Toxin-Based Targeted Therapy for Malignant Brain Tumors

被引:19
作者
Chandramohan, Vidyalakshmi [1 ]
Sampson, John H. [2 ]
Pastan, Ira [3 ]
Bigner, Darell D. [1 ]
机构
[1] Duke Univ, Med Ctr, Dept Pathol, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Dept Surg, Durham, NC 27710 USA
[3] NCI, Mol Biol Lab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA
来源
CLINICAL & DEVELOPMENTAL IMMUNOLOGY | 2012年
关键词
GROWTH-FACTOR RECEPTOR; CONVECTION-ENHANCED DELIVERY; IL4-PSEUDOMONAS EXOTOXIN NBI-3001; PLASMINOGEN-ACTIVATOR RECEPTOR; INTERLEUKIN-4; IL-4; RECEPTORS; SINGLE-CHAIN ANTIBODY; FACTOR FUSION PROTEIN; CELL-CARCINOMA-CELLS; DIPHTHERIA-TOXIN; PSEUDOMONAS EXOTOXIN;
D O I
10.1155/2012/480429
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Despite advances in conventional treatment modalities for malignant brain tumors-surgery, radiotherapy, and chemotherapy-the prognosis for patients with high-grade astrocytic tumor remains dismal. The highly heterogeneous and diffuse nature of astrocytic tumors calls for the development of novel therapies. Advances in genomic and proteomic research indicate that treatment of brain tumor patients can be increasingly personalized according to the characteristics of the targeted tumor and its environment. Consequently, during the last two decades, a novel class of investigative drug candidates for the treatment of central nervous system neoplasia has emerged: recombinant fusion protein conjugates armed with cytotoxic agents targeting tumor-specific antigens. The clinical applicability of the tumor-antigen-directed cytotoxic proteins as a safe and viable therapy for brain tumors is being investigated. Thus far, results from ongoing clinical trials are encouraging, as disease stabilization and patient survival prolongation have been observed in at least 109 cases. This paper summarizes the major findings pertaining to treatment with the different antiglioma cytotoxins at the preclinical and clinical stages.
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页数:15
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