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Published in: Brain Tumor Pathology 4/2017

01-10-2017 | Case Report

Encouraging option of multi-staged gross total resection for a C11orf-RelA fusion-positive supratentorial anaplastic ependymoma

Authors: Taishi Nakamura, Kohei Fukuoka, Junji Ikeda, Masahiro Yoshitomi, Naoko Udaka, Reo Tanoshima, Kensuke Tateishi, Shoji Yamanaka, Koichi Ichimura, Tetsuya Yamamoto

Published in: Brain Tumor Pathology | Issue 4/2017

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Abstract

Ependymomas are primary neuroepithelial malignancies that mainly occur during childhood, and arise from ependymal cells along the ventricular systems of the CNS. Recently, it was elucidated that two-thirds of supratentorial (ST) ependymomas harbor oncogenic fusions of RELA, whose protein product is the principal effector of canonical NF-κB signaling. RELA fusion proteins activate signaling for tumor proliferation and malignant progression, resulting in poorer prognoses in these patients compared to those in patients with other ST ependymomas. In this study, we encountered a case of C11orfRelA fusion-positive ST anaplastic ependymoma that was diagnosed in first tumor resection surgery of multi-staged gross total resection with molecular evidence. In ependymomas, regardless of tumor location or pathological grade, subtotal resection is associated with higher rates of mortality compared with GTR. Molecular analysis based on the application of recent molecular knowledge for ST ependymomas performs a role in appropriate and individualized treatment strategies.
Literature
1.
go back to reference Louis DN, Ohgaki H, Wiestler OD et al (2016) WHO classification of tumours of the central nervous system. IARC Publications, Lyon Louis DN, Ohgaki H, Wiestler OD et al (2016) WHO classification of tumours of the central nervous system. IARC Publications, Lyon
2.
go back to reference Nazar GB, Hoffman HJ, Becker LE et al (1990) Infratentorial ependymomas in childhood: prognostic factors and treatment. J Neurosurg 72:408–417CrossRefPubMed Nazar GB, Hoffman HJ, Becker LE et al (1990) Infratentorial ependymomas in childhood: prognostic factors and treatment. J Neurosurg 72:408–417CrossRefPubMed
3.
4.
go back to reference Pietsch T, Wohlers I, Goschzik T et al (2014) Supratentorial ependymomas of childhood carry C11orf95–RELA fusions leading to pathological activation of the NF-kappaB signaling pathway. Acta Neuropathol 127:609–611CrossRefPubMed Pietsch T, Wohlers I, Goschzik T et al (2014) Supratentorial ependymomas of childhood carry C11orf95–RELA fusions leading to pathological activation of the NF-kappaB signaling pathway. Acta Neuropathol 127:609–611CrossRefPubMed
6.
go back to reference Pajtler KW, Witt H, Sill M et al (2015) Molecular classification of ependymal tumors across all CNS compartments, histopathological grades, and age groups. Cancer Cell 27:728–743CrossRefPubMedPubMedCentral Pajtler KW, Witt H, Sill M et al (2015) Molecular classification of ependymal tumors across all CNS compartments, histopathological grades, and age groups. Cancer Cell 27:728–743CrossRefPubMedPubMedCentral
8.
9.
go back to reference Cage TA, Clark AJ, Aranda D et al (2013) A systematic review of treatment outcomes in pediatric patients with intracranial ependymomas. J Neurosurg Pediatr 11:673–681CrossRefPubMed Cage TA, Clark AJ, Aranda D et al (2013) A systematic review of treatment outcomes in pediatric patients with intracranial ependymomas. J Neurosurg Pediatr 11:673–681CrossRefPubMed
10.
go back to reference Massimino M, Solero CL, Garre ML et al (2011) Second-look surgery for ependymoma: the Italian experience. J Neurosurg Pediatr 8:246–250CrossRefPubMed Massimino M, Solero CL, Garre ML et al (2011) Second-look surgery for ependymoma: the Italian experience. J Neurosurg Pediatr 8:246–250CrossRefPubMed
11.
go back to reference Cartmill M, Hewitt M, Walker D et al (2001) The use of chemotherapy to facilitate surgical resection in pleomorphic xanthoastrocytoma: experience in a single case. Child’s Nerv Syst 17:563–566CrossRef Cartmill M, Hewitt M, Walker D et al (2001) The use of chemotherapy to facilitate surgical resection in pleomorphic xanthoastrocytoma: experience in a single case. Child’s Nerv Syst 17:563–566CrossRef
12.
go back to reference Valera ET, Serafini LN, Machado HR, Tone LG (2003) Complete surgical resection in children with low-grade astrocytomas after neoadjuvant chemotherapy. Child’s Nerv Syst 19:86–90 Valera ET, Serafini LN, Machado HR, Tone LG (2003) Complete surgical resection in children with low-grade astrocytomas after neoadjuvant chemotherapy. Child’s Nerv Syst 19:86–90
13.
go back to reference Valera ET, Machado HR, Santos AC et al (2005) The use of neoadjuvant chemotherapy to achieve complete surgical resection in recurring supratentorial anaplastic ependymoma. Child’s Nerv Syst 21:230–233CrossRef Valera ET, Machado HR, Santos AC et al (2005) The use of neoadjuvant chemotherapy to achieve complete surgical resection in recurring supratentorial anaplastic ependymoma. Child’s Nerv Syst 21:230–233CrossRef
14.
go back to reference Huang J, Barbera L, Brouwers M et al (2003) Does delay in starting treatment affect the outcomes of radiotherapy? A systematic review. J Clin Oncol 21:555–563CrossRefPubMed Huang J, Barbera L, Brouwers M et al (2003) Does delay in starting treatment affect the outcomes of radiotherapy? A systematic review. J Clin Oncol 21:555–563CrossRefPubMed
15.
go back to reference van den Bent MJ, Afra D, de Witte O et al (2005) Long-term efficacy of early versus delayed radiotherapy for low-grade astrocytoma and oligodendroglioma in adults: the EORTC 22845 randomised trial. Lancet 366:985–990CrossRefPubMed van den Bent MJ, Afra D, de Witte O et al (2005) Long-term efficacy of early versus delayed radiotherapy for low-grade astrocytoma and oligodendroglioma in adults: the EORTC 22845 randomised trial. Lancet 366:985–990CrossRefPubMed
Metadata
Title
Encouraging option of multi-staged gross total resection for a C11orf-RelA fusion-positive supratentorial anaplastic ependymoma
Authors
Taishi Nakamura
Kohei Fukuoka
Junji Ikeda
Masahiro Yoshitomi
Naoko Udaka
Reo Tanoshima
Kensuke Tateishi
Shoji Yamanaka
Koichi Ichimura
Tetsuya Yamamoto
Publication date
01-10-2017
Publisher
Springer Singapore
Published in
Brain Tumor Pathology / Issue 4/2017
Print ISSN: 1433-7398
Electronic ISSN: 1861-387X
DOI
https://doi.org/10.1007/s10014-017-0297-5

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