4.7 Article

Natural History and Characteristics of ERBB2-mutated Hormone Receptor-positive Metastatic Breast Cancer: A Multi-institutional Retrospective Case-control Study from AACR Project GENIE

Journal

CLINICAL CANCER RESEARCH
Volume 28, Issue 10, Pages 2118-2130

Publisher

AMER ASSOC CANCER RESEARCH
DOI: 10.1158/1078-0432.CCR-21-0885

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Funding

  1. PUMA Biotechnology
  2. AACR
  3. Robert J. Kleberg, Jr and Helen C. Kleberg Foundation
  4. Cancer Center Support Grant (CCSG) [5P30CA068485-21]
  5. CCSG [3P30CA068485-22S4]
  6. Foundation Gustave Roussy
  7. Foundation ARC
  8. French NCI PHRC
  9. PRISM
  10. NIH/NCI Memorial Sloan Kettering Cancer Center Support Grant [P30 CA008748]
  11. Princess Margaret Cancer Foundation (PMCF)
  12. Sheikh Khalifa Bin Zayed Al Nahyan Institute for Personalized Cancer Therapy
  13. Cancer Prevention and Research Institute of Texas (CPRIT) Precision Oncology Decision Support Core [RP150535]
  14. Dana Farber Harvard Cancer Center Core Grant [2P30CA006516]
  15. National Center for Advancing Translational Sciences [UL1TR000445]
  16. American Association for Cancer Research

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The purpose of this study was to investigate the prognosis and phenotypic characteristics of hormone receptor-positive advanced breast cancer tumors with an ERBB2 mutation in the absence of HER2 amplification. The results showed that the presence of an ERBB2 mutation did not affect overall survival or treatment response. However, some differences in coexisting mutations were observed between the ERBB2-mutated and control groups.
Purpose: We wanted to determine the prognosis and the phenotypic characteristics of hormone receptor-positive advanced breast cancer tumors harboring an ERBB2 mutation in the absence of a HER2 amplification. Experimental Design: We retrospectively collected information from the American Association of Cancer Research-Genomics Evidence Neoplasia Information Exchange registry database from patients with hormone receptor-positive, HER2-negative, ERBB2-mutated advanced breast cancer. Phenotypic and co-mutational features, as well as response to treatment and outcome were compared with matched control cases ERBB2 wild type. Results: A total of 45 ERBB2-mutant cases were identified for 90 matched controls. The presence of an ERBB2 mutation was not associated with worse outcome determined by overall survival (OS) from first metastatic relapse. No significant differences were observed in phenotypic characteristics apart from higher lobular infiltrating subtype in the ERBB2-mutated group. ERBB2 mutation did not seem to have an impact in response to treatment or time-to-progression (TTP) to endocrine therapy compared with ERBB2 wild type. In the co-mutational analyses, CDH1 mutation was more frequent in the ERBB2-mutated group (FDR < 1). Although not significant, fewer co-occurring ESR1 mutations and more KRAS mutations were identified in the ERBB2-mutated group. Conclusions: ERBB2-activating mutation was not associated with a worse OS from time of first metastatic relapse, or differences in TTP on treatment as compared with a series of matched controls. Although not significant, differences in coexisting mutations (CDH1, ESR1, and KRAS) were noted between the ERBB2-mutated and the control group.

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