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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...

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Autores principales: Arend, Rebecca C., Scalise, Carly B., Dholakia, Jhalak, Kamal, Maahum Z., Thigpen, Haley B., Crossman, David, Huh, Warner K., Leath, Charles A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
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.
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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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