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Updated: Jan 22, 2026

Optimization of a Multiplex RNA-based Expression Assay Using Breast Cancer Archival Material
Published on: August 1, 2018
Quantitative mRNA Expression Assays and Synchronous Breast Cancers: A Case Report
1Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
Abstract:
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.
Insights
For patients with synchronous breast cancers, calculating combined recurrence risk from Oncotype Dx assays provides a more accurate prediction than using the highest individual risk score. This approach aids precision oncology treatment decisions.
Area of Science:
- Oncology
- Genomics
- Precision Medicine
Background:
- National Comprehensive Cancer Network (NCCN) guidelines recommend quantitative mRNA profiling for early-stage, hormone receptor-positive, HER2-negative breast cancers to guide adjuvant therapy decisions.
- Quantitative mRNA assays like the 21-gene RT-PCR (Oncotype Dx) predict recurrence risk and response to endocrine therapy versus chemotherapy.
Observation:
- Synchronous primary breast cancers are rare, with limited data on their combined distant recurrence risk.
- The recurrence risk from two primary breast cancers may exceed the risk from the larger single tumor.
Findings:
- This report details a case of synchronous primary breast cancers where Oncotype Dx was performed on both tumors.
- A novel calculation method was used to estimate the combined recurrence risk, treating each tumor's risk as an independent event.
- The proposed calculation method aims to provide a more accurate prediction of recurrence risk compared to using the higher of the two individual Oncotype Dx scores.
Implications:
- This approach may improve risk stratification for patients with multiple primary breast cancers.
- Accurate recurrence risk assessment is crucial for optimizing adjuvant endocrine therapy and chemotherapy decisions in precision oncology.
- Further research is needed to validate this combined risk calculation method in a larger cohort of patients with synchronous breast cancers.
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