Transitioning Discoveries from Cancer Genomics Research Laboratories into Pathology Practice

作者: Tamara Jamaspishvili , Jeremy A. Squire

DOI: 10.1007/978-1-4939-0727-4_12

关键词:

摘要: Genomic biomarkers are increasingly being used for detection of cancer, recognizing early disease recurrence, or to provide crucial molecular findings essential the use novel classes targeting therapies. Although there is considerable enthusiasm discoveries cancer genomics personalized medicine in clinical practice, number new incorporated into diagnosis and treatment remains surprisingly low. In this chapter we describe how laboratory approaches research usually move pathology consider why uptake genomic has been so slow. We illustrate by describing some genetic tests that successfully practice now. draw attention challenges faced delivering practice-changing discoveries; discuss potential impact on design trials. Finally, review current guidelines recommendations moving a successful biomarker from practice.

参考文章(102)
Victor Trevino, Francesco Falciani, Hugo A. Barrera-Saldaña, DNA microarrays: a powerful genomic tool for biomedical and clinical research. Molecular Medicine. ,vol. 13, pp. 527- 541 ,(2007) , 10.2119/2006-00107.TREVINO
Yuri E. Nikiforov, Molecular Diagnostics of Thyroid Tumors Archives of Pathology & Laboratory Medicine. ,vol. 135, pp. 569- 577 ,(2011) , 10.1043/2010-0664-RAIR.1
Charles E. Massie, Ian G. Mills, Mapping protein-DNA interactions using ChIP-sequencing Methods of Molecular Biology. ,vol. 809, pp. 157- 173 ,(2012) , 10.1007/978-1-61779-376-9_11
Iris Schrijver, Nazneen Aziz, Daniel H. Farkas, Manohar Furtado, Andrea Ferreira Gonzalez, Timothy C. Greiner, Wayne W. Grody, Tina Hambuch, Lisa Kalman, Jeffrey A. Kant, Roger D. Klein, Debra G.B. Leonard, Ira M. Lubin, Rong Mao, Narasimhan Nagan, Victoria M. Pratt, Mark E. Sobel, Karl V. Voelkerding, Jane S. Gibson, Opportunities and challenges associated with clinical diagnostic genome sequencing: a report of the Association for Molecular Pathology. The Journal of Molecular Diagnostics. ,vol. 14, pp. 525- 540 ,(2012) , 10.1016/J.JMOLDX.2012.04.006
Tony Shen, Stefan Hans Pajaro-Van de Stadt, Nai Chien Yeat, Jimmy C.-H. Lin, Clinical applications of next generation sequencing in cancer: from panels, to exomes, to genomes Frontiers in Genetics. ,vol. 6, pp. 215- 215 ,(2015) , 10.3389/FGENE.2015.00215
, Recommendations on screening for cervical cancer. Canadian Medical Association Journal. ,vol. 185, pp. 35- 45 ,(2013) , 10.1503/CMAJ.121505
Tarek A. Bismar, Maisa Yoshimoto, Robin T. Vollmer, Qiuli Duan, Matthew Firszt, Jacques Corcos, Jeremy A. Squire, PTEN genomic deletion is an early event associated with ERG gene rearrangements in prostate cancer BJUI. ,vol. 107, pp. 477- 485 ,(2011) , 10.1111/J.1464-410X.2010.09470.X
Daniel J. Sargent, Barbara A. Conley, Carmen Allegra, Laurence Collette, Clinical Trial Designs for Predictive Marker Validation in Cancer Treatment Trials Journal of Clinical Oncology. ,vol. 23, pp. 2020- 2027 ,(2005) , 10.1200/JCO.2005.01.112
Loïc Le Marchand, Lynne R. Wilkens, Design considerations for genomic association studies: importance of gene-environment interactions. Cancer Epidemiology, Biomarkers & Prevention. ,vol. 17, pp. 263- 267 ,(2008) , 10.1158/1055-9965.EPI-07-0402