EGFR, the Lazarus target for precision oncology in glioblastoma

Author:

Lin Benjamin1,Ziebro Julia1,Smithberger Erin12,Skinner Kasey R13ORCID,Zhao Eva4,Cloughesy Timothy F5,Binder Zev A6,O’Rourke Donald M6,Nathanson David A4,Furnari Frank B78,Miller C Ryan1ORCID

Affiliation:

1. Department of Pathology, Division of Neuropathology, Heersink School of Medicine, University of Alabama at Birmingham , Birmingham, Alabama , USA

2. Pathobiology and Translational Sciences Program, School of Medicine, University of North Carolina , Chapel Hill, North Carolina , USA

3. Neurosciences Curriculum, School of Medicine, University of North Carolina , Chapel Hill, North Carolina , USA

4. Department of Molecular and Medical Pharmacology, David Geffen School of Medicine, University of California, Los Angeles , Los Angeles, California , USA

5. Department of Neurology, David Geffen School of Medicine, University of California, Los Angeles , Los Angeles, California , USA

6. Department of Neurosurgery and Glioblastoma Translational Center of Excellence, Abramson Cancer Center, Perelman School of Medicine, University of Pennsylvania , Philadelphia, Pennsylvania , USA

7. Department of Medicine, Division of Regenerative Medicine, University of California, San Diego , San Diego, California , USA

8. Ludwig Cancer Research , San Diego, California , USA

Abstract

AbstractThe 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.

Funder

Medical Scientist Training Program

UAB Heersink School of Medicine

National Cancer Institute

National Institute of Neurological Disorders and Stroke

Templeton Family Initiative in Neuro-Oncology, The Maria and Gabriele Troiano Brain Cancer Immunotherapy

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Neurology (clinical),Oncology

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