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Central Nervous System Tumors

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Abstract

Overall incidence for primary central nervous system (CNS) tumors is about 19.34/100,000 person-years, men generally have higher rates of primary malignant form, and the incidence rate is lower in children. CNS tumors show several clinical presentations, like slowness in comprehension, loss of mental activity, focal cerebral signs, or symptoms related to increase of intracranial pressure. Between all the CNS cancers, glioblastoma multiforme (GBM) is characterized by high incidence and mortality. Conventional protocols in GBM treatment include surgical resection followed by radiotherapy and systemic chemotherapy with alkylating compounds. The overall survival of GBM is about 1 year on average, and the drug efficacy is fairly limited due to the existence of alternative genetic or epigenetic pathways able to confer a strong chemoresistance. The development of new molecular analysis techniques targeting specific cancer pathways allowed finding new specific genes or proteins (LOH at some key genetic loci, EGFR, PTEN, p53, or MGMT) useful to predict cancer aggressiveness and response to the standard radio- or chemotherapy treatment. Moreover, these studies lead to the development of new drugs, aiming at targeted therapy, able to switch off specific genetic pathways involved in cancerogenesis. This chapter reviews different molecular factors also useful as prognostic elements and focuses on the most important phase I–II studies involved in CNS cancer treatment.

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Correspondence to Paolo Aloisi M.D. .

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Aloisi, P., Martella, F., Cerone, D., Porzio, G. (2012). Central Nervous System Tumors. In: Bologna, M. (eds) Biotargets of Cancer in Current Clinical Practice. Current Clinical Pathology. Humana Press. https://doi.org/10.1007/978-1-61779-615-9_1

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