Prospect of rindopepimut in the treatment of glioblastoma

被引:37
作者
Elsamadicy, Aladine A. [1 ,2 ]
Chongsathidkiet, Pakawat [1 ,2 ,3 ]
Desai, Rupen [4 ]
Woroniecka, Karolina [1 ,2 ,3 ]
Farber, S. Harrison [1 ,2 ]
Fecci, Peter E. [1 ,2 ,3 ]
Sampson, John H. [1 ,2 ,3 ]
机构
[1] Duke Univ, Med Ctr, Dept Neurosurg, Duke Brain Tumor Immunotherapy Program, Box 3050, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Preston Robert Tisch Brain Tumor Ctr, Durham, NC USA
[3] Duke Univ, Med Ctr, Dept Pathol, Durham, NC 27710 USA
[4] Washington Univ, Sch Med St Louis, Dept Neurosurg, St Louis, MO USA
关键词
Glioblastoma; immunotherapy; clinical trials; rindopepimut; peptide vaccine; EGFRvIII; EPIDERMAL-GROWTH-FACTOR; KEYHOLE LIMPET HEMOCYANIN; CELL-CYCLE CHECKPOINTS; FACTOR RECEPTOR GENE; PEPTIDE VACCINATION; PRIMARY BRAIN; PHASE-II; EGFRVIII; MULTIFORME; EXPRESSION;
D O I
10.1080/14712598.2017.1299705
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Introduction: Rindopepimut (CDX-110) is a peptide vaccine that targets epidermal growth factor receptor variant III (EGFRvIII), a tumor-specific epitope expressed in the most common and lethal primary malignant neoplasm of the brain - glioblastoma (GBM).Areas covered: The EGFRvIII mutation introduces an 801 base pair in-frame deletion of the extracellular domain of the transmembrane tyrosine kinase, resulting in constitutive kinase activity, amplification of cell growth, and inhibition of apoptosis. Rindopepimut contains a 14mer amino acid peptide spanning the EGFRvIII mutation site that is conjugated to keyhole limpet hemocyanin (KLH). The EGFRvIII neoantigen is exclusively present on GBM cells, providing rindopepimut tumor-specific activity. The authors review rindopepimut's clinical efficacy, administration, safety, and prospects in the treatment of GBM.Expert opinion: Rindopepimut showed clinical benefit and significant efficacy in phase II clinical trials, including as part of a multi-immunotherapy approach. A phase III clinical trial was terminated early, however, as it was deemed likely the study would fail to meet its primary endpoint. Longer term and sub-group analyses will be necessary to better understand rindopepimut's future role in GBM therapy.
引用
收藏
页码:507 / 513
页数:7
相关论文
共 51 条
[1]   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
[2]   Rindopepimut: an evidence-based review of its therapeutic potential in the treatment of EGFRvIII-positive glioblastoma [J].
Babu, Ranjith ;
Adamson, D. Cory .
CORE EVIDENCE, 2012, 7 :93-103
[3]  
BIGNER SH, 1990, CANCER RES, V50, P8017
[4]   Brain tumor epidemiology: Consensus from the Brain Tumor Epidemiology Consortium [J].
Bondy, Melissa L. ;
Scheurer, Michael E. ;
Malmer, Beatrice ;
Barnholtz-Sloan, Jill S. ;
Davis, Faith G. ;
Il'Yasova, Dora ;
Kruchko, Carol ;
McCarthy, Bridget J. ;
Rajaraman, Preetha ;
Schwartzbaum, Judith A. ;
Sadetzki, Siegal ;
Schlehofer, Brigitte ;
Tihan, Tarik ;
Wiemels, Joseph L. ;
Wrensch, Margaret ;
Buffler, Patricia A. .
CANCER, 2008, 113 (07) :1953-1968
[5]   Early-Stage Progress on Glioma Vaccines [J].
Brower, Vicki .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2011, 103 (18) :1361-1362
[6]  
COHEN S, 1962, J BIOL CHEM, V237, P1555
[7]   IDH mutations in glioma and acute myeloid leukemia [J].
Dang, Lenny ;
Jin, Shengfang ;
Su, Shinsan M. .
TRENDS IN MOLECULAR MEDICINE, 2010, 16 (09) :387-397
[8]   Medical progress: Brain tumors [J].
DeAngelis, LM .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (02) :114-123
[9]   Emerging immunotherapies for glioblastoma [J].
Desai, Rupen ;
Suryadevara, Carter M. ;
Batich, Kristen A. ;
Farber, S. Harrison ;
Sanchez-Perez, Luis ;
Sampson, John H. .
EXPERT OPINION ON EMERGING DRUGS, 2016, 21 (02) :133-145
[10]  
EKSTRAND AJ, 1991, CANCER RES, V51, P2164