Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/20799
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dc.contributor.authorSilagy, Andrew W-
dc.contributor.authorSanchez, Alejandro-
dc.contributor.authorManley, Brandon J-
dc.contributor.authorBensalah, Karim-
dc.contributor.authorBex, Axel-
dc.contributor.authorKaram, Jose A-
dc.contributor.authorLjungberg, Börje-
dc.contributor.authorShuch, Brian-
dc.contributor.authorHakimi, A Ari-
dc.date2019-04-27-
dc.date.accessioned2019-05-17T00:25:33Z-
dc.date.available2019-05-17T00:25:33Z-
dc.date.issued2019-11-
dc.identifier.citationEuropean Urology Focus 2019; 5(6): 949-957-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/20799-
dc.description.abstractSmall renal masses (SRMs; tumors <4 cm) encompass a diagnostic and therapeutic challenge. Genomic profiling has the potential to improve risk stratification and personalize treatment selection. Herein, we review the evidence regarding the utility, challenges, and potential implications of genomic profiling in the management of SRMs. Pertinent publications available on PubMed database pertaining to kidney cancer, tumor size, genomics, and clinical management were reviewed. Compared with larger tumors, SRMs range from benign to lethal, necessitating strategies for improved treatment selection. Recent advances in the molecular characterization of renal cell carcinoma have improved our understanding of the disease; however, utility of these tools for the management of SRMs is less clear. While intratumoral heterogeneity (ITH) reduces the accuracy and reliability of sequencing, relative genomic uniformity of SRMs somewhat lessens the impact of ITH. Therefore, renal mass biopsy of SRMs represents an appealing opportunity to evaluate how incorporation of molecular profiles may improve management strategies. Ongoing research into the genomic landscape of SRMs has advanced our understanding of the spectrum of disease aggressiveness and may hold promise in matching disease biology to treatment intensity. Small renal masses are a clinical challenge, as they range from benign to lethal. Genomic profiling may eventually improve treatment selection, but more research is needed.-
dc.language.isoeng-
dc.subjectBiopsy-
dc.subjectGenomics-
dc.subjectHeterogeneity-
dc.subjectKidney cancer-
dc.subjectRenal cell carcinoma-
dc.subjectSmall renal mass-
dc.titleHarnessing the Genomic Landscape of the Small Renal Mass to Guide Clinical Management.-
dc.typeJournal Article-
dc.identifier.journaltitleEuropean urology focus-
dc.identifier.affiliationUCLA School of Medicine, Los Angeles, CA, USAen
dc.identifier.affiliationThe Netherlands Cancer Institute, Amsterdam, The Netherlandsen
dc.identifier.affiliationUrology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USAen
dc.identifier.affiliationMoffitt Cancer Center Genitourinary Oncology and Integrated Mathematical Oncology, Tampa, FL, USAen
dc.identifier.affiliationDepartment of Urology, The University of Texas MD Anderson Cancer Center, Houston, TX, USAen
dc.identifier.affiliationRoyal Free London NHS Foundation Trust and UCL Division of Surgery and Interventional Science, London, UKen
dc.identifier.affiliationUrology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USAen
dc.identifier.affiliationDepartment of Urology, University of Rennes, Rennes, France-
dc.identifier.affiliationDepartment of Surgical and Perioperative Sciences, Umeå University, Umeå, Sweden-
dc.identifier.affiliationDepartment of Surgery, Austin Health, The University of Melbourne, Heidelberg, Victoria, Australia-
dc.identifier.doi10.1016/j.euf.2019.04.011-
dc.identifier.pubmedid31040082-
dc.type.austinJournal Article-
dc.type.austinReview-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
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