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Published in: Journal of Neuro-Oncology 2/2018

Open Access 01-06-2018 | Laboratory Investigation

Medulloblastoma with transitional features between Group 3 and Group 4 is associated with good prognosis

Authors: Maria Łastowska, Joanna Trubicka, Magdalena Niemira, Magdalena Paczkowska-Abdulsalam, Agnieszka Karkucińska-Więckowska, Magdalena Kaleta, Monika Drogosiewicz, Marta Perek-Polnik, Adam Krętowski, Bożena Cukrowska, Wiesława Grajkowska, Bożenna Dembowska-Bagińska, Ewa Matyja

Published in: Journal of Neuro-Oncology | Issue 2/2018

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Abstract

Medulloblastoma, the most common malignant pediatric brain tumor, is a heterogeneous disease, with the existence of at least four molecular types: Wingless (WNT), Sonic Hedgehog (SHH), Group 3 and Group 4 tumors. The latter two groups, which can be identified by an application of multi-gene expression or methylation profiling, show sometimes ambiguous categorization and are still classified for diagnostic reason as non-SHH/non-WNT medulloblastomas in updated WHO 2016 classification. In order to better characterize non-SHH/non-WNT tumors, we applied the method based on the Nanostring nCounter Technology, using the 26 genes codeset in 68 uniformly treated medulloblastoma patients. This allowed for identification of tumors, which shared common Group 3 and Group 4 gene signatures. We recognized three transcriptional groups within non-WNT/non-SHH tumors: Group 3, Group 4 and the Intermediate 3/4 Group. Group 3, in line with previously published results, showed poor prognosis with survival rate < 40%, frequent metastases, large cell/anaplastic pathology and presence of tumors with MYCC amplification. This is in contrast to patients from the Intermediate 3/4 Group who showed the best survival rate (100%). Overall and progression free survival were better for this group than for Group 3 (p = 0.001, for both) and Group 4 (p = 0.064 and p = 0.066, respectively). Our work supports the view that within the non-WNT/non-SHH tumors different risk groups exist and that the current two groups classifier may be not sufficient for proper clinical categorization of individual patients.
Literature
1.
2.
go back to reference Kool M, Korshunov A, Remke M, Jones DTW, Schlanstein M, Northcott PA et al (2012) Molecular subgroups of medulloblastoma: an international meta-analysis of transcriptome, genetic aberrations, and clinical data of WNT, SHH, Group 3, and Group 4 medulloblastomas. Acta Neuropathol 123:473–484CrossRefPubMedPubMedCentral Kool M, Korshunov A, Remke M, Jones DTW, Schlanstein M, Northcott PA et al (2012) Molecular subgroups of medulloblastoma: an international meta-analysis of transcriptome, genetic aberrations, and clinical data of WNT, SHH, Group 3, and Group 4 medulloblastomas. Acta Neuropathol 123:473–484CrossRefPubMedPubMedCentral
3.
go back to reference Cho YJ, Tsherniak A, Tamayo P, Santagata S, Ligon A, Greulich H, Berhoukim R, Amani V, Goumnerova L, Eberhart CG, Lau CC, Olson JM, Gilbertson RJ, Gajjar A, Delattre O, Kool M, Ligon K, Meyerson M, Mesirov JP, Pomeroy SL (2011) Integrativegenomic analysis of medulloblastoma identifies amolecular subgroup that drives poor clinical outcome. J Clin Oncol 29:1424–1430CrossRefPubMed Cho YJ, Tsherniak A, Tamayo P, Santagata S, Ligon A, Greulich H, Berhoukim R, Amani V, Goumnerova L, Eberhart CG, Lau CC, Olson JM, Gilbertson RJ, Gajjar A, Delattre O, Kool M, Ligon K, Meyerson M, Mesirov JP, Pomeroy SL (2011) Integrativegenomic analysis of medulloblastoma identifies amolecular subgroup that drives poor clinical outcome. J Clin Oncol 29:1424–1430CrossRefPubMed
4.
go back to reference Northcott PA, Korshunov A, Witt H et al (2011) Medulloblastoma comprises four distinct molecular variants. J Clin Oncol 29:1408–1414CrossRefPubMed Northcott PA, Korshunov A, Witt H et al (2011) Medulloblastoma comprises four distinct molecular variants. J Clin Oncol 29:1408–1414CrossRefPubMed
6.
go back to reference Louis DN, Ohgaki K, Wiestler OD, Cavenee WK (2016) WHO Classification of tumours of the central nervous system. 4th edn, International Agency for Research on Cancer, Lyon, pp 184–189 Louis DN, Ohgaki K, Wiestler OD, Cavenee WK (2016) WHO Classification of tumours of the central nervous system. 4th edn, International Agency for Research on Cancer, Lyon, pp 184–189
7.
go back to reference Northcott PA, Shih D, Remke M et al (2012) Rapid, reliable, and reproducible molecular sub-grouping of clinical medulloblastoma samples. Acta Neuropathol 123:615–626CrossRefPubMed Northcott PA, Shih D, Remke M et al (2012) Rapid, reliable, and reproducible molecular sub-grouping of clinical medulloblastoma samples. Acta Neuropathol 123:615–626CrossRefPubMed
9.
go back to reference Łastowska M, Trubicka J, Niemira M, Paczkowska-Abdulsalam M, Karkucińska-Więckowska A, Kaleta M et al (2017) ALK expression is a novel marker for the WNT-activated type of pediatric medulloblastoma and an indicator of good prognosis for patients. Am J Surg Pathol 41(6):781–787CrossRefPubMed Łastowska M, Trubicka J, Niemira M, Paczkowska-Abdulsalam M, Karkucińska-Więckowska A, Kaleta M et al (2017) ALK expression is a novel marker for the WNT-activated type of pediatric medulloblastoma and an indicator of good prognosis for patients. Am J Surg Pathol 41(6):781–787CrossRefPubMed
10.
go back to reference Chang CH, Housepian EM, Herbert C Jr (1969) An operative staging system and a megavoltage radiotherapeutic technic for cerebellar medulloblastomas. Radiology 93:1351–1359CrossRefPubMed Chang CH, Housepian EM, Herbert C Jr (1969) An operative staging system and a megavoltage radiotherapeutic technic for cerebellar medulloblastomas. Radiology 93:1351–1359CrossRefPubMed
11.
go back to reference Łastowska M, Jurkiewicz E, Trubicka J, Daszkiewicz P, Drogosiewicz M, Malczyk K et al (2015) Contrast enhancement pattern predicts poor survival for patients with non-WNT/SHH medulloblastoma tumours. J Neuro-Oncol 123(1):65–73CrossRef Łastowska M, Jurkiewicz E, Trubicka J, Daszkiewicz P, Drogosiewicz M, Malczyk K et al (2015) Contrast enhancement pattern predicts poor survival for patients with non-WNT/SHH medulloblastoma tumours. J Neuro-Oncol 123(1):65–73CrossRef
12.
go back to reference Hovestadt V, Remke M, Kool M, Pietsch T, Northcott PA, Fischer R et al (2013) Robust molecular subgrouping and copy number profiling of medulloblastoma from small amounts of archival tumour material using high density DNA methylation arrays. Acta Neuropathol 125:913–916CrossRefPubMedPubMedCentral Hovestadt V, Remke M, Kool M, Pietsch T, Northcott PA, Fischer R et al (2013) Robust molecular subgrouping and copy number profiling of medulloblastoma from small amounts of archival tumour material using high density DNA methylation arrays. Acta Neuropathol 125:913–916CrossRefPubMedPubMedCentral
13.
go back to reference Pietsch T, Schmidt R, Remke M, Korshunov A, Hovestadt V, Jones DTW et al (2014) Prognostic significance of clinical, histopathological, and molecular characteristics of medulloblastomas in the prospective HIT2000 multicenter clinical trial cohort. Acta Neuropathol 128:137–149CrossRefPubMedPubMedCentral Pietsch T, Schmidt R, Remke M, Korshunov A, Hovestadt V, Jones DTW et al (2014) Prognostic significance of clinical, histopathological, and molecular characteristics of medulloblastomas in the prospective HIT2000 multicenter clinical trial cohort. Acta Neuropathol 128:137–149CrossRefPubMedPubMedCentral
14.
go back to reference Schwalbe EC, Williamson D, Lindsey JC, Hamilton D, Ryan SL, Megahed H et al (2013) DNA methylation profiling of medulloblastoma allows robust subclassification and improved outcome prediction using formalin-fixed biopsies. Acta Neuropathol 125:359–371CrossRefPubMedPubMedCentral Schwalbe EC, Williamson D, Lindsey JC, Hamilton D, Ryan SL, Megahed H et al (2013) DNA methylation profiling of medulloblastoma allows robust subclassification and improved outcome prediction using formalin-fixed biopsies. Acta Neuropathol 125:359–371CrossRefPubMedPubMedCentral
15.
go back to reference Schwalbe EC, Lindsey JC, Nakjang S, Crosier S, Smith AJ, Hicks D et al (2017) Novel molecular subgroups for clinical classification and outcome prediction in childhood medulloblastoma: a cohort study. Lancet Oncol 18(7):958–971CrossRefPubMedPubMedCentral Schwalbe EC, Lindsey JC, Nakjang S, Crosier S, Smith AJ, Hicks D et al (2017) Novel molecular subgroups for clinical classification and outcome prediction in childhood medulloblastoma: a cohort study. Lancet Oncol 18(7):958–971CrossRefPubMedPubMedCentral
Metadata
Title
Medulloblastoma with transitional features between Group 3 and Group 4 is associated with good prognosis
Authors
Maria Łastowska
Joanna Trubicka
Magdalena Niemira
Magdalena Paczkowska-Abdulsalam
Agnieszka Karkucińska-Więckowska
Magdalena Kaleta
Monika Drogosiewicz
Marta Perek-Polnik
Adam Krętowski
Bożena Cukrowska
Wiesława Grajkowska
Bożenna Dembowska-Bagińska
Ewa Matyja
Publication date
01-06-2018
Publisher
Springer US
Published in
Journal of Neuro-Oncology / Issue 2/2018
Print ISSN: 0167-594X
Electronic ISSN: 1573-7373
DOI
https://doi.org/10.1007/s11060-018-2797-5

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