FGFR1 Antibody Validation and Characterization of FGFR1 Protein Expression in ER+ Breast Cancer

Paula I. Gonzalez-Ericsson, Alberto Servetto, Luigi Formisano, Violeta Sánchez, Ingrid A. Mayer, Carlos L. Arteaga, Melinda E. Sanders

Research output: Contribution to journalArticlepeer-review

Abstract

Clinical trials in patients with ER+ breast cancer with or without FGFR pathway somatic alterations have shown limited clinical benefit from treatment with FGFR tyrosine kinase inhibitors alone or in combination with endocrine therapy. This is likely because of an inadequate predictive biomarker to select appropriate patients. In this study, we evaluated 4 anti-FGFR1 antibodies in breast cancer cell lines and patient-derived xenografts with FGFR1 amplification. We correlated D8E4 expression in 209 tumors from postmenopausal patients with stage I-III operable ER+ breast cancer with FGFR1 amplification status as determined by fluorescence in situ hybridization. FGFR1 amplification was identified in 10% of tumors (21/209), 80% of which exhibited membranous FGFR1 expression; however, only 50% of amplified cases showed strong, complete membranous staining (3+) based on established criteria to score HER2 by immunohistochemistry. These findings suggest the combined evaluation of FGFR1 status by immunohistochemistry and fluorescence in situ hybridization may need to be incorporated into the selection of patients for trials with FGFR inhibitors.

Original languageEnglish (US)
Pages (from-to)600-608
Number of pages9
JournalApplied Immunohistochemistry
Volume30
Issue number9
DOIs
StatePublished - Oct 1 2022

ASJC Scopus subject areas

  • Pathology and Forensic Medicine
  • Histology
  • Medical Laboratory Technology

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