Glioblastoma multiforme (GBM) is the most common primary brain tumor in adults and is universally fatal. Despite surgical resection, radiotherapy, and systemic chemotherapy, the median overall survival is less than 15 months. As current therapies are not tumor-specific, treatment commonly results in toxicity. The epidermal growth factor receptor variant III (EGFRvIII) is a naturally occurring mutant of EGFR and is expressed on approximately 20% to 30% of GBMs. As it is not expressed on normal cells, it is an ideal therapeutic target. Rindopepimut is a peptide vaccine which elicits EGFRvIII-specific humoral and cellular immune responses. Phase I and II clinical trials have demonstrated significantly higher progression-free and overall survival times in vaccinated patients with EGFRvIII-expressing GBM tumors. Side effects are minimal and mainly consist of hypersensitivity reactions. Due to the efficacy and safety of rindopepimut, it is a promising therapy for patients with GBM. Currently, rindopepimut is undergoing clinical testing in an international Phase III trial for newly diagnosed GBM and a Phase II trial for relapsed GBM.
Keyphrases
- epidermal growth factor receptor
- phase iii
- clinical trial
- immune response
- open label
- tyrosine kinase
- newly diagnosed
- phase ii
- induced apoptosis
- advanced non small cell lung cancer
- early stage
- small cell lung cancer
- radiation therapy
- squamous cell carcinoma
- acute myeloid leukemia
- double blind
- placebo controlled
- locally advanced
- acute lymphoblastic leukemia
- oxidative stress
- randomized controlled trial
- dendritic cells
- free survival
- multiple myeloma
- hodgkin lymphoma
- signaling pathway
- diffuse large b cell lymphoma
- rectal cancer
- cell proliferation
- endoplasmic reticulum stress
- smoking cessation
- drug induced