ERBB2 emerges as a new target for colorectal cancer

Eirini Pectasides1, Adam J Bass2

  • 1Division of Hematology and Oncology, Beth Israel Deaconess Hospital, Boston, Massachusetts. Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.

Cancer Discovery
|August 6, 2015
PubMed

Insights

ERBB2 alterations are found in 7% of colorectal cancers. These changes can predict resistance to anti-EGFR drugs and identify patients for ERBB2-targeted treatments.

Area of Science:

  • Oncology
  • Molecular Biology
  • Genetics

Background:

  • Colorectal cancer (CRC) is a significant global health concern.
  • Epidermal growth factor receptor (EGFR) targeted therapies are standard treatments for some metastatic CRCs.
  • Mechanisms of resistance to anti-EGFR therapy are critical to understand for improving patient outcomes.

Purpose of the Study:

  • To investigate the role of ERBB2 (also known as HER2) mutations and amplifications in colorectal cancer.
  • To determine if ERBB2 alterations are associated with resistance to anti-EGFR therapy.
  • To explore the potential of ERBB2 as a predictive biomarker for ERBB2-directed therapies in CRC.

Main Methods:

  • Analysis of ERBB2 gene status (mutations and amplifications) in a cohort of colorectal cancer patients.
  • Correlation of ERBB2 alterations with clinical response to anti-EGFR therapy.
  • Evaluation of ERBB2 alterations as potential targets for novel therapeutic strategies.

Main Results:

  • ERBB2 mutations and amplifications were identified in approximately 7% of the studied colorectal cancer cases.
  • The presence of ERBB2 alterations may indicate a poorer response to standard anti-EGFR therapies.
  • ERBB2 alterations represent a potential actionable target for specific patient subgroups.

Conclusions:

  • ERBB2 alterations are an emerging factor in colorectal cancer biology.
  • Identifying ERBB2 alterations can help stratify patients for anti-EGFR therapy.
  • ERBB2-directed therapies may offer a new treatment avenue for a subset of colorectal cancer patients with these specific genetic changes.

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