Rindopepimut: an evidence-based review of its therapeutic potential in the treatment of EGFRvIII-positive glioblastoma

被引:44
作者
Babu, Ranjith [1 ]
Adamson, D. Cory [1 ]
机构
[1] Duke Univ, Med Ctr, Div Neurosurg, Durham, NC USA
关键词
CDX-110; EGFRvIII; glioblastoma; immunotherapy; PEPvIII;
D O I
10.2147/CE.S29001
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
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.
引用
收藏
页码:93 / 103
页数:11
相关论文
共 99 条
[1]
Intercellular transfer of the oncogenic receptor EGFrvIII by microvesicles derived from tumour cells [J].
Al-Nedawi, Khalid ;
Meehan, Brian ;
Micallef, Johann ;
Lhotak, Vladimir ;
May, Linda ;
Guha, Abhijit ;
Rak, Janusz .
NATURE CELL BIOLOGY, 2008, 10 (05) :619-U24
[2]
Mechanisms of Local Immunoresistance in Glioma [J].
Albesiano, Emilia ;
Han, James E. ;
Lim, Michael .
NEUROSURGERY CLINICS OF NORTH AMERICA, 2010, 21 (01) :17-+
[3]
Immunohistochemical detection of EGFRvIII in high malignancy grade astrocytomas and evaluation of prognostic significance [J].
Aldape, KD ;
Ballman, K ;
Furth, A ;
Buckner, JC ;
Giannini, C ;
Burger, PC ;
Scheithauer, BW ;
Jenkins, RB ;
James, CD .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2004, 63 (07) :700-707
[4]
Archer GE, 1999, CLIN CANCER RES, V5, P2646
[5]
BATRA SK, 1995, CELL GROWTH DIFFER, V6, P1251
[6]
Immune surveillance of mouse brain perivascular spaces by blood-borne macrophages [J].
Bechmann, I ;
Priller, J ;
Kovac, A ;
Böntert, M ;
Wehner, T ;
Klett, FF ;
Bohsung, J ;
Stuschke, M ;
Dirnagl, U ;
Nitsch, R .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2001, 14 (10) :1651-1658
[7]
BIGNER SH, 1990, CANCER RES, V50, P8017
[8]
Constitutive EGFR signaling confers a motile phenotype to neural stem cells [J].
Boockvar, JA ;
Kapitonov, D ;
Kapoor, G ;
Schouten, J ;
Counelis, GJ ;
Bogler, O ;
Snyder, EY ;
McIntosh, TK ;
O'Rourke, DM .
MOLECULAR AND CELLULAR NEUROSCIENCE, 2003, 24 (04) :1116-1130
[9]
BROOKS WH, 1976, CANCER, V37, P1869, DOI 10.1002/1097-0142(197604)37:4<1869::AID-CNCR2820370435>3.0.CO
[10]
2-Q