Current promising treatment strategy for glioblastoma multiform: A review

Glioblastoma multiform (GBM) is a heterogeneous group of primary neoplasm resistant to conventional therapies. Due to their infiltrative nature it not fully isolated by aggressive surgery, radiation and chemotherapy showing poor prognosis in glioma patients. Unfortunately, diagnosed patients die wit...

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Bibliographic Details
Published inOncology Reviews Vol. 13; no. 2; p. 417
Main Authors Bahadur, Sanjib, Sahu, Arvind Kumar, Baghel, Pragya, Saha, Suman
Format Journal Article Book Review
LanguageEnglish
Published Switzerland PAGEPress Publications 25.07.2019
PAGEPress Scientific Publications, Pavia, Italy
PAGEPress Publications, Pavia, Italy
Frontiers Media S.A
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Summary:Glioblastoma multiform (GBM) is a heterogeneous group of primary neoplasm resistant to conventional therapies. Due to their infiltrative nature it not fully isolated by aggressive surgery, radiation and chemotherapy showing poor prognosis in glioma patients. Unfortunately, diagnosed patients die within 1.5-2 year treatment schedule. Currently temozolomide (TMZ) is the first choice for the prognosis of GBM patients. TMZ metabolites methyl triazen imidazol carboxamide form complex with alkyl guanine alkyl transferase (O6 MGMT- DNA repair protein) induced DNA damage following resistance properties of TMZ and inhibit the overall survival of the patients. Last few decades different TMZ conjugated strategy is developed to overcome the resistance and enhance the chemotherapy efficacy. The main aim of this review is to introduce the new promising pharmaceutical candidates that significantly influence the therapeutic response of the TMZ in context of targeted therapy of glioblastoma patients. It is hoped that this proposed strategy are highly effective to overcome the current resistance limitations of TMZ in GBM patients and enhance the survival rate of the patients.
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Contributions: the authors contributed equally.
Conflicts of interest: the authors declare no potential conflicts of interest.
ISSN:1970-5565
1970-5557
1970-5565
1970-5557
DOI:10.4081/oncol.2019.417