A Personalized Treatment for Lung Cancer: Molecular Pathways, Targeted Therapies, and Genomic Characterization

被引:95
作者
Hensing, Thomas [1 ,2 ]
Chawla, Apoorva [2 ]
Batra, Rishi [3 ]
Salgia, Ravi [2 ]
机构
[1] NorthShore Univ Hlth Syst, Kellogg Canc Ctr, Hematol Oncol Sect, Dept Med, Evanston, IL 60201 USA
[2] Univ Chicago, Dept Med, Hematol Oncol Sect, Chicago, IL 60637 USA
[3] Univ Nebraska Med Ctr, Omaha, NE 68198 USA
来源
SYSTEMS ANALYSIS OF HUMAN MULTIGENE DISORDERS | 2014年 / 799卷
关键词
TYROSINE KINASE INHIBITOR; SYNTHETIC LETHAL INTERACTION; TRIALIST ASSOCIATION ANITA; EML4-ALK FUSION GENE; PHASE-II TRIAL; ACQUIRED-RESISTANCE; ADJUVANT CHEMOTHERAPY; MET AMPLIFICATION; KRAS MUTATIONS; RAS ONCOGENE;
D O I
10.1007/978-1-4614-8778-4_5
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Lung cancer is a heterogeneous, complex, and challenging disease to treat. With the arrival of genotyping and genomic profiling, our simple binary division of lung cancer into non-small-cell lung cancer (NSCLC) and small-cell lung cancer (SCLC) is no longer acceptable. In the past decade and with the advent of personalized medicine, multiple advances have been made in understanding the underlying biology and molecular mechanisms of lung cancer. Lung cancer is no longer considered a single disease entity and is now being subdivided into molecular subtypes with dedicated targeted and chemotherapeutic strategies. The concept of using information from a patient's tumor to make therapeutic and treatment decisions has revolutionized the landscape for cancer care and research in general. Management of non-small-cell lung cancer, in particular, has seen several of these advances, with the understanding of activating mutations in EGFR, fusion genes involving ALK, rearrangements in ROS-1, and ongoing research in targeted therapies for K-RAS and MET. The next era of personalized treatment for lung cancer will involve a comprehensive genomic characterization of adenocarcinoma, squamous-cell carcinoma, and small-cell carcinoma into various subtypes. Future directions will involve incorporation of molecular characteristics and next generation sequencing into screening strategies to improve early detection, while also having applications for joint treatment decision making in the clinics with patients and practitioners. Personalization of therapy will involve close collaboration between the laboratory and the clinic. Given the heterogeneity and complexity of lung cancer treatment with respect to histology, tumor stage, and genomic characterization, mind mapping has been developed as one of many tools which can assist physicians in this era of personalized medicine. We attempt to utilize the above tool throughout this chapter, while reviewing lung cancer epidemiology, lung cancer treatment, and the genomic characterization of lung cancer.
引用
收藏
页码:85 / 117
页数:33
相关论文
共 133 条
[1]   Reduced Lung-Cancer Mortality with Low-Dose Computed Tomographic Screening [J].
Aberle, Denise R. ;
Adams, Amanda M. ;
Berg, Christine D. ;
Black, William C. ;
Clapp, Jonathan D. ;
Fagerstrom, Richard M. ;
Gareen, Ilana F. ;
Gatsonis, Constantine ;
Marcus, Pamela M. ;
Sicks, JoRean D. .
NEW ENGLAND JOURNAL OF MEDICINE, 2011, 365 (05) :395-409
[2]   Effect of Disrupting Seven-in-Absentia Homolog 2 Function on Lung Cancer Cell Growth [J].
Ahmed, Atique U. ;
Schmidt, Rebecca L. ;
Park, Cheol Hong ;
Reed, Nanette R. ;
Hesse, Shayla E. ;
Thomas, Charles F. ;
Molina, Julian R. ;
Deschamps, Claude ;
Yang, Ping ;
Aubry, Marie C. ;
Tang, Amy H. .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2008, 100 (22) :1606-1629
[3]   Who is at high risk for lung cancer? Population-level and individual-level perspectives [J].
Alberg, Anthony J. ;
Nonemaker, Jill .
SEMINARS IN RESPIRATORY AND CRITICAL CARE MEDICINE, 2008, 29 (03) :223-232
[4]  
Altekruse S F., SEER CANC STAT REV 1
[5]  
[Anonymous], 2012, CANC FACTS FIG
[6]  
[Anonymous], J CLIN ONCOL S
[7]   Rebiopsy of Lung Cancer Patients with Acquired Resistance to EGFR Inhibitors and Enhanced Detection of the T790M Mutation Using a Locked Nucleic Acid-Based Assay [J].
Arcila, Maria E. ;
Oxnard, Geoffrey R. ;
Nafa, Khedoudja ;
Riely, Gregory J. ;
Solomon, Stephen B. ;
Zakowski, Maureen F. ;
Kris, Mark G. ;
Pao, William ;
Miller, Vincent A. ;
Ladanyi, Marc .
CLINICAL CANCER RESEARCH, 2011, 17 (05) :1169-1180
[8]   Benefits and Harms of CT Screening for Lung Cancer A Systematic Review [J].
Bach, Peter B. ;
Mirkin, Joshua N. ;
Oliver, Thomas K. ;
Azzoli, Christopher G. ;
Berry, Donald A. ;
Brawley, Otis W. ;
Byers, Tim ;
Colditz, Graham A. ;
Gould, Michael K. ;
Jett, James R. ;
Sabichi, Anita L. ;
Smith-Bindman, Rebecca ;
Wood, Douglas E. ;
Qaseem, Amir ;
Detterbeck, Frank C. .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2012, 307 (22) :2418-2429
[9]   Systematic RNA interference reveals that oncogenic KRAS-driven cancers require TBK1 [J].
Barbie, David A. ;
Tamayo, Pablo ;
Boehm, Jesse S. ;
Kim, So Young ;
Moody, Susan E. ;
Dunn, Ian F. ;
Schinzel, Anna C. ;
Sandy, Peter ;
Meylan, Etienne ;
Scholl, Claudia ;
Froehling, Stefan ;
Chan, Edmond M. ;
Sos, Martin L. ;
Michel, Kathrin ;
Mermel, Craig ;
Silver, Serena J. ;
Weir, Barbara A. ;
Reiling, Jan H. ;
Sheng, Qing ;
Gupta, Piyush B. ;
Wadlow, Raymond C. ;
Le, Hanh ;
Hoersch, Sebastian ;
Wittner, Ben S. ;
Ramaswamy, Sridhar ;
Livingston, David M. ;
Sabatini, David M. ;
Meyerson, Matthew ;
Thomas, Roman K. ;
Lander, Eric S. ;
Mesirov, Jill P. ;
Root, David E. ;
Gilliland, D. Gary ;
Jacks, Tyler ;
Hahn, William C. .
NATURE, 2009, 462 (7269) :108-U122
[10]   Acquired Resistance to Epidermal Growth Factor Receptor Kinase Inhibitors Associated with a Novel T854A Mutation in a Patient with EGFR-Mutant Lung Adenocarcinoma [J].
Bean, James ;
Riely, Gregory J. ;
Balak, Marissa ;
Marks, Jenifer L. ;
Ladanyi, Marc ;
Miller, Vincent A. ;
Pao, William .
CLINICAL CANCER RESEARCH, 2008, 14 (22) :7519-7525