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Published in: Journal of Neuro-Oncology 3/2018

01-02-2018 | Clinical Study

Characteristics of cerebellar glioblastomas in adults

Authors: Thiébaud Picart, Marc Barritault, Julien Berthillier, David Meyronet, Alexandre Vasiljevic, Didier Frappaz, Jérôme Honnorat, Emmanuel Jouanneau, Delphine Poncet, François Ducray, Jacques Guyotat

Published in: Journal of Neuro-Oncology | Issue 3/2018

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Abstract

Adult cerebellar glioblastomas (cGBM) are rare and their characteristics remain to be fully described. We analyzed the characteristics of 17 adult patients with cGBM and compared them to a series of 103 patients presenting a supra-tentorial glioblastoma (stGBM). The mean age at GBMc diagnosis was 53.4 years (range 28–77). A history of neurofibromatosis type I was noted in 3 patients. cGBM were hemispheric in 10 patients (58.8%), only vermian in 4 patients (23.5%), and both vermian and hemispheric in 3 patients (17.7%). A H3 K27M mutation was identified in 3/14 patients, a TERT promoter mutation in 3/14 patients and a methylated MGMT promoter in 3/14 patients. None of the patients (0/14) harbored an EGFR amplification, an IDH or a BRAF mutation. Association with neurofibromatosis type I and H3K27M mutations were mutually exclusive. Compared with stGBM, cGBM occurred in younger patients (53.4 vs. 63.2, p = 0.02), were more frequently associated with neurofibromatosis type I (18 vs. 1%, p = 0.009) and with a H3 K27M mutation (21 vs. 3%, p = 0.02). They also tended to have a more frequent multifocal presentation at diagnosis (21 vs. 4.3%, p = 0.06), more frequently resulted in leptomeningeal or intra-axial metastasis (44.5 vs. 5%, p = 0.002) and were associated with a shorter median overall survival (5.9 vs. 14.2 months, p = 0.004). The present study suggests that adult cGBM differ from their supra-tentorial counterpart and constitute a heterogeneous group of IDH wild-type gliomas with at least two subgroups, one associated with H3K27M mutations and the other with neurofibromatosis type I.
Literature
1.
go back to reference Chamberlain MC, Silver P, Levin VA (1990) Poorly differentiated gliomas of the cerebellum. A study of 18 patients. Cancer 65:337–340CrossRefPubMed Chamberlain MC, Silver P, Levin VA (1990) Poorly differentiated gliomas of the cerebellum. A study of 18 patients. Cancer 65:337–340CrossRefPubMed
2.
go back to reference Bi WL, Chiocca EA (2013) Adult cerebellar glioblastomas: a distinct entity or parcel of the whole? World Neurosurg 80(6):181–183CrossRef Bi WL, Chiocca EA (2013) Adult cerebellar glioblastomas: a distinct entity or parcel of the whole? World Neurosurg 80(6):181–183CrossRef
3.
go back to reference Mattos JP, Marenco HA, Campos JM et al (2006) Cerebellar glioblastoma multiforme in an dult. Arq Neuropsiquiatr 64(1):132–135CrossRefPubMed Mattos JP, Marenco HA, Campos JM et al (2006) Cerebellar glioblastoma multiforme in an dult. Arq Neuropsiquiatr 64(1):132–135CrossRefPubMed
4.
go back to reference Levine SA, McKeever PE, Greenberg HS (1987) Primary cerebellar glioblastoma multiforme. J Neuro-Oncology 5:231–236CrossRef Levine SA, McKeever PE, Greenberg HS (1987) Primary cerebellar glioblastoma multiforme. J Neuro-Oncology 5:231–236CrossRef
5.
go back to reference Adams H, Chaichana KL, Avendaño J et al (2013) Adult cerebellar glioblastoma: understanding survival and prognostic factors using a population-based database from 1973 to 2009. World Neurosurg 80(6):237–243CrossRef Adams H, Chaichana KL, Avendaño J et al (2013) Adult cerebellar glioblastoma: understanding survival and prognostic factors using a population-based database from 1973 to 2009. World Neurosurg 80(6):237–243CrossRef
6.
go back to reference Akimoto J, Fukami S, Tsutsumi M et al (2009) Radiopathological characteristics of cerebellar malignant glioma in adults. Brain Tumor Pathol 26:59CrossRefPubMed Akimoto J, Fukami S, Tsutsumi M et al (2009) Radiopathological characteristics of cerebellar malignant glioma in adults. Brain Tumor Pathol 26:59CrossRefPubMed
7.
go back to reference Babu R, Sharma R, Karikari IO et al (2013) Outcome and prognostic factors in adult cerebellar glioblastoma. J Clin Neurosci 20(8):1117–1121CrossRefPubMed Babu R, Sharma R, Karikari IO et al (2013) Outcome and prognostic factors in adult cerebellar glioblastoma. J Clin Neurosci 20(8):1117–1121CrossRefPubMed
8.
go back to reference Gopalakrishnan CV, Dhakoji A, Nair S et al (2012) A retrospective study of primary cerebellar glioblastoma multiforme in adults. J Clin Neurosci 19(12):1684–1688CrossRefPubMed Gopalakrishnan CV, Dhakoji A, Nair S et al (2012) A retrospective study of primary cerebellar glioblastoma multiforme in adults. J Clin Neurosci 19(12):1684–1688CrossRefPubMed
9.
go back to reference Grahovac G, Tomac D, Lambasa S et al (2009) Cerebellar glioblastomas: pathophysiology, clinical presentation and management. Acta Neurochir 151(6):653–657CrossRefPubMed Grahovac G, Tomac D, Lambasa S et al (2009) Cerebellar glioblastomas: pathophysiology, clinical presentation and management. Acta Neurochir 151(6):653–657CrossRefPubMed
10.
go back to reference Gupta V, Goyal A, Sinha S et al (2003) Glioblastoma of the cerebellum. A report of 3 cases. J Neurosurg Sci 47(3):157–164PubMed Gupta V, Goyal A, Sinha S et al (2003) Glioblastoma of the cerebellum. A report of 3 cases. J Neurosurg Sci 47(3):157–164PubMed
11.
go back to reference Hur H, Jung S, Jung TY et al (2008) Cerebellar glioblastoma multiforme in an adult? J Korean Neurosurg 43:194–197CrossRef Hur H, Jung S, Jung TY et al (2008) Cerebellar glioblastoma multiforme in an adult? J Korean Neurosurg 43:194–197CrossRef
13.
go back to reference Lakičević G, Arnautović K, Mužević D et al (2014) Cerebellar glioblastoma multiforme presenting as hypertensive cerebellar hemorrhage: case report. J Neurol Surg Rep 75(1):e117–e121CrossRefPubMedPubMedCentral Lakičević G, Arnautović K, Mužević D et al (2014) Cerebellar glioblastoma multiforme presenting as hypertensive cerebellar hemorrhage: case report. J Neurol Surg Rep 75(1):e117–e121CrossRefPubMedPubMedCentral
14.
go back to reference Linsenmann T, Monoranu CM, Vince GH et al (2014) Long-term tumor control of spinal dissemination of cerebellar glioblastoma multiforme by combined adjuvant bevacizumab antibody therapy: a case report. BMC Res Notes 7:496CrossRefPubMedPubMedCentral Linsenmann T, Monoranu CM, Vince GH et al (2014) Long-term tumor control of spinal dissemination of cerebellar glioblastoma multiforme by combined adjuvant bevacizumab antibody therapy: a case report. BMC Res Notes 7:496CrossRefPubMedPubMedCentral
15.
go back to reference Miller EM, Mani RL, Townsend JJ (1976) Cerebellar glioblastoma multiforme in an adult. Surg Neurol 5(6):341–343PubMed Miller EM, Mani RL, Townsend JJ (1976) Cerebellar glioblastoma multiforme in an adult. Surg Neurol 5(6):341–343PubMed
17.
go back to reference Saito T, Hama S, Kajiwara Y et al (2006) Prognosis of cerebellar glioblastomas: correlation between prognosis and immunoreactivity for epidermal growth factor receptor compared with supratentorial glioblastomas. Anticancer Res 26:1351–1358PubMed Saito T, Hama S, Kajiwara Y et al (2006) Prognosis of cerebellar glioblastomas: correlation between prognosis and immunoreactivity for epidermal growth factor receptor compared with supratentorial glioblastomas. Anticancer Res 26:1351–1358PubMed
19.
go back to reference Stark AAM, Maslehaty H, Hugo HH et al (2010) Glioblastoma of the cerebellum and brainstem. J Clin Neurosci 17:1248–1251CrossRefPubMed Stark AAM, Maslehaty H, Hugo HH et al (2010) Glioblastoma of the cerebellum and brainstem. J Clin Neurosci 17:1248–1251CrossRefPubMed
20.
go back to reference Tamaki T, Eguchi T, Sakamoto M et al (2004) Glioblastoma multiforme of the cerebellum in an elderly man. J Chin Med Assoc 67(6):301–304PubMed Tamaki T, Eguchi T, Sakamoto M et al (2004) Glioblastoma multiforme of the cerebellum in an elderly man. J Chin Med Assoc 67(6):301–304PubMed
21.
go back to reference Tsung AJ, Prabhu SS, Lei X et al (2011) Cerebellar glioblastoma: a retrospective review of 21 patients at a single institution. J Neurooncol 105:555–562CrossRefPubMed Tsung AJ, Prabhu SS, Lei X et al (2011) Cerebellar glioblastoma: a retrospective review of 21 patients at a single institution. J Neurooncol 105:555–562CrossRefPubMed
22.
go back to reference Weber DC, Miller RC, Villà S et al (2006) Outcome and prognosis factors in cerebellar glioblastoma multiforme in adults: a retrospective study from the rare cancer network. Int J Radiat Oncol Biol Phys 1 66(1):179–186CrossRefPubMed Weber DC, Miller RC, Villà S et al (2006) Outcome and prognosis factors in cerebellar glioblastoma multiforme in adults: a retrospective study from the rare cancer network. Int J Radiat Oncol Biol Phys 1 66(1):179–186CrossRefPubMed
24.
go back to reference Wen PY, Macdonald DR, Reardon DA et al (2010) Updated response assessment criteria for high-grade gliomas: response assessment in neuro-oncology working group. J Clin Oncol 28:1963–1972CrossRefPubMed Wen PY, Macdonald DR, Reardon DA et al (2010) Updated response assessment criteria for high-grade gliomas: response assessment in neuro-oncology working group. J Clin Oncol 28:1963–1972CrossRefPubMed
25.
go back to reference Meyronet D, Esteban-Mader M, Bonnet C et al (2017) Characteristics of H3 K27M-mutant gliomas in adults. Neuro-Oncology. 19:1127CrossRefPubMed Meyronet D, Esteban-Mader M, Bonnet C et al (2017) Characteristics of H3 K27M-mutant gliomas in adults. Neuro-Oncology. 19:1127CrossRefPubMed
26.
go back to reference Walter T, van Brakel B, Vercherat C et al (2015) O6-methylguanine-DNA methyltransferase status in neuroendocrine tumours: prognostic relevance and association with response to alkylating agents. Br J Cancer 112(3):523–531CrossRefPubMedPubMedCentral Walter T, van Brakel B, Vercherat C et al (2015) O6-methylguanine-DNA methyltransferase status in neuroendocrine tumours: prognostic relevance and association with response to alkylating agents. Br J Cancer 112(3):523–531CrossRefPubMedPubMedCentral
27.
go back to reference Idbaih A, Criniere E, Marie Y et al (2008) Gene amplification is a poor prognostic factor in anaplastic oligodendrogliomas. Neuro-Oncology 10(4):540–547CrossRefPubMedPubMedCentral Idbaih A, Criniere E, Marie Y et al (2008) Gene amplification is a poor prognostic factor in anaplastic oligodendrogliomas. Neuro-Oncology 10(4):540–547CrossRefPubMedPubMedCentral
28.
go back to reference Takahashi Y, Makino K, Nakamura H et al (2014) Clinical characteristics and pathogenesis of cerebellar glioblastoma. Mol Med Rep 10(5):2383–2388CrossRefPubMed Takahashi Y, Makino K, Nakamura H et al (2014) Clinical characteristics and pathogenesis of cerebellar glioblastoma. Mol Med Rep 10(5):2383–2388CrossRefPubMed
29.
go back to reference Kuroiwa T, Numaguchi Y, Rothman MI et al (1995) Posterior fossa glioblastoma multiforme: MR findings. Am J Neuroradiol 16:583–589PubMed Kuroiwa T, Numaguchi Y, Rothman MI et al (1995) Posterior fossa glioblastoma multiforme: MR findings. Am J Neuroradiol 16:583–589PubMed
30.
go back to reference Utsuki S, Oka H, Miyajima Y et al (2012) Adult cerebellar glioblastoma cases have different characteristics from supratentorial glioblastoma. Brain Tumor Pathol 29(2):87–95CrossRefPubMed Utsuki S, Oka H, Miyajima Y et al (2012) Adult cerebellar glioblastoma cases have different characteristics from supratentorial glioblastoma. Brain Tumor Pathol 29(2):87–95CrossRefPubMed
31.
go back to reference Kulkarni AV, Becker LE, Jay V et al (1999) Primary cerebellar glioblastomas multiforme in children. Report of four cases. J Neurosurg 90(3):546–550CrossRefPubMed Kulkarni AV, Becker LE, Jay V et al (1999) Primary cerebellar glioblastomas multiforme in children. Report of four cases. J Neurosurg 90(3):546–550CrossRefPubMed
32.
go back to reference Zito JL, Siva A, Smith TW et al (1983) Glioblastoma of the cerebellum. Computed tomographic and pathologic considerations. Surg Neurol 19(4):373–378CrossRefPubMed Zito JL, Siva A, Smith TW et al (1983) Glioblastoma of the cerebellum. Computed tomographic and pathologic considerations. Surg Neurol 19(4):373–378CrossRefPubMed
33.
go back to reference Pato-Pato A, Cimas-Hernando I, Lorenzo-González JR et al (2004) Cerebellar glioblastoma multiforme: a case report. Rev Neurol 38(9):839–842PubMed Pato-Pato A, Cimas-Hernando I, Lorenzo-González JR et al (2004) Cerebellar glioblastoma multiforme: a case report. Rev Neurol 38(9):839–842PubMed
34.
go back to reference Lobão CAF, Barbosa AS, Nogueira J et al (2008) Cerebellar glioblastoma mutiforme in an adult. Arq Neuropsiquiatr 66(4):879–880CrossRefPubMed Lobão CAF, Barbosa AS, Nogueira J et al (2008) Cerebellar glioblastoma mutiforme in an adult. Arq Neuropsiquiatr 66(4):879–880CrossRefPubMed
35.
go back to reference Singla N, Kapoor A, Savardekar A et al (2016) Malignant cerebellar peduncle lesions - rapid progression and poor outcome. Surg Neurol Int 7:S170–S173CrossRefPubMedPubMedCentral Singla N, Kapoor A, Savardekar A et al (2016) Malignant cerebellar peduncle lesions - rapid progression and poor outcome. Surg Neurol Int 7:S170–S173CrossRefPubMedPubMedCentral
36.
go back to reference Sturm D, Witt H, Hovestadt V et al (2012) Hotspot mutations in H3F3A and IDH1 define distinct epigenetic and biological subgroups of glioblastoma. Cancer Cell 22(4):425–437CrossRefPubMed Sturm D, Witt H, Hovestadt V et al (2012) Hotspot mutations in H3F3A and IDH1 define distinct epigenetic and biological subgroups of glioblastoma. Cancer Cell 22(4):425–437CrossRefPubMed
37.
go back to reference Kawarabuki K, Ohta T, Hashimoto N et al (2005) Cerebellar glioblastoma genetically defined as a secondary one. Clin Neuropathol 24(2):64–68PubMed Kawarabuki K, Ohta T, Hashimoto N et al (2005) Cerebellar glioblastoma genetically defined as a secondary one. Clin Neuropathol 24(2):64–68PubMed
38.
go back to reference Yang SY, Wang KC, Cho BK et al (2005) Radiation-induced cerebellar glioblastoma at the site of a treated medulloblastoma: case report. J Neurosurg 102(4 Suppl):417–422PubMed Yang SY, Wang KC, Cho BK et al (2005) Radiation-induced cerebellar glioblastoma at the site of a treated medulloblastoma: case report. J Neurosurg 102(4 Suppl):417–422PubMed
39.
go back to reference Ceccarelli M, Barthel FP, Malta TM et al (2016) Molecular profiling reveals biologically discrete subsets and pathways of progression in diffuse glioma. Cell 164(3):550–563CrossRefPubMedPubMedCentral Ceccarelli M, Barthel FP, Malta TM et al (2016) Molecular profiling reveals biologically discrete subsets and pathways of progression in diffuse glioma. Cell 164(3):550–563CrossRefPubMedPubMedCentral
41.
go back to reference Gerrit H, Gielen M, Gessi J, Hammes et al (2013) H3F3A K27M mutation in pediatric CNS tumors: a marker for diffuse high-grade astrocytoma. Am J Clin Pathol 139(3):345–349CrossRef Gerrit H, Gielen M, Gessi J, Hammes et al (2013) H3F3A K27M mutation in pediatric CNS tumors: a marker for diffuse high-grade astrocytoma. Am J Clin Pathol 139(3):345–349CrossRef
42.
go back to reference Aboian MS, Solomon DA, Felton E et al (2017) Imaging characteristics of pediatric diffuse midline gliomas with histone H3 K27M mutation. Am J Neuroradiol 38(4):795–800CrossRefPubMedPubMedCentral Aboian MS, Solomon DA, Felton E et al (2017) Imaging characteristics of pediatric diffuse midline gliomas with histone H3 K27M mutation. Am J Neuroradiol 38(4):795–800CrossRefPubMedPubMedCentral
43.
go back to reference Venneti S, Santi M, Felicella MM et al (2014) A sensitive and specific histopathologic prognostic marker for H3F3A K27M mutant pediatric glioblastomas. Acta Neuropathol 128(5):743–753CrossRefPubMedPubMedCentral Venneti S, Santi M, Felicella MM et al (2014) A sensitive and specific histopathologic prognostic marker for H3F3A K27M mutant pediatric glioblastomas. Acta Neuropathol 128(5):743–753CrossRefPubMedPubMedCentral
44.
go back to reference Reyes-Botero G, Giry M, Mokhtari K et al (2014) Molecular analysis of diffuse intrinsic brainstem gliomas in adults. J Neurooncol 116(2):405–411CrossRefPubMed Reyes-Botero G, Giry M, Mokhtari K et al (2014) Molecular analysis of diffuse intrinsic brainstem gliomas in adults. J Neurooncol 116(2):405–411CrossRefPubMed
47.
go back to reference Guillamo JS, Créange A, Kalifa C et al (2003) Prognostic factors of CNS tumours in neurofibromatosis 1 (NF1): a retrospective study of 104 patients. Brain 126(Pt 1):152–160CrossRefPubMed Guillamo JS, Créange A, Kalifa C et al (2003) Prognostic factors of CNS tumours in neurofibromatosis 1 (NF1): a retrospective study of 104 patients. Brain 126(Pt 1):152–160CrossRefPubMed
48.
49.
go back to reference Aihara K, Mukasa A, Gotoh K et al (2014) H3F3A K27M mutations in thalamic gliomas from young adult patients. Neuro-Oncology 16(1):140–146CrossRefPubMed Aihara K, Mukasa A, Gotoh K et al (2014) H3F3A K27M mutations in thalamic gliomas from young adult patients. Neuro-Oncology 16(1):140–146CrossRefPubMed
50.
go back to reference Ameratunga M, McArthur G, Gan H et al (2016) Prolonged disease control with MEK inhibitor in neurofibromatosis type I-associated glioblastoma. J Clin Pharm Ther 41(3):357–359CrossRefPubMed Ameratunga M, McArthur G, Gan H et al (2016) Prolonged disease control with MEK inhibitor in neurofibromatosis type I-associated glioblastoma. J Clin Pharm Ther 41(3):357–359CrossRefPubMed
51.
go back to reference Vanan MI, Underhill DA, Eisenstat DD (2017) Targeting epigenetic pathways in the treatment of pediatric Diffuse (high grade) gliomas. Neurotherapeutics 14(2):274–283CrossRefPubMed Vanan MI, Underhill DA, Eisenstat DD (2017) Targeting epigenetic pathways in the treatment of pediatric Diffuse (high grade) gliomas. Neurotherapeutics 14(2):274–283CrossRefPubMed
Metadata
Title
Characteristics of cerebellar glioblastomas in adults
Authors
Thiébaud Picart
Marc Barritault
Julien Berthillier
David Meyronet
Alexandre Vasiljevic
Didier Frappaz
Jérôme Honnorat
Emmanuel Jouanneau
Delphine Poncet
François Ducray
Jacques Guyotat
Publication date
01-02-2018
Publisher
Springer US
Published in
Journal of Neuro-Oncology / Issue 3/2018
Print ISSN: 0167-594X
Electronic ISSN: 1573-7373
DOI
https://doi.org/10.1007/s11060-017-2682-7

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