Epidermal growth factor receptor and variant III targeted immunotherapy

Kendra L Congdon1, Patrick C Gedeon1, Carter M Suryadevara1

  • 1The Preston Robert Tisch Brain Tumor Center (K.L.C., P.C.G., C.M.S., J.H.S.); Division of Neurosurgery, Department of Surgery, Duke University Medical Center Durham, North Carolina (K.L.C., P.C.G., C.M.S., J.H.S.); Department of Biomedical Engineering, Duke University Durham, North Carolina (P.C.G.); Department of Pathology, Duke University Medical Center Durham, North Carolina (J.H.S.); Department of Immunology, The University of Texas M.D. Anderson Cancer Center Houston, Texas (H.G.C., L.J.N.C.); Division of Pediatrics, The University of Texas M.D. Anderson Cancer Center Houston, Texas (H.G.C., L.J.N.C.); Department of Neurosurgery, The University of Texas M.D. Anderson Cancer Center Houston, Texas (A.B.H.).

Neuro-Oncology
|October 25, 2014
PubMed
Summary

Selecting safe and effective targets is crucial for cancer immunotherapy. This review examines immunotherapeutic strategies for high-grade glioma targeting epidermal growth factor receptor and its variant III, emphasizing safety and efficacy.

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