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Natural History and Characteristics of ERBB2-mutated Hormone Receptor-positive Metastatic Breast Cancer: A Multi-institutional Retrospective Case-control Study from AACR Project GENIE.
LeNoue-Newton, Michele L; Chen, Sheau-Chiann; Stricker, Thomas; Hyman, David M; Blauvelt, Natalie; Bedard, Philippe L; Meric-Bernstam, Funda; Punglia, Rinaa S; Schrag, Deborah; Lepisto, Eva M; Andre, Fabrice; Smyth, Lillian; Dogan, Semih; Yu, Celeste; Wathoo, Chetna; Levy, Mia; Eli, Lisa D; Xu, Feng; Mann, Grace; Lalani, Alshad S; Ye, Fei; Micheel, Christine M; Arnedos, Monica.
Affiliation
  • LeNoue-Newton ML; Vanderbilt-Ingram Cancer Center, Vanderbilt University Medical Center, Nashville, Tennessee.
  • Chen SC; Department of Biostatistics, Vanderbilt University Medical Center, Nashville, Tennessee.
  • Stricker T; Department of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, Tennessee.
  • Hyman DM; Memorial Sloan Kettering Cancer Center, New York, New York.
  • Blauvelt N; Memorial Sloan Kettering Cancer Center, New York, New York.
  • Bedard PL; Division of Medical Oncology and Hematology, Department of Medicine, University of Toronto, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.
  • Meric-Bernstam F; Department of Investigational Cancer Therapeutics, Division of Cancer Medicine, MD Anderson Cancer Center, Houston, Texas.
  • Punglia RS; Department of Radiation Oncology, DFCI, Harvard Medical School, Boston, Massachusetts.
  • Schrag D; Division of Population Sciences and the Department of Medical Oncology, Dana-Farber/Harvard Cancer Center, Boston, Massachusetts.
  • Lepisto EM; Division of Population Sciences and the Department of Medical Oncology, Dana-Farber/Harvard Cancer Center, Boston, Massachusetts.
  • Andre F; Department of Medical Oncology, Gustave Roussy Cancer Campus, Villejuif, France.
  • Smyth L; INSERM Unit, U981, Gustave Roussy Cancer Campus, Villejuif, France.
  • Dogan S; Memorial Sloan Kettering Cancer Center, New York, New York.
  • Yu C; Department of Medical Oncology, Gustave Roussy Cancer Campus, Villejuif, France.
  • Wathoo C; INSERM Unit, U981, Gustave Roussy Cancer Campus, Villejuif, France.
  • Levy M; Division of Medical Oncology and Hematology, Department of Medicine, University of Toronto, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.
  • Eli LD; Department of Investigational Cancer Therapeutics, Division of Cancer Medicine, MD Anderson Cancer Center, Houston, Texas.
  • Xu F; Departments of Biomedical Informatics and Medicine, Division of Hematology/Oncology, and Vanderbilt-Ingram Cancer Center, Vanderbilt University Medical Center, Nashville, Tennessee.
  • Mann G; PUMA Biotechnology, Los Angeles, California.
  • Lalani AS; PUMA Biotechnology, Los Angeles, California.
  • Ye F; PUMA Biotechnology, Los Angeles, California.
  • Micheel CM; PUMA Biotechnology, Los Angeles, California.
  • Arnedos M; Department of Biostatistics, Vanderbilt University Medical Center, Nashville, Tennessee.
Clin Cancer Res ; 28(10): 2118-2130, 2022 05 13.
Article in En | MEDLINE | ID: mdl-35190802
ABSTRACT

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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Breast Neoplasms / Carcinoma, Lobular Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Female / Humans Language: En Journal: Clin Cancer Res Journal subject: NEOPLASIAS Year: 2022 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Breast Neoplasms / Carcinoma, Lobular Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Female / Humans Language: En Journal: Clin Cancer Res Journal subject: NEOPLASIAS Year: 2022 Document type: Article
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