Cargando…

Comprehensive tumor profiling identifies numerous biomarkers of drug response in cancers of unknown primary site: Analysis of 1806 cases

BACKGROUND: Cancer of unknown primary (CUP) accounts for approximately 3% of all malignancies. Despite extensive laboratory and imaging efforts, the primary site usually cannot be unequivocally confirmed, and the treatment for the most part remains empirical. Recently, identification of common cance...

Descripción completa

Detalles Bibliográficos
Autores principales: Gatalica, Zoran, Millis, Sherri Z., Vranic, Semir, Bender, Ryan, Basu, Gargi D., Voss, Andreas, Von Hoff, Daniel D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4322997/
https://www.ncbi.nlm.nih.gov/pubmed/25415047
_version_ 1782356474341621760
author Gatalica, Zoran
Millis, Sherri Z.
Vranic, Semir
Bender, Ryan
Basu, Gargi D.
Voss, Andreas
Von Hoff, Daniel D.
author_facet Gatalica, Zoran
Millis, Sherri Z.
Vranic, Semir
Bender, Ryan
Basu, Gargi D.
Voss, Andreas
Von Hoff, Daniel D.
author_sort Gatalica, Zoran
collection PubMed
description BACKGROUND: Cancer of unknown primary (CUP) accounts for approximately 3% of all malignancies. Despite extensive laboratory and imaging efforts, the primary site usually cannot be unequivocally confirmed, and the treatment for the most part remains empirical. Recently, identification of common cancer pathway alterations in diverse cancer lineages has offered an opportunity to provide targeted therapies for patients with CUP, irrespective of the primary site. PATIENTS AND METHODS: 1806 cancers of unknown primary were identified among more than 63,000 cases profiled at Caris Life Sciences. Multiplatform profiling of the tumor samples included immunohistochemistry, gene sequencing and in situ hybridization methods in an effort to identify changes in biomarkers that are predictive of drug responses. RESULTS: Biomarkers associated with a potential drug benefit were identified in 96% of cases. Biomarkers identified included those associated with potential benefit in nearly all classes of approved cancer drugs (cytotoxic, hormonal, targeted biological drugs). Additionally, biomarkers associated with a potential lack of benefit were identified in numerous cases, which could further refine the management of patients with CUP. CONCLUSION: Comprehensive biomarker profiling of CUP may provide additional choices in treatment of patients with these difficult to treat malignancies.
format Online
Article
Text
id pubmed-4322997
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Impact Journals LLC
record_format MEDLINE/PubMed
spelling pubmed-43229972015-02-10 Comprehensive tumor profiling identifies numerous biomarkers of drug response in cancers of unknown primary site: Analysis of 1806 cases Gatalica, Zoran Millis, Sherri Z. Vranic, Semir Bender, Ryan Basu, Gargi D. Voss, Andreas Von Hoff, Daniel D. Oncotarget Clinical Research Paper BACKGROUND: Cancer of unknown primary (CUP) accounts for approximately 3% of all malignancies. Despite extensive laboratory and imaging efforts, the primary site usually cannot be unequivocally confirmed, and the treatment for the most part remains empirical. Recently, identification of common cancer pathway alterations in diverse cancer lineages has offered an opportunity to provide targeted therapies for patients with CUP, irrespective of the primary site. PATIENTS AND METHODS: 1806 cancers of unknown primary were identified among more than 63,000 cases profiled at Caris Life Sciences. Multiplatform profiling of the tumor samples included immunohistochemistry, gene sequencing and in situ hybridization methods in an effort to identify changes in biomarkers that are predictive of drug responses. RESULTS: Biomarkers associated with a potential drug benefit were identified in 96% of cases. Biomarkers identified included those associated with potential benefit in nearly all classes of approved cancer drugs (cytotoxic, hormonal, targeted biological drugs). Additionally, biomarkers associated with a potential lack of benefit were identified in numerous cases, which could further refine the management of patients with CUP. CONCLUSION: Comprehensive biomarker profiling of CUP may provide additional choices in treatment of patients with these difficult to treat malignancies. Impact Journals LLC 2014-10-31 /pmc/articles/PMC4322997/ /pubmed/25415047 Text en Copyright: © 2014 Gatalica et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
spellingShingle Clinical Research Paper
Gatalica, Zoran
Millis, Sherri Z.
Vranic, Semir
Bender, Ryan
Basu, Gargi D.
Voss, Andreas
Von Hoff, Daniel D.
Comprehensive tumor profiling identifies numerous biomarkers of drug response in cancers of unknown primary site: Analysis of 1806 cases
title Comprehensive tumor profiling identifies numerous biomarkers of drug response in cancers of unknown primary site: Analysis of 1806 cases
title_full Comprehensive tumor profiling identifies numerous biomarkers of drug response in cancers of unknown primary site: Analysis of 1806 cases
title_fullStr Comprehensive tumor profiling identifies numerous biomarkers of drug response in cancers of unknown primary site: Analysis of 1806 cases
title_full_unstemmed Comprehensive tumor profiling identifies numerous biomarkers of drug response in cancers of unknown primary site: Analysis of 1806 cases
title_short Comprehensive tumor profiling identifies numerous biomarkers of drug response in cancers of unknown primary site: Analysis of 1806 cases
title_sort comprehensive tumor profiling identifies numerous biomarkers of drug response in cancers of unknown primary site: analysis of 1806 cases
topic Clinical Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4322997/
https://www.ncbi.nlm.nih.gov/pubmed/25415047
work_keys_str_mv AT gatalicazoran comprehensivetumorprofilingidentifiesnumerousbiomarkersofdrugresponseincancersofunknownprimarysiteanalysisof1806cases
AT millissherriz comprehensivetumorprofilingidentifiesnumerousbiomarkersofdrugresponseincancersofunknownprimarysiteanalysisof1806cases
AT vranicsemir comprehensivetumorprofilingidentifiesnumerousbiomarkersofdrugresponseincancersofunknownprimarysiteanalysisof1806cases
AT benderryan comprehensivetumorprofilingidentifiesnumerousbiomarkersofdrugresponseincancersofunknownprimarysiteanalysisof1806cases
AT basugargid comprehensivetumorprofilingidentifiesnumerousbiomarkersofdrugresponseincancersofunknownprimarysiteanalysisof1806cases
AT vossandreas comprehensivetumorprofilingidentifiesnumerousbiomarkersofdrugresponseincancersofunknownprimarysiteanalysisof1806cases
AT vonhoffdanield comprehensivetumorprofilingidentifiesnumerousbiomarkersofdrugresponseincancersofunknownprimarysiteanalysisof1806cases