Exact Sciences Presents Multiple Studies At San Antonio Breast Cancer Symposium Supporting Optimization And Individualization Of Therapy For Breast Cancer Patients

1.

Title:
Magnetic Resonance Imaging and a 12-Gene Expression Assay to Optimize Local Therapy for Ductal Carcinoma In Situ: 5-year clinical outcomes of E4112 -
Chosen for SABCS Press Program

Summary: This prospective trial, the first to evaluate the predictive ability of the 12-gene DCIS score, provides data regarding the omission of radiation therapy after surgery in patients with DCIS breast cancer who have low DCIS score results, and the benefit of radiation therapy in patients with intermediate/high DS results.

Oral Presentation ID:
GS03-01: Friday, December 8, 2023, 8:15-11:15 a.m.

2.

Title: Impact of age and ovarian function suppression (OFS) on endocrine response to short preoperative endocrine therapy (ET): Results from the
multicenter ADAPTcycle trial Chosen as Late Breaking Abstract at SABCS

Data embargoed until:
7:15 a.m. CT on Friday, December 8

Presentation ID:
LBO1-05: Friday, December 8, 2023, 12:00-12:45 p.m.

3.

Title:
Comparison of whole exome, whole transcriptome genomic profiling and targeted sequencing with 50-gene panels

Summary:
A comparison of the OncoExTraTM whole-exome, whole-transcriptome, comprehensive genomic profiling test to three commercially available and one custom 50-gene panels in a cohort of breast cancer patients. The study determined the frequency of patient tumors that would have had no actionable alteration identified when employing each of the 50-gene panels, when an actionable alteration identified by the OncoExTra test was present, across the three different breast cancer subtypes. The highest proportion of patients was missed (no actionable finding) by 50-gene panels when the cancer was the TNBC subtype and the lowest for HER2+.

Presentation ID:
Poster ID PO5-13-05: Friday, December 8, 2023, 12:00-2:00 p.m. (Poster Session 5)

4.

Title: Classifying HER2-low breast cancer using a combination of ERBB2 mRNA expression and altered genes

Summary: Comparison of ERBB2 gene expression, measured using mRNA levels, with HER2 (encoded by ERBB2 gene) protein expression, measured by IHC/FISH. A comparison of altered biomarkers across HER2 protein expression categories was also made. ERBB2 expression levels and alterations in selected biomarkers were used to train a logistic regression classifier to predict HER2 protein expression status. Preliminary results indicate that some HER2-0 samples were classified as HER2-low by the classifier.

Presentation ID:
Poster ID P05-13-06: Friday December 8, 2023, 12:00 -2:00 p.m. (Poster Session 5)

5.

Title:
Prevalence of genomic alterations in Xerna tumor microenvironment subtypes in triple negative breast cancer patients

Summary:
203 triple negative breast cancer tumor samples were assigned to four different Xerna tumor-microenvironment categories (high versus low immune score, high versus low angiogenic score) based on gene expression of about 100 genes. The prevalence of actionable alterations in biomarkers was then determined across these four tumor microenvironment subtypes. About half of cancer samples had high immune scores, suggesting possible response to ICI therapy. More than half of patient samples carried actionable alterations. Together, these findings suggest the possibility of novel combination therapies in some TNBC patients.

Presentation ID:
Poster ID PO2-06-10: Wednesday Dec 6, 2023, 5:00-7:00 p.m. (Poster Session 2)

6.

Title: Hereditary cancer genetic testing in Puerto Rican females

Summary:
Nearly one thousand Puerto Rican females were tested with a hereditary cancer panel containing 29 genes. 90 (9.5%) individuals had a pathogenic or likely pathogenic alteration in their germ line at one or more of these genes. The proportion of individuals carrying a pathogenic/likely pathogenic variant at a cancer gene is within the range reported for other Caribbean countries. However, there was no evidence for enrichment of alterations at BRCA1, BRCA2 and PALB2 as observed in other Caribbean countries. The study also denotes a lack of genetic testing amongst specific disparate populations.

Presentation ID:
Poster ID :
PO1-08-08: Wednesday, December 6, 2023, 12:00 p.m.-2:00 p.m. (Poster Session 1)

7.

Title:
Concordance Study of Oncotype DX Breast Recurrence Score® Results from Paired Breast Cancer Core Needle Biopsies and Surgical Excision Specimens

Summary:
Comparison of Oncotype DX Recurrence Score results for paired core needle biopsy and surgical samples of the same tumor without intervening systemic therapy, which found high concordance between the two.

Presentation ID: PO4-08-09: Thursday, December 7, 2023, 5:00-7:00 p.m. (Poster Session 4)

8.

Title:
Comparison of the cost-effectiveness of multigene assays for HR+/HER2- node-negative early-stage breast cancer in the US

Summary:
Compares the cost-effectiveness of using different genomic assays for treatment decisions in HR+HER2- early breast cancer (Oncotype DX, MammaPrint, EndoPredict, and Prosigna ROR) relative to that of using clinical-pathological features alone in the U.S. The modeling found that all were cost-effective as additions to clinical-pathological features, with the Oncotype DX test providing the greatest cost savings among the four.

Presentation ID:
PO1-01-10:
Wednesday, December 6, 2023, 12:00 -2:00 p.m. (Poster Session 1)

9.

Title:
A comparison of chemotherapy recommendations by NPI, Predict, and Oncotype DX testing in UK women with early node-positive breast cancer

Summary:
Comparison of the Oncotype DX Recurrence Score test, the Nottingham Prognostic Index, and the Predict Breast Cancer tool in risk stratification and association with chemotherapy recommendations in HR+HER2- node-positive early breast cancer. Of the three, the Oncotype test was the most strongly associated with chemotherapy recommendation.

Presentation ID:
PO1-14-05: Wednesday, December 6, 2023, 12:00-2:00 p.m. (Poster Session 1)

10.

Title:
Update of RSClin tool with extended TAILORx follow-up and development and validation of a new tool for risk of late distant recurrence

Summary:
Update of the TAILORx findings with longer follow-up and resulting refinements to the RSClin tool for estimating 10-year risk of distant recurrence in HR+HER2- early breast cancer. A new tool specifically to estimate late (5-10 year) distant recurrence risk is also presented.

Presentation ID:
PO1-02-02: Wednesday, December 6, 2023, 12:00-2:00 p.m. (Poster Session 1)

11.

Title : Irish National Analysis of the Clinical and Economic impact of 21-gene Oncotype DX® testing in Early-Stage, 1-3 lymph node-positive,
Hormone Receptor positive (HR+), HER2-Negative (HER2-), Breast Cancer (BC)

Summary: An analysis of the impact of Oncotype DX® testing in a N1 (disease with 1-3 positive LN) breast cancer population from 2 Irish cancer centers identified a 55% reduction in chemotherapy use with savings of over €1 million. The objectives of this study were to examine the clinical and economic impact of Oncotype DX testing on treatment decisions in N1 patients at a national level with a larger patient population, and to examine changes in the ordering of Oncotype DX tests pre- and post-RxPONDER data. This study extended the analysis to 5 Irish cancer centers.

Presentation ID:
PO5-02-04: Friday, December 8, 2023, 12:00-2:00 p.m. (Poster Session 5)

12.

Title: Real-world application of a 21-gene recurrence score in a Swiss single center breast cancer population. A comparative analysis of treatment administration before and after
TAILORx

Summary:
A comparison of chemotherapy recommendations and use before and after TAILORx.
There were some differences in treatment recommendations after
TAILORx that included increased recommendation for addition of chemotherapy to endocrine therapy, specifically among younger women, but there were no significant changes in chemotherapy administration.

Presentation ID: Poster Number: P1-14-02: Wednesday December 6, 2023, 12:00-2:00 p.m. (Poster Session 1)

Media (U.S.):

Media (OUS):

Investors:

Jack Hirschfield

Federico Maiardi

Erik Holznecht

+1 608-852-9877

+41 79-138-1326

+1 608-852-9877

[email protected]

[email protected]

[email protected]