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Molecular Classification of Medulloblastoma

Medulloblastoma (MB) is one of the most frequent malignant brain tumors in children. The current standard treatment regimen consists of surgical resection, craniospinal irradiation, and adjuvant chemotherapy. Although these treatments have the potential to increase the survival of 70–80% of patients...

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Autores principales: KIJIMA, Noriyuki, KANEMURA, Yonehiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japan Neurosurgical Society 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5221779/
https://www.ncbi.nlm.nih.gov/pubmed/27238212
http://dx.doi.org/10.2176/nmc.ra.2016-0016
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author KIJIMA, Noriyuki
KANEMURA, Yonehiro
author_facet KIJIMA, Noriyuki
KANEMURA, Yonehiro
author_sort KIJIMA, Noriyuki
collection PubMed
description Medulloblastoma (MB) is one of the most frequent malignant brain tumors in children. The current standard treatment regimen consists of surgical resection, craniospinal irradiation, and adjuvant chemotherapy. Although these treatments have the potential to increase the survival of 70–80% of patients with MB, they are also associated with serious treatment-induced morbidity. The current risk stratification of MB is based on clinical factors, including age at presentation, metastatic status, and the presence of residual tumor following resection. In addition, recent genomic studies indicate that MB consists of at least four distinct molecular subgroups: WNT, sonic hedgehog (SHH), Group 3, and Group 4. WNT and SHH MBs are characterized by aberrations in the WNT and SHH signaling pathways, respectively. WNT MB has the best prognosis compared to the other MBs, while SHH MB has an intermediate prognosis. The underlying signaling pathways associated with Group 3 and 4 MBs have not been identified. Group 3 MB is frequently associated with metastasis, resulting in a poor prognosis, while Group 4 is sometimes associated with metastasis and has an intermediate prognosis. Group 4 is the most frequent MB and represents 35% of all MBs. These findings suggest that MB is a heterogeneous disease, and that MB subgroups have distinct molecular, demographic, and clinical characteristics. The molecular classification of MBs is redefining the risk stratification of patients with MB, and has the potential to identify new therapeutic strategies for the treatment of MB.
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spelling pubmed-52217792017-01-17 Molecular Classification of Medulloblastoma KIJIMA, Noriyuki KANEMURA, Yonehiro Neurol Med Chir (Tokyo) Review Article Medulloblastoma (MB) is one of the most frequent malignant brain tumors in children. The current standard treatment regimen consists of surgical resection, craniospinal irradiation, and adjuvant chemotherapy. Although these treatments have the potential to increase the survival of 70–80% of patients with MB, they are also associated with serious treatment-induced morbidity. The current risk stratification of MB is based on clinical factors, including age at presentation, metastatic status, and the presence of residual tumor following resection. In addition, recent genomic studies indicate that MB consists of at least four distinct molecular subgroups: WNT, sonic hedgehog (SHH), Group 3, and Group 4. WNT and SHH MBs are characterized by aberrations in the WNT and SHH signaling pathways, respectively. WNT MB has the best prognosis compared to the other MBs, while SHH MB has an intermediate prognosis. The underlying signaling pathways associated with Group 3 and 4 MBs have not been identified. Group 3 MB is frequently associated with metastasis, resulting in a poor prognosis, while Group 4 is sometimes associated with metastasis and has an intermediate prognosis. Group 4 is the most frequent MB and represents 35% of all MBs. These findings suggest that MB is a heterogeneous disease, and that MB subgroups have distinct molecular, demographic, and clinical characteristics. The molecular classification of MBs is redefining the risk stratification of patients with MB, and has the potential to identify new therapeutic strategies for the treatment of MB. The Japan Neurosurgical Society 2016-11 2016-05-26 /pmc/articles/PMC5221779/ /pubmed/27238212 http://dx.doi.org/10.2176/nmc.ra.2016-0016 Text en © 2016 The Japan Neurosurgical Society This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Review Article
KIJIMA, Noriyuki
KANEMURA, Yonehiro
Molecular Classification of Medulloblastoma
title Molecular Classification of Medulloblastoma
title_full Molecular Classification of Medulloblastoma
title_fullStr Molecular Classification of Medulloblastoma
title_full_unstemmed Molecular Classification of Medulloblastoma
title_short Molecular Classification of Medulloblastoma
title_sort molecular classification of medulloblastoma
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5221779/
https://www.ncbi.nlm.nih.gov/pubmed/27238212
http://dx.doi.org/10.2176/nmc.ra.2016-0016
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