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Performance and prognostic utility of the 92-gene assay in the molecular subclassification of ampullary adenocarcinoma

BACKGROUND: Ampullary adenocarcinoma is a rare gastrointestinal cancer associated with diverse outcomes due to clinical and pathological heterogeneity. Standardized methods to better prognosticate and inform therapeutic selection for ampullary adenocarcinoma are needed. This study explored the novel...

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Autores principales: Overman, Michael J., Soifer, Harris S., Schueneman, Aaron Joel, Ensor, Joe, Adsay, Volkan, Saka, Burcu, Neishaboori, Nastaran, Wolff, Robert A., Wang, Huamin, Schnabel, Catherine A., Varadhachary, Gauri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4994309/
https://www.ncbi.nlm.nih.gov/pubmed/27549176
http://dx.doi.org/10.1186/s12885-016-2677-3
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author Overman, Michael J.
Soifer, Harris S.
Schueneman, Aaron Joel
Ensor, Joe
Adsay, Volkan
Saka, Burcu
Neishaboori, Nastaran
Wolff, Robert A.
Wang, Huamin
Schnabel, Catherine A.
Varadhachary, Gauri
author_facet Overman, Michael J.
Soifer, Harris S.
Schueneman, Aaron Joel
Ensor, Joe
Adsay, Volkan
Saka, Burcu
Neishaboori, Nastaran
Wolff, Robert A.
Wang, Huamin
Schnabel, Catherine A.
Varadhachary, Gauri
author_sort Overman, Michael J.
collection PubMed
description BACKGROUND: Ampullary adenocarcinoma is a rare gastrointestinal cancer associated with diverse outcomes due to clinical and pathological heterogeneity. Standardized methods to better prognosticate and inform therapeutic selection for ampullary adenocarcinoma are needed. This study explored the novel use and potential prognostic utility of a 92-gene cancer classifier in ampullary adenocarcinomas. METHODS: In this prospectively-defined, blinded study of ampullary adenocarcinoma [N =54; stage T3 or higher (57 %); Grade III (44 %); Node positive (55 %)], the performance of a 92-gene classifier was examined to predict the ampullary subtype that was derived from histomorphological examination of resected ampullary samples. Outcome data for relapse-free survival (RFS) and overall survival (OS) were plotted to compare the prognostic utility of histological subtyping, histomolecular phenotyping, and the 92-gene classifier. Multivariate analysis was used to determine clinicopathological variables that were independently associated with overall survival. RESULTS: The 92-gene classifier demonstrated sensitivities and specificities of 85 % [95 % CI, 66–94] and 68 % [95 % CI, 48–84] and 64 % [95 % CI, 46–79] and 88 % [95 % CI, 70–98] for the pancreaticobiliary and intestinal histological subtypes, respectively. For the 92-gene classifier, improved outcomes were observed for the intestine versus the pancreaticobiliary prediction (median OS 108.1 v 36.4 months; HR, 2.17; 95 % CI, 0.98 to 4.79; P = 0.05). Similar results were seen for ampullary adenocarcinoma stratification by histological subtype (P = 0.04) and histomolecular phenotype (P = 0.02). Within poorly differentiated ampullary adenocarcinomas only the 92-gene classifier demonstrated statistically significant differences in RFS and OS (P < 0.05). CONCLUSIONS: Prognostic stratification of ampullary adenocarcinoma was similar for the 92-gene classifier, histological subtype, and histomolecular phenotype. The 92-gene classifier provides an unbiased standardized molecular-based approach to stratify ampullary tumors. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12885-016-2677-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-49943092016-08-24 Performance and prognostic utility of the 92-gene assay in the molecular subclassification of ampullary adenocarcinoma Overman, Michael J. Soifer, Harris S. Schueneman, Aaron Joel Ensor, Joe Adsay, Volkan Saka, Burcu Neishaboori, Nastaran Wolff, Robert A. Wang, Huamin Schnabel, Catherine A. Varadhachary, Gauri BMC Cancer Research Article BACKGROUND: Ampullary adenocarcinoma is a rare gastrointestinal cancer associated with diverse outcomes due to clinical and pathological heterogeneity. Standardized methods to better prognosticate and inform therapeutic selection for ampullary adenocarcinoma are needed. This study explored the novel use and potential prognostic utility of a 92-gene cancer classifier in ampullary adenocarcinomas. METHODS: In this prospectively-defined, blinded study of ampullary adenocarcinoma [N =54; stage T3 or higher (57 %); Grade III (44 %); Node positive (55 %)], the performance of a 92-gene classifier was examined to predict the ampullary subtype that was derived from histomorphological examination of resected ampullary samples. Outcome data for relapse-free survival (RFS) and overall survival (OS) were plotted to compare the prognostic utility of histological subtyping, histomolecular phenotyping, and the 92-gene classifier. Multivariate analysis was used to determine clinicopathological variables that were independently associated with overall survival. RESULTS: The 92-gene classifier demonstrated sensitivities and specificities of 85 % [95 % CI, 66–94] and 68 % [95 % CI, 48–84] and 64 % [95 % CI, 46–79] and 88 % [95 % CI, 70–98] for the pancreaticobiliary and intestinal histological subtypes, respectively. For the 92-gene classifier, improved outcomes were observed for the intestine versus the pancreaticobiliary prediction (median OS 108.1 v 36.4 months; HR, 2.17; 95 % CI, 0.98 to 4.79; P = 0.05). Similar results were seen for ampullary adenocarcinoma stratification by histological subtype (P = 0.04) and histomolecular phenotype (P = 0.02). Within poorly differentiated ampullary adenocarcinomas only the 92-gene classifier demonstrated statistically significant differences in RFS and OS (P < 0.05). CONCLUSIONS: Prognostic stratification of ampullary adenocarcinoma was similar for the 92-gene classifier, histological subtype, and histomolecular phenotype. The 92-gene classifier provides an unbiased standardized molecular-based approach to stratify ampullary tumors. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12885-016-2677-3) contains supplementary material, which is available to authorized users. BioMed Central 2016-08-22 /pmc/articles/PMC4994309/ /pubmed/27549176 http://dx.doi.org/10.1186/s12885-016-2677-3 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Overman, Michael J.
Soifer, Harris S.
Schueneman, Aaron Joel
Ensor, Joe
Adsay, Volkan
Saka, Burcu
Neishaboori, Nastaran
Wolff, Robert A.
Wang, Huamin
Schnabel, Catherine A.
Varadhachary, Gauri
Performance and prognostic utility of the 92-gene assay in the molecular subclassification of ampullary adenocarcinoma
title Performance and prognostic utility of the 92-gene assay in the molecular subclassification of ampullary adenocarcinoma
title_full Performance and prognostic utility of the 92-gene assay in the molecular subclassification of ampullary adenocarcinoma
title_fullStr Performance and prognostic utility of the 92-gene assay in the molecular subclassification of ampullary adenocarcinoma
title_full_unstemmed Performance and prognostic utility of the 92-gene assay in the molecular subclassification of ampullary adenocarcinoma
title_short Performance and prognostic utility of the 92-gene assay in the molecular subclassification of ampullary adenocarcinoma
title_sort performance and prognostic utility of the 92-gene assay in the molecular subclassification of ampullary adenocarcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4994309/
https://www.ncbi.nlm.nih.gov/pubmed/27549176
http://dx.doi.org/10.1186/s12885-016-2677-3
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