63 Choice Architecture Bias in Genetic Counseling of Breast Cancer Patients

Publication
Article
Miami Breast Cancer Conference® Abstracts Supplement41st Annual Miami Breast Cancer Conference® - Abstracts
Volume 38
Issue 4
Pages: 76-77

Background

American Society of Breast Surgeons (ASBrS) consensus guidelines recommend genetic testing be available to all patients with a personal history of breast cancer, with the National Comprehensive Cancer Network allowing for multigene panel testing beyond the most common pathogenic variants of breast cancer. Genetic counseling is typically provided by breast surgeons or genetic counselors. However, there are no formal recommendations for the breadth of genes to be tested.

The ASBrS asserts genetic testing should occur in the context of informed consent. In this context, the breadth of genetic testing should be decided by the patient following pretest counseling.

Choice architecture posits that decisions are influenced by how choices are presented. Depending on the bias of the choice architect, be it surgeon or genetic counselor, there may be differences in the size of panels ordered for which there should be none.

Methods

Breast surgeons (n = 4) and genetic counselors (n = 5) with more than 50 genetic test orders among the breast cancer population within a 7-hospital system were audited over a 3-year period (n = 3912 tests). The median number of genes ordered was used to create order categories: less than median vs at least median. Chi-square analyses were used to compare the relationships between order category and clinician as well as order category and clinician’s role.

Results

Genetic Tests Ordered by Breast Surgeons and Genetic Counselors

Genetic Tests Ordered by Breast Surgeons and Genetic Counselors

The median number of genes tested was 48 (IQR, 32-85). There were significant differences in the proportion of orders above the median among the 4 breast surgeons (P < .001) as well as among the 5 genetic counselors (P < .001). In contrast, there was no difference in the proportion of orders above the median between the 2 clinician groups (P = .50).


Discussion

These data lack propensity-matching of the breast cancer populations, yet there is significant anchoring in 5 of 9 clinicians, where greater than 90% of their panels are either greater or fewer than the median. This suggests a wide variation in the pretest counseling provided among both breast surgeons and genetic counselors. The differences in ordering panels indicates further research and guidelines may be warranted in this rapidly evolving component of the care of patients with breast cancer.

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2 Is Laterality in Breast Cancer Still Worth Studying? Local Experience in Bahrain
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4 Bacopaside: Exploring Its Potential in Addressing Chemoresistance and Modulating Doxorubicin Accumulation in Triple-Negative Breast Cancer Cells
4 Bacopaside: Exploring Its Potential in Addressing Chemoresistance and Modulating Doxorubicin Accumulation in Triple-Negative Breast Cancer Cells
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
7 Real-World Efficacy and Adverse Events of Neoadjuvant Immunotherapy in Early-Stage Triple-Negative Breast Cancer Patients: A Multicenter Experience
7 Real-World Efficacy and Adverse Events of Neoadjuvant Immunotherapy in Early-Stage Triple-Negative Breast Cancer Patients: A Multicenter Experience
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)
10 Real-World Effectiveness of Palbociclib (PAL) Plus Aromatase Inhibitors (AI) in Patients With Metastatic Breast Cancer (MBC) and Cardiovascular Diseases (CVD)
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
13 The Cause and Eradication of Breast Cancer
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
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
15 Concurrent Use of Abemaciclib and Radiation Therapy (RT) Among Patients With HR+, HER2– Metastatic Breast Cancer (MBC): Real-World Utilization and Safety
15 Concurrent Use of Abemaciclib and Radiation Therapy (RT) Among Patients With HR+, HER2– Metastatic Breast Cancer (MBC): Real-World Utilization and Safety
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