PLoS ONE (Jan 2016)

Anti-Epidermal Growth Factor Receptor Gene Therapy for Glioblastoma.

  • Martin J Hicks,
  • Maria J Chiuchiolo,
  • Douglas Ballon,
  • Jonathan P Dyke,
  • Eric Aronowitz,
  • Kosuke Funato,
  • Viviane Tabar,
  • David Havlicek,
  • Fan Fan,
  • Dolan Sondhi,
  • Stephen M Kaminsky,
  • Ronald G Crystal

DOI
https://doi.org/10.1371/journal.pone.0162978
Journal volume & issue
Vol. 11, no. 10
p. e0162978

Abstract

Read online

Glioblastoma multiforme (GBM) is the most common and aggressive primary intracranial brain tumor in adults with a mean survival of 14 to 15 months. Aberrant activation of the epidermal growth factor receptor (EGFR) plays a significant role in GBM progression, with amplification or overexpression of EGFR in 60% of GBM tumors. To target EGFR expressed by GBM, we have developed a strategy to deliver the coding sequence for cetuximab, an anti-EGFR antibody, directly to the CNS using an adeno-associated virus serotype rh.10 gene transfer vector. The data demonstrates that single, local delivery of an anti-EGFR antibody by an AAVrh.10 vector coding for cetuximab (AAVrh.10Cetmab) reduces GBM tumor growth and increases survival in xenograft mouse models of a human GBM EGFR-expressing cell line and patient-derived GBM. AAVrh10.CetMab-treated mice displayed a reduction in cachexia, a significant decrease in tumor volume and a prolonged survival following therapy. Adeno-associated-directed delivery of a gene encoding a therapeutic anti-EGFR monoclonal antibody may be an effective strategy to treat GBM.