首页 | 本学科首页   官方微博 | 高级检索  
     


Genomic Testing in Patients with Metastatic Castration-resistant Prostate Cancer: A Pragmatic Guide for Clinicians
Authors:Axel S. Merseburger  Nick Waldron  Maria J. Ribal  Axel Heidenreich  Sven Perner  Karim Fizazi  Cora N. Sternberg  Joaquin Mateo  Manfred P. Wirth  Elena Castro  David Olmos  Daniel P. Petrylak  Simon Chowdhury
Affiliation:1. Lübeck University Hospital, Lübeck, Germany;2. Guy’s Hospital, London, UK;3. Hospital Clínic, University of Barcelona, Barcelona, Spain;4. Universitätsklinikum Köln, Cologne, Germany;5. Institute of Pathology, University Hospital Schleswig Holstein, Campus Lübeck, Lübeck, Germany;6. Pathology Research Center Borstel, Leibniz Lung Center, Borstel, Germany;7. University of Paris Institut Gustave Roussy, Villejuif Cedex, France;8. Englander Institute for Precision Medicine, Weill Cornell Medicine, New York-Presbyterian, New York, NY, USA;9. Vall d’Hebron Institute of Oncology, Vall d’Hebron University Hospital, Barcelona, Spain;10. University Hospital Carl Gustav Carus, Dresden, Germany;11. Spanish National Cancer Research Centre, Madrid, Spain;12. University Hospitals Regional and Virgen de la Victoria, Málaga, Spain;13. Yale University, Smilow Cancer Center, New Haven, CT, USA;14. Sarah Cannon Research Institute, London, UK
Abstract:ContextGenomic testing is becoming increasingly important in patients with advanced prostate cancer (PC) and is being incorporated in clinical practice to guide treatment.ObjectiveTo review the current understanding of genomic alterations and the status of genomic testing in patients with metastatic castration-resistant PC (mCRPC), and the potential use of genomic tests in clinical practice.Evidence acquisitionWe reviewed recent publications (past 15 yr) from PubMed, proceedings of scientific conferences, and published guidelines. Reports on mCRPC in the following areas were selected: development, testing, and validation of techniques for identifying genomic alterations; molecular characterization; and trials of genetically targeted therapies.Evidence synthesismCRPC tumors harbor molecular alterations that are possible targets for treatment, and a number of therapies are in development to exploit these alterations (eg, PD-1 inhibitors, PARP inhibitors, tyrosine kinase inhibitors). Next-generation sequencing of DNA from tumor tissue can identify somatic alterations that would not be identified by germline testing. Work is ongoing to evaluate the use of less invasive somatic testing methods (eg, sequencing of cell-free circulating tumor DNA). Current international guidelines recommend germline and/or somatic testing for men with advanced and/or high-risk PC regardless of family history to identify those with homologous recombination repair gene mutations or mismatch repair defects/microsatellite instability who may be eligible for treatment with a PARP inhibitor or pembrolizumab, respectively.ConclusionsGenomic testing for mCRPC may provide information on prognostic, predictive, and resistance biomarkers. Although the incorporation of testing into clinical practice remains challenging, routine genomic testing of men with advanced PC is recommended to guide management and treatment decisions.Patient summarySimilar to many cancers, prostate cancer is caused by defects in the cancer’s DNA, which are called genetic or genomic defects. New treatments targeting these defects are approved for metastatic castration-resistant prostate cancer. Specific new tests are under development to detect these potentially treatable genetic defects.
Keywords:Genomic testing  Metastatic castration-resistant prostate cancer  Next-generation sequencing  Tumor tissue  Circulating tumor cells  Circulating tumor DNA
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号