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Identifying a molecular profile to predict the risk of recurrence in high‐intermediate risk endometrial cancer
BACKGROUND: Patients with high‐intermediate risk endometrial cancer (H‐IR EMCA) have an elevated risk of recurrence compared to low‐risk counterparts. Many H‐IR EMCA patients are treated with radiation or chemotherapy, but their overall survival is not significantly impacted by treatment. The object...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8607249/ https://www.ncbi.nlm.nih.gov/pubmed/34729947 http://dx.doi.org/10.1002/cam4.4247 |
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author | Arend, Rebecca C. Scalise, Carly B. Dholakia, Jhalak Kamal, Maahum Z. Thigpen, Haley B. Crossman, David Huh, Warner K. Leath, Charles A. |
author_facet | Arend, Rebecca C. Scalise, Carly B. Dholakia, Jhalak Kamal, Maahum Z. Thigpen, Haley B. Crossman, David Huh, Warner K. Leath, Charles A. |
author_sort | Arend, Rebecca C. |
collection | PubMed |
description | BACKGROUND: Patients with high‐intermediate risk endometrial cancer (H‐IR EMCA) have an elevated risk of recurrence compared to low‐risk counterparts. Many H‐IR EMCA patients are treated with radiation or chemotherapy, but their overall survival is not significantly impacted by treatment. The objective of this study was to compare molecular profiles of H‐IR EMCA patients with disease recurrence to those without to identify characteristics that could better predict patient outcomes. METHODS: Tissue was acquired from H‐IR EMCA patients with disease recurrence (n=15) and without disease recurrence (n=15) who had not received adjuvant therapy and performed DNA and RNA analyses. RESULTS: In recurrent population, 5 patients had matchingrecurrent and initial tumor tissues. Of note, 5/7 (71%) African Americanpatients had disease recurrence compared to 10/23 (43%) White patients. Inaddition, several new mutations were found in individual patient’s recurrentcompared to initial tumors. CONCLUSIONS: Currently the treatment ofendometrial cancer is rapidly changing with molecular profiling becoming partof the standard of care. Additionally, it and is being incorporated intoclinical trials in this group of patients. The specific gene mutations and RNAexpression signatures that were observed in our small cohort need to bevalidated in larger cohorts to determine their impact. |
format | Online Article Text |
id | pubmed-8607249 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-86072492021-11-29 Identifying a molecular profile to predict the risk of recurrence in high‐intermediate risk endometrial cancer Arend, Rebecca C. Scalise, Carly B. Dholakia, Jhalak Kamal, Maahum Z. Thigpen, Haley B. Crossman, David Huh, Warner K. Leath, Charles A. Cancer Med Bioinfomatics BACKGROUND: Patients with high‐intermediate risk endometrial cancer (H‐IR EMCA) have an elevated risk of recurrence compared to low‐risk counterparts. Many H‐IR EMCA patients are treated with radiation or chemotherapy, but their overall survival is not significantly impacted by treatment. The objective of this study was to compare molecular profiles of H‐IR EMCA patients with disease recurrence to those without to identify characteristics that could better predict patient outcomes. METHODS: Tissue was acquired from H‐IR EMCA patients with disease recurrence (n=15) and without disease recurrence (n=15) who had not received adjuvant therapy and performed DNA and RNA analyses. RESULTS: In recurrent population, 5 patients had matchingrecurrent and initial tumor tissues. Of note, 5/7 (71%) African Americanpatients had disease recurrence compared to 10/23 (43%) White patients. Inaddition, several new mutations were found in individual patient’s recurrentcompared to initial tumors. CONCLUSIONS: Currently the treatment ofendometrial cancer is rapidly changing with molecular profiling becoming partof the standard of care. Additionally, it and is being incorporated intoclinical trials in this group of patients. The specific gene mutations and RNAexpression signatures that were observed in our small cohort need to bevalidated in larger cohorts to determine their impact. John Wiley and Sons Inc. 2021-11-02 /pmc/articles/PMC8607249/ /pubmed/34729947 http://dx.doi.org/10.1002/cam4.4247 Text en © 2021 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Bioinfomatics Arend, Rebecca C. Scalise, Carly B. Dholakia, Jhalak Kamal, Maahum Z. Thigpen, Haley B. Crossman, David Huh, Warner K. Leath, Charles A. Identifying a molecular profile to predict the risk of recurrence in high‐intermediate risk endometrial cancer |
title | Identifying a molecular profile to predict the risk of recurrence in high‐intermediate risk endometrial cancer |
title_full | Identifying a molecular profile to predict the risk of recurrence in high‐intermediate risk endometrial cancer |
title_fullStr | Identifying a molecular profile to predict the risk of recurrence in high‐intermediate risk endometrial cancer |
title_full_unstemmed | Identifying a molecular profile to predict the risk of recurrence in high‐intermediate risk endometrial cancer |
title_short | Identifying a molecular profile to predict the risk of recurrence in high‐intermediate risk endometrial cancer |
title_sort | identifying a molecular profile to predict the risk of recurrence in high‐intermediate risk endometrial cancer |
topic | Bioinfomatics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8607249/ https://www.ncbi.nlm.nih.gov/pubmed/34729947 http://dx.doi.org/10.1002/cam4.4247 |
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