Quantitative mRNA Expression Assays and Synchronous Breast Cancers: A Case Report

Quantitative mRNA analysis of breast tumors represents a routinely applied example of precision oncology. Currently the National Comprehensive Cancer Network (NCCN) recommends quantitative mRNA profiling (e.g., 21-gene RT PCR or Oncotype Dx assay) for nearly all surgically resected lymph node (LN) n...

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Main Author: Steven Sorscher
Format: Article
Language:English
Published: Karger Publishers 2019-06-01
Series:Case Reports in Oncology
Subjects:
Online Access:https://www.karger.com/Article/FullText/500670
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spelling doaj-186d02c15db946ed8cbef652384fe7312020-11-25T00:17:51ZengKarger PublishersCase Reports in Oncology1662-65752019-06-0112241842010.1159/000500670500670Quantitative mRNA Expression Assays and Synchronous Breast Cancers: A Case ReportSteven SorscherQuantitative mRNA analysis of breast tumors represents a routinely applied example of precision oncology. Currently the National Comprehensive Cancer Network (NCCN) recommends quantitative mRNA profiling (e.g., 21-gene RT PCR or Oncotype Dx assay) for nearly all surgically resected lymph node (LN) negative hormone receptor (HR) positive, HER2 negative breast cancers in order to predict recurrence risk with endocrine therapy compared to chemotherapy followed by endocrine therapy after surgery. The incidence of synchronous breast cancers is low and evidence concerning distant recurrence risk is limited, but the risk of distant recurrence from one or the other of two primary breast cancers appears to be higher than the recurrence risk of the single largest of the two cancers. In this report, a woman with synchronous primary breast cancers is described. Oncotype Dx testing was done on each of her two cancers. By assuming that the recurrence risk from each with adjuvant endocrine therapy is an independent event, the recurrence likelihood from one or the other or both is calculated. I propose that this calculated value more accurately should predict the recurrence from one or the other or both tumors with endocrine therapy or chemotherapy followed by endocrine therapy compared with using only the higher of the two Oncotype Dx estimated risks.https://www.karger.com/Article/FullText/500670SynchronousRisk assessmentQuantitative RNA
collection DOAJ
language English
format Article
sources DOAJ
author Steven Sorscher
spellingShingle Steven Sorscher
Quantitative mRNA Expression Assays and Synchronous Breast Cancers: A Case Report
Case Reports in Oncology
Synchronous
Risk assessment
Quantitative RNA
author_facet Steven Sorscher
author_sort Steven Sorscher
title Quantitative mRNA Expression Assays and Synchronous Breast Cancers: A Case Report
title_short Quantitative mRNA Expression Assays and Synchronous Breast Cancers: A Case Report
title_full Quantitative mRNA Expression Assays and Synchronous Breast Cancers: A Case Report
title_fullStr Quantitative mRNA Expression Assays and Synchronous Breast Cancers: A Case Report
title_full_unstemmed Quantitative mRNA Expression Assays and Synchronous Breast Cancers: A Case Report
title_sort quantitative mrna expression assays and synchronous breast cancers: a case report
publisher Karger Publishers
series Case Reports in Oncology
issn 1662-6575
publishDate 2019-06-01
description Quantitative mRNA analysis of breast tumors represents a routinely applied example of precision oncology. Currently the National Comprehensive Cancer Network (NCCN) recommends quantitative mRNA profiling (e.g., 21-gene RT PCR or Oncotype Dx assay) for nearly all surgically resected lymph node (LN) negative hormone receptor (HR) positive, HER2 negative breast cancers in order to predict recurrence risk with endocrine therapy compared to chemotherapy followed by endocrine therapy after surgery. The incidence of synchronous breast cancers is low and evidence concerning distant recurrence risk is limited, but the risk of distant recurrence from one or the other of two primary breast cancers appears to be higher than the recurrence risk of the single largest of the two cancers. In this report, a woman with synchronous primary breast cancers is described. Oncotype Dx testing was done on each of her two cancers. By assuming that the recurrence risk from each with adjuvant endocrine therapy is an independent event, the recurrence likelihood from one or the other or both is calculated. I propose that this calculated value more accurately should predict the recurrence from one or the other or both tumors with endocrine therapy or chemotherapy followed by endocrine therapy compared with using only the higher of the two Oncotype Dx estimated risks.
topic Synchronous
Risk assessment
Quantitative RNA
url https://www.karger.com/Article/FullText/500670
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