45 Application of the 7-Gene Biosignature in Palpable Versus Nonpalpable Ductal Carcinoma In Situ in a Black Patient Population: Does Palpability Suggest a More Aggressive Genomic Risk?

Publication
Article
Miami Breast Cancer Conference® Abstracts Supplement41st Annual Miami Breast Cancer Conference® - Abstracts
Volume 38
Issue 4
Pages: 53-54

Background

Palpable ductal carcinoma in situ (p-DCIS) is a rare entity—only 10% of patients present with a clinical mass. We have noticed high rates of palpability among our African American patient population.

Previous studies have suggested that p-DCIS may be associated with more aggressive clinicohistologic features such as higher nuclear grade, comedonecrosis, HER2-neu positivity, and being hormone receptor-negative. DCISionRT (DRT) is a 7-gene biosignature that predicts recurrence risk, defined as either a low (0-3) or elevated (3.1-10) score. We hypothesized that p-DCIS cases in our African American patient population would have higher DRT scores when compared with nonpalpable cases (n-DCIS).

Methods

An institutional review board (IRB)-approved retrospective chart review was performed on all cases of DCIS identified at a single institution from 2021 to 2023. All cases had the results of the DRT scores. We analyzed clinical, histologic, and demographic features and used descriptive statistics to compare groups.

DRT Scores

DRT Scores

Results

Thirty-four patients were identified in the cohort and all self-identified as African American. Fourteen patients (41%) presented with a clinically palpable mass, while 20 (59%) were detected on imaging. Overall, 25/34 (74%) had an elevated DRT score. Nine of the 14 patients (64%) of p-DCIS cases had an elevated DRT score while 5 (36%) had low scores. Out of n-DCIS cases, 16 (80%) had elevated DRT scores while 4 (20%) had low scores (Pearson chi: 1.0448; P = .307).


Conclusion

While invasive breast cancer is known to be more aggressive among African American women, studies have failed to identify a more aggressive in situ histology in this population. Here we report a higher-than-average rate of palpability at 41%. While most of the patients in our cohort had an elevated DRT score overall, there was no significant difference when comparing both groups. Further studies are warranted to identify factors that may predict in situ or invasive recurrence in this population.

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1 Centrally Located Breast Cancer Is More Aggressive in Bahraini Patients
2 Is Laterality in Breast Cancer Still Worth Studying? Local Experience in Bahrain
2 Is Laterality in Breast Cancer Still Worth Studying? Local Experience in Bahrain
3 Gender Disparities in the  National Institutes of Health  Funding for Breast Cancer
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4 Bacopaside: Exploring Its Potential in Addressing Chemoresistance and Modulating Doxorubicin Accumulation in Triple-Negative Breast Cancer Cells
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5 Predictors of Axillary Complete Pathologic Response in Hormone Receptor–Positive, HER2-Negative, Clinically Node-Positive Breast Cancer
5 Predictors of Axillary Complete Pathologic Response in Hormone Receptor–Positive, HER2-Negative, Clinically Node-Positive Breast Cancer
6 Treatment Outcomes of the KEYNOTE-522 Regimen in an Ethnically Diverse Patient Population
6 Treatment Outcomes of the KEYNOTE-522 Regimen in an Ethnically Diverse Patient Population
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8 Using a Liquid Biopsy Mediated Approach for Determination of HER2 Amplification Status in Patient Samples
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9 Elacestrant (ELA) vs Standard-of-Care (SOC) in ER+/HER2–Advanced (adv) or Metastatic Breast Cancer (mBC) with ESR1 Mutation (ESR1-mut): Key Biomarkers and Clinical Subgroup Analyses From the Phase 3 EMERALD Trial
9 Elacestrant (ELA) vs Standard-of-Care (SOC) in ER+/HER2–Advanced (adv) or Metastatic Breast Cancer (mBC) with ESR1 Mutation (ESR1-mut): Key Biomarkers and Clinical Subgroup Analyses From the Phase 3 EMERALD Trial
10 Real-World Effectiveness of Palbociclib (PAL) Plus Aromatase Inhibitors (AI) in Patients With Metastatic Breast Cancer (MBC) and Cardiovascular Diseases (CVD)
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11 Phase 3 Study of Neoadjuvant Pembrolizumab or Placebo Plus Chemotherapy, Followed by Adjuvant Pembrolizumab or Placebo Plus Endocrine Therapy for Early-Stage High-Risk ER+/HER2– Breast Cancer: KEYNOTE-756
11 Phase 3 Study of Neoadjuvant Pembrolizumab or Placebo Plus Chemotherapy, Followed by Adjuvant Pembrolizumab or Placebo Plus Endocrine Therapy for Early-Stage High-Risk ER+/HER2– Breast Cancer: KEYNOTE-756
12 EMERALD Trial Analysis of Patient-Reported Outcomes (PROs) in Patients (pts) With ER+/HER2- Advanced or Metastatic Breast  Cancer (mBC) Comparing Oral Elacestrant vs Standard-of-Care (SoC) Endocrine Therapy
12 EMERALD Trial Analysis of Patient-Reported Outcomes (PROs) in Patients (pts) With ER+/HER2- Advanced or Metastatic Breast Cancer (mBC) Comparing Oral Elacestrant vs Standard-of-Care (SoC) Endocrine Therapy
13 The Cause and Eradication of Breast Cancer
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14 Outcomes With First-Line (1L) Ribociclib (RIB) + Endocrine Therapy (ET) vs Physician’s Choice Combination Chemotherapy (combo CT) by Age in Pre/Perimenopausal Patients (pts) With Aggressive HR+/HER2– Advanced Breast Cancer (ABC): A Subgroup Analysis of the RIGHT Choice Trial
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