherapy. However, the development of new targeted therapies is, in part, highly dependent on an improved understanding of the molecular underpinnings of tumor initiation and progression, knowledge of the role of molecular aberrations in disease progression, and the development of highly reproducible platforms for high-throughput biomarker discovery and testing. In this article, we review clinically relevant research directed toward understanding the biology of lung cancer. The clinical purposes of this research are (1) to identify susceptibility variants and field molecular alterations that will promote the early detection of tumors and (2) to identify tumor molecular alterations that serve as therapeutic targets, prognostic biomarkers, or predictors of tumor response. We focus on research developments in the understanding of lung cancer somatic DNA mutations, chromosomal aberrations, epigenetics, and the tumor microenvironment, and how they can advance diagnostics and therapeutics.
引用
收藏
页码:E30 / E39
页数:10
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