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EGFR as a prognostic biomarker and therapeutic target in ovarian cancer: evaluation of patient cohort and literature review

BACKGROUND: Limited effectiveness of therapeutic agents targeting epidermal growth factor receptor (EGFR) in clinical trials using unselected ovarian cancer patients has prompted efforts to more effectively stratify patients who might best benefit from these therapies. A series of studies that have...

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Autores principales: Mehner, Christine, Oberg, Ann L., Goergen, Krista M., Kalli, Kimberly R., Maurer, Matthew J., Nassar, Aziza, Goode, Ellen L., Keeney, Gary L., Jatoi, Aminah, Radisky, Derek C., Radisky, Evette S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5511892/
https://www.ncbi.nlm.nih.gov/pubmed/28740577
http://dx.doi.org/10.18632/genesandcancer.142
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author Mehner, Christine
Oberg, Ann L.
Goergen, Krista M.
Kalli, Kimberly R.
Maurer, Matthew J.
Nassar, Aziza
Goode, Ellen L.
Keeney, Gary L.
Jatoi, Aminah
Radisky, Derek C.
Radisky, Evette S.
author_facet Mehner, Christine
Oberg, Ann L.
Goergen, Krista M.
Kalli, Kimberly R.
Maurer, Matthew J.
Nassar, Aziza
Goode, Ellen L.
Keeney, Gary L.
Jatoi, Aminah
Radisky, Derek C.
Radisky, Evette S.
author_sort Mehner, Christine
collection PubMed
description BACKGROUND: Limited effectiveness of therapeutic agents targeting epidermal growth factor receptor (EGFR) in clinical trials using unselected ovarian cancer patients has prompted efforts to more effectively stratify patients who might best benefit from these therapies. A series of studies that have evaluated immunohistochemical (IHC) staining of EGFR in ovarian cancer biopsies has produced unclear results as to the utility of this measure as a prognostic biomarker. Here, we used one of the largest, single institution cohorts to date to determine possible associations of EGFR expression with patient outcome. METHODS: We performed IHC staining of EGFR in tissue microarrays including nearly 500 patient tumor samples. Staining was classified by subcellular localization (membranous, cytoplasmic) or by automated image analysis algorithms. We also performed a literature review to place these results in the context of previous studies. RESULTS: No significant associations were found between EGFR subcellular localization or expression and histology, stage, grade, or outcome. These results were broadly consistent with the consensus of the reviewed literature. CONCLUSIONS: These results suggest that IHC staining for EGFR may not be a useful prognostic biomarker for ovarian cancer patients. Future studies should pursue other staining methods or analysis in combination with other pathway mediators.
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spelling pubmed-55118922017-07-24 EGFR as a prognostic biomarker and therapeutic target in ovarian cancer: evaluation of patient cohort and literature review Mehner, Christine Oberg, Ann L. Goergen, Krista M. Kalli, Kimberly R. Maurer, Matthew J. Nassar, Aziza Goode, Ellen L. Keeney, Gary L. Jatoi, Aminah Radisky, Derek C. Radisky, Evette S. Genes Cancer Research Paper BACKGROUND: Limited effectiveness of therapeutic agents targeting epidermal growth factor receptor (EGFR) in clinical trials using unselected ovarian cancer patients has prompted efforts to more effectively stratify patients who might best benefit from these therapies. A series of studies that have evaluated immunohistochemical (IHC) staining of EGFR in ovarian cancer biopsies has produced unclear results as to the utility of this measure as a prognostic biomarker. Here, we used one of the largest, single institution cohorts to date to determine possible associations of EGFR expression with patient outcome. METHODS: We performed IHC staining of EGFR in tissue microarrays including nearly 500 patient tumor samples. Staining was classified by subcellular localization (membranous, cytoplasmic) or by automated image analysis algorithms. We also performed a literature review to place these results in the context of previous studies. RESULTS: No significant associations were found between EGFR subcellular localization or expression and histology, stage, grade, or outcome. These results were broadly consistent with the consensus of the reviewed literature. CONCLUSIONS: These results suggest that IHC staining for EGFR may not be a useful prognostic biomarker for ovarian cancer patients. Future studies should pursue other staining methods or analysis in combination with other pathway mediators. Impact Journals LLC 2017-05 /pmc/articles/PMC5511892/ /pubmed/28740577 http://dx.doi.org/10.18632/genesandcancer.142 Text en Copyright: © 2017 Mehner et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Research Paper
Mehner, Christine
Oberg, Ann L.
Goergen, Krista M.
Kalli, Kimberly R.
Maurer, Matthew J.
Nassar, Aziza
Goode, Ellen L.
Keeney, Gary L.
Jatoi, Aminah
Radisky, Derek C.
Radisky, Evette S.
EGFR as a prognostic biomarker and therapeutic target in ovarian cancer: evaluation of patient cohort and literature review
title EGFR as a prognostic biomarker and therapeutic target in ovarian cancer: evaluation of patient cohort and literature review
title_full EGFR as a prognostic biomarker and therapeutic target in ovarian cancer: evaluation of patient cohort and literature review
title_fullStr EGFR as a prognostic biomarker and therapeutic target in ovarian cancer: evaluation of patient cohort and literature review
title_full_unstemmed EGFR as a prognostic biomarker and therapeutic target in ovarian cancer: evaluation of patient cohort and literature review
title_short EGFR as a prognostic biomarker and therapeutic target in ovarian cancer: evaluation of patient cohort and literature review
title_sort egfr as a prognostic biomarker and therapeutic target in ovarian cancer: evaluation of patient cohort and literature review
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5511892/
https://www.ncbi.nlm.nih.gov/pubmed/28740577
http://dx.doi.org/10.18632/genesandcancer.142
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