Genomics of ERBB2-Positive Breast Cancer in Young Women Before and After Exposure to Chemotherapy Plus Trastuzumab

Author:

Lipsyc-Sharf Marla123ORCID,Jain Esha456,Collins Laura C.37,Rosenberg Shoshana M.8ORCID,Ruddy Kathryn J.9ORCID,Tamimi Rulla M.810,Schapira Lidia11ORCID,Come Steven E.312ORCID,Peppercorn Jeffrey M.313ORCID,Borges Virginia F.14ORCID,Warner Ellen15,Snow Craig12,Krop Ian E.1216ORCID,Kim Dewey5,Weiss Jakob5ORCID,Zanudo Jorge Gomez Tejeda135ORCID,Partridge Ann H.123ORCID,Wagle Nikhil123ORCID,Waks Adrienne G.123ORCID

Affiliation:

1. Medical Oncology, Dana-Farber Cancer Institute, Boston, MA

2. Breast Oncology Program, Dana-Farber Brigham Cancer Center, Boston, MA

3. Harvard Medical School, Boston, MA

4. Dana-Farber Cancer Institute, Boston, MA

5. Broad Institute of MIT and Harvard, Cambridge, MA

6. Repare Therapeutics, Cambridge, MA

7. Beth Israel Deaconess Medical Center, Boston, MA

8. Weill Cornell Medicine, New York, NY

9. Department of Oncology, Mayo Clinic, Rochester, MN

10. Brigham and Women's Hospital, Boston, MA

11. Stanford Cancer Institute, Palo Alto, CA

12. Breast Medical Oncology Program, Beth Israel Deaconess Medical Center and Dana-Farber/Harvard Cancer Center, Boston, MA

13. Massachusetts General Hospital, Boston, MA

14. University of Colorado Anschutz Medical Center, Aurora, CO

15. Odette Cancer Centre, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada

16. Yale Cancer Center, New Haven, CT

Abstract

PURPOSE Erb-B2 receptor tyrosine kinase 2 ( ERBB2)–positive breast cancer (BC) is particularly common in young women. Genomic features of ERBB2-positive tumors before and after chemotherapy and trastuzumab (chemo + H) have not been described in young women and are important for guiding study of therapeutic resistance in this population. METHODS From a large prospective cohort of women age 40 years or younger with BC, we identified patients with ERBB2-positive BC and tumor tissue available before and after chemo + H. Whole-exome sequencing (WES) was performed on each tumor and on germline DNA from blood. Tumor-normal pairs were analyzed for mutations and copy number (CN) changes. RESULTS Twenty-two women had successful WES on samples from at least one time point; 12 of these had paired sequencing results from before and after chemo + H and 10 had successful sequencing from either time point. TP53 was the only significantly recurrently mutated gene in both pre- and post-treatment samples. MYC gene amplification was observed in four post-treatment tumors. Seven of 12 patients with paired samples showed acquired and/or clonally enriched alterations in cancer-related genes. One patient had an increased clonality putative activating mutation in ERBB2. Another patient acquired a clonal hotspot mutation in TP53. Other genomic changes acquired in post-treatment specimens included alterations in NOTCH2, STIL, PIK3CA, and GATA3. There was no significant change in median ERBB2 CN (20.3 v 22.6; Wilcoxon P = .79) between paired samples. CONCLUSION ERBB2-positive BCs in young women displayed substantial genomic evolution after treatment with chemo + H. Approximately half of patients with paired samples demonstrated acquired and/or clonally enriched genomic changes in cancer genes. ERBB2 CN changes were uncommon. We identified several genes warranting exploration as potential mechanisms of resistance to therapy in this population.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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