Efficacy of epidermal growth factor receptor targeting in advanced chordoma: case report and literature review

Simon G Launay1, Bruno Chetaille, Fanny Medina

  • 1Department of Medical Oncology, Institut Paoli-Calmettes, 232 bd Ste-Marguerite, Marseille, 13009, France.

BMC Cancer
|October 6, 2011
PubMed
Abstract

Insights

Advanced chordoma, a rare bone cancer, may respond to EGFR inhibitors like erlotinib after imatinib resistance. This case highlights a potential new treatment avenue for this challenging diagnosis.

Area of Science:

  • Oncology
  • Skeletal Tumors
  • Molecular Targeted Therapy

Background:

  • Chordomas are rare, low-grade malignant bone tumors originating from notochordal remnants.
  • These tumors exhibit slow growth, frequent local recurrence, and potential metastasis.
  • Standard chemotherapy is largely ineffective, though imatinib shows some antitumor activity.

Observation:

  • A 76-year-old patient with advanced, EGFR-overexpressing chordoma experienced disease progression on imatinib therapy.
  • The patient subsequently received erlotinib, an epidermal growth factor receptor (EGFR) inhibitor.

Findings:

  • The patient demonstrated a positive response to erlotinib, with treatment continuing for 12 months.
  • This represents the fourth reported case of advanced chordoma treated with an EGFR inhibitor.

Implications:

  • EGFR inhibitors show potential as a therapeutic strategy for advanced chordoma, particularly in cases resistant to imatinib.
  • Further investigation into EGFR targeting in chordoma is warranted, given the limited treatment options.