| Literature DB >> 25600839 |
Alba A Brandes1, Marco Bartolotti2, Gianluca Marucci3, Claudio Ghimenton4, Raffaele Agati5, Antonio Fioravanti6, Maurizio Mascarin7, Lorenzo Volpin8, Franco Ammannati9, Barbara Masotto10, Marina Paola Gardiman11, Dario De Biase12, Giovanni Tallini12, Girolamo Crisi13, Stefania Bartolini2, Enrico Franceschi2.
Abstract
Medulloblastoma is the most common central nervous system tumor in children, while it is extremely rare in adults. Multimodal treatment involving surgery, radiotherapy and chemotherapy can improve the prognosis of this disease, and recent advances in molecular biology have allowed the identification of molecular subgroups (WNT, SHH, Groups 3 and 4), each of which have different cytogenetic, mutational and gene expression signatures, demographics, histology and prognosis. The present review focuses on the state of the art for adult medulloblastoma treatment and on novel molecular advances and their future implications in the treatment of this disease.Entities:
Keywords: Adults; Medulloblastoma; SHH; Treatment; WNT
Mesh:
Year: 2014 PMID: 25600839 DOI: 10.1016/j.critrevonc.2014.12.016
Source DB: PubMed Journal: Crit Rev Oncol Hematol ISSN: 1040-8428 Impact factor: 6.312