EGFR, the Lazarus target for precision oncology in glioblastoma
The Lazarus effect is a rare condition that happens when someone seemingly dead shows signs of life. The epidermal growth factor receptor (EGFR) represents a target in the fatal neoplasm glioblastoma (GBM) that through a series of negative clinical trials has prompted a vocal subset of the neuro-oncology community to declare this target dead. However, an argument can be made that the core tenets of precision oncology were overlooked in the initial clinical enthusiasm over EGFR as a therapeutic target in GBM. Namely, the wrong drugs were tested on the wrong patients at the wrong time. Furthermore, new insights into the biology of EGFR in GBM vis-à-vis other EGFR-driven neoplasms, such as non-small cell lung cancer, and development of novel GBM-specific EGFR therapeutics resurrects this target for future studies. Here, we will examine the distinct EGFR biology in GBM, how it exacerbates the challenge of treating a CNS neoplasm, how these unique challenges have influenced past and present EGFR-targeted therapeutic design and clinical trials, and what adjustments are needed to therapeutically exploit EGFR in this devastating disease.
Authors
- Erin Smithberger
- David A. Nathanson (ORCID: https://orcid.org/0000-0002-4919-9159)
- Kasey Skinner (ORCID: https://orcid.org/0000-0003-4316-5959)
- Zev A. Binder (ORCID: https://orcid.org/0000-0003-1158-231X)
- C. Ryan Miller (ORCID: https://orcid.org/0000-0002-0096-8762)
- Frank B. Furnari (ORCID: https://orcid.org/0000-0003-1909-4361)
- Timothy F. Cloughesy (ORCID: https://orcid.org/0000-0002-8656-7483)
- Julia Ziebro
- Eva Zhao
- Donald M. O’Rourke (ORCID: https://orcid.org/0000-0002-8479-7314)
- Benjamin Lin (ORCID: https://orcid.org/0000-0001-9361-5917)
Institutions
- University of North Carolina at Chapel Hill (US)
Publication Details
- Journal
- UNC Libraries
- Published
- 2025-05-07
- DOI
- https://doi.org/10.17615/17ns-3g24
- Primary Topic
- Glioma Diagnosis and Treatment
- Type
- article
- Field-Weighted Citation Impact
- 0.00