Abstract
The characteristics of hydrocephalus associated with cerebellar glioblastoma (cGB) remain poorly known. The objectives were to describe the occurence of hydrocephalus in a French nationwide series of adult patients with cGB, to identify the characteristics associated with hydrocephalus and to analyze the outcomes associated with the different surgical strategies, in order to propose practical guidelines. Consecutive cases of adult cGB patients prospectively recorded into the French Brain Tumor Database between 2003 and 2017 were screened. Diagnosis was confirmed by a centralized neuropathological review. Among 118 patients with cGB (mean age 55.9 years), 49 patients (41.5%) presented with pre-operative hydrocephalus. Thirteen patients (11.0%) developed acute (n=7) or delayed (n=6) hydrocephalus postoperatively. Compared to patients without hydrocephalus at admission, patients with hydrocephalus were younger (52.0 years vs 58.6 years, p=0.03) and underwent more frequently tumor resection (93.9% vs 73.9%, p=0.006). A total of 40 cerebrospinal-fluid diversion procedures were performed, including 18 endoscopic third ventriculostomies, 12 ventriculoperitoneal shunts and 10 external ventricular drains. The different cerebrospinal-fluid diversion options had comparable functional results and complication rates. Among the 89 patients surgically managed for cGB without prior cerebrospinal-fluid diversion, 7 (7.9%) were long-term shunt-dependant. Hydrocephalus is frequent in patients with cGB and has to be carefully managed in order not to interfere with adjuvant oncological treatments. In case of symptomatic hydrocephalus, a cerebrospinal-fluid diversion is mandatory, especially if surgical resection is not feasible. In case of asymptomatic hydrocephalus, a cerebrospinal-fluid diversion has to be discussed only if surgical resection is not feasible.
Similar content being viewed by others
References
Atlas MD, Perez de Tagle JR, Cook JA, Sheehy JP, Fagan PA (1996) Evolution of the management of hydrocephalus associated with acoustic neuroma. Laryngoscope 106:204–206. https://doi.org/10.1097/00005537-199602000-00018
Briggs RJ, Shelton C, Kwartler JA, Hitselberger W (1993) Management of hydrocephalus resulting from acoustic neuromas. Otolaryngol Head Neck Surg 109:1020–1024. https://doi.org/10.1177/019459989310900608
Chan AW, Tarbell NJ, Black PM, Louis DN, Frosch MP, Ancukiewicz M, Chapman P, Loeffler JS (2000) Adult medulloblastoma: prognostic factors and patterns of relapse. Neurosurgery 47:623–631; discussion 631-632. https://doi.org/10.1097/00006123-200009000-00018
Marx S, Damaty AE, Manwaring J, Refaee EE, Fleck S, Fritsch M, Gaab MR, Schroeder HWS, Baldauf J (2018) Endoscopic Third Ventriculostomy before Posterior Fossa Tumor Surgery in Adult Patients. J Neurol Surg A Cent Eur Neurosurg 79:123–129. https://doi.org/10.1055/s-0037-1608786
Roux A, Botella C, Still M, Zanello M, Dhermain F, Metellus P, Pallud J (2018) Posterior Fossa Metastasis-Associated Obstructive Hydrocephalus in Adult Patients: Literature Review and Practical Considerations from the Neuro-Oncology Club of the French Society of Neurosurgery. World Neurosurg 117:271–279. https://doi.org/10.1016/j.wneu.2018.06.084
Lee SH, Kong DS, Seol HJ, Nam D-H, Lee J-I (2011) Ventriculoperitoneal shunt for hydrocephalus caused by central nervous system metastasis. J Neuro-Oncol 104:545–551. https://doi.org/10.1007/s11060-010-0512-2
Mangubat EZ, Chan M, Ruland S, Roitberg BZ (2009) Hydrocephalus in posterior fossa lesions: ventriculostomy and permanent shunt rates by diagnosis. Neurol Res 31:668–673. https://doi.org/10.1179/174313209X380937
Marx S, Reinfelder M, Matthes M, Schroeder HWS, Baldauf J (2018) Frequency and treatment of hydrocephalus prior to and after posterior fossa tumor surgery in adult patients. Acta Neurochir 160:1063–1071. https://doi.org/10.1007/s00701-018-3496-x
Adams H, Chaichana KL, Avendaño J, Liu B, Raza SM, Quiñones-Hinojosa A (2013) Adult cerebellar glioblastoma: understanding survival and prognostic factors using a population-based database from 1973 to 2009. World Neurosurg 80:e237–e243. https://doi.org/10.1016/j.wneu.2013.02.010
Babu R, Sharma R, Karikari IO, Owens TR, Friedman AH, Adamson C (2013) Outcome and prognostic factors in adult cerebellar glioblastoma. J Clin Neurosci 20:1117–1121. https://doi.org/10.1016/j.jocn.2012.12.006
Jeswani S, Nuño M, Folkerts V, Mukherjee D, Black KL, Patil CG (2013) Comparison of survival between cerebellar and supratentorial glioblastoma patients: surveillance, epidemiology, and end results (SEER) analysis. Neurosurgery 73:240–246; discussion 246; quiz 246. https://doi.org/10.1227/01.neu.0000430288.85680.37
Picart T, Barritault M, Berthillier J, Meyronet D, Vasiljevic A, Frappaz D, Honnorat J, Jouanneau E, Poncet D, Ducray F, Guyotat J (2018) Characteristics of cerebellar glioblastomas in adults. J Neuro-Oncol 136:555–563. https://doi.org/10.1007/s11060-017-2682-7
Stark AM, Maslehaty H, Hugo HH, Mahvash M, Mehdorn HM (2010) Glioblastoma of the cerebellum and brainstem. J Clin Neurosci 17:1248–1251. https://doi.org/10.1016/j.jocn.2010.02.015
Takahashi Y, Makino K, Nakamura H, Hide T, Yano S, Kamada H, Kuratsu J-I (2014) Clinical characteristics and pathogenesis of cerebellar glioblastoma. Mol Med Rep 10:2383–2388. https://doi.org/10.3892/mmr.2014.2549
Picart T, Meyronet D, Pallud J, Dumot C, Metellus P, Zouaoui S, Berhouma M, Ducray F, Bauchet L, Guyotat J, French Brain Tumor DataBase, Club de Neuro-Oncologie of the Société Française de Neurochirurgie (2021) Management, functional outcomes and survival in a French multicentric series of 118 adult patients with cerebellar glioblastoma. J Cancer Res Clin Oncol 147:1843–1856. https://doi.org/10.1007/s00432-020-03474-6
Darlix A, Zouaoui S, Rigau V, Bessaoud F, Figarella-Branger D, Mathieu-Daudé H, Trétarre B, Bauchet F, Duffau H, Taillandier L, Bauchet L (2017) Epidemiology for primary brain tumors: a nationwide population-based study. J Neuro-Oncol 131:525–546. https://doi.org/10.1007/s11060-016-2318-3
Ng S, Zouaoui S, Bessaoud F, Rigau V, Roux A, Darlix A, Bauchet F, Mathieu-Daudé H, Trétarre B, Figarella-Branger D, Pallud J, Frappaz D, Roujeau T, Bauchet L (2019) An Epidemiology Report for Primary Central Nervous System Tumors in Adolescents and Young Adults: a nationwide population-based study in France, 2008-2013. Neuro-oncology. 22:851–863. https://doi.org/10.1093/neuonc/noz227
Rigau V, Zouaoui S, Mathieu-Daudé H, Darlix A, Maran A, Trétarre B, Bessaoud F, Bauchet F, Attaoua R, Fabbro-Peray P, Fabbro M, Kerr C, Taillandier L, Duffau H, Figarella-Branger D, Costes V, Bauchet L, Société Française de Neuropathologie (SFNP), Société Française de Neurochirurgie (SFNC), Club de Neuro-Oncologie of the Société Française de Neurochirurgie (CNO-SFNC), Association des Neuro-Oncologues d’Expression Française (ANOCEF) (2011) French brain tumor database: 5-year histological results on 25 756 cases. Brain Pathol 21:633–644. https://doi.org/10.1111/j.1750-3639.2011.00491.x
Zouaoui S, Rigau V, Mathieu-Daudé H, Darlix A, Bessaoud F, Fabbro-Peray P, Bauchet F, Kerr C, Fabbro M, Figarella-Branger D, Taillandier L, Duffau H, Trétarre B, Bauchet L, Société française de neurochirurgie (SFNC) et le Club de neuro-oncologie de la SFNC, Société française de neuropathologie (SFNP), Association des neuro-oncologues d’expression française (ANOCEF) (2012) French brain tumor database: general results on 40,000 cases, main current applications and future prospects. Neurochirurgie 58:4–13. https://doi.org/10.1016/j.neuchi.2012.01.004
Wen PY, Macdonald DR, Reardon DA, Cloughesy TF, Sorensen AG, Galanis E, Degroot J, Wick W, Gilbert MR, Lassman AB, Tsien C, Mikkelsen T, Wong ET, Chamberlain MC, Stupp R, Lamborn KR, Vogelbaum MA, van den Bent MJ, Chang SM (2010) Updated response assessment criteria for high-grade gliomas: response assessment in neuro-oncology working group. J Clin Oncol 28:1963–1972. https://doi.org/10.1200/JCO.2009.26.3541
Louis DN, Perry A, Reifenberger G, von Deimling A, Figarella-Branger D, Cavenee WK, Ohgaki H, Wiestler OD, Kleihues P, Ellison DW (2016) The 2016 World Health Organization Classification of Tumors of the Central Nervous System: a summary. Acta Neuropathol 131:803–820. https://doi.org/10.1007/s00401-016-1545-1
Kuroiwa T, Numaguchi Y, Rothman MI, Zoarski GH, Morikawa M, Zagardo MT, Kristt DA (1995) Posterior fossa glioblastoma multiforme: MR findings. AJNR Am J Neuroradiol 16:583–589
Fukuda M, Oishi M, Kawaguchi T, Watanabe M, Takao T, Tanaka R, Fujii Y (2007) Etiopathological factors related to hydrocephalus associated with vestibular schwannoma. Neurosurgery 61:1186–1192; discussion 1192-1193. https://doi.org/10.1227/01.neu.0000306096.61012.22
Gerganov VM, Pirayesh A, Nouri M, Hore N, Luedemann WO, Oi S, Samii A, Samii M (2011) Hydrocephalus associated with vestibular schwannomas: management options and factors predicting the outcome. J Neurosurg 114:1209–1215. https://doi.org/10.3171/2010.10.JNS1029
Harati A, Scheufler K-M, Schultheiss R, Tonkal A, Harati K, Oni P, Deitmer T (2017) Clinical features, microsurgical treatment, and outcome of vestibular schwannoma with brainstem compression. Surg Neurol Int 8:45. https://doi.org/10.4103/sni.sni_129_16
Miyakoshi A, Kohno M, Nagata O, Sora S, Sato H (2013) Hydrocephalus associated with vestibular schwannomas: perioperative changes in cerebrospinal fluid. Acta Neurochir 155:1271–1276. https://doi.org/10.1007/s00701-013-1742-9
Rogg JM, Ahn SH, Tung GA, Reinert SE, Norén G (2005) Prevalence of hydrocephalus in 157 patients with vestibular schwannoma. Neuroradiology 47:344–351. https://doi.org/10.1007/s00234-005-1363-y
di Russo P, Fava A, Vandenbulcke A, Miyakoshi A, Kohno M, Evins AI, Esposito V, Morace R (2020) Characteristics and management of hydrocephalus associated with vestibular schwannomas: a systematic review. Neurosurg Rev 44:687–698. https://doi.org/10.1007/s10143-020-01287-2
Pirouzmand F, Tator CH, Rutka J (2001) Management of hydrocephalus associated with vestibular schwannoma and other cerebellopontine angle tumors. Neurosurgery 48:1246–1253; discussion 1253-1254. https://doi.org/10.1097/00006123-200106000-00010
Ghani E, Zaidi GI, Nadeem M, Rehman L, Noman MA, Khaleeq-Uz-Zaman null (2003) Role of cerebrospinal fluid diversion in posterior fossa tumor surgery. J Coll Physicians Surg Pak 13:333–336. doi: 06.2003/JCPSP.333336
Sunderland GJ, Jenkinson MD, Zakaria R (2016) Surgical management of posterior fossa metastases. J Neuro-Oncol 130:535–542. https://doi.org/10.1007/s11060-016-2254-2
Taylor WA, Todd NV, Leighton SE (1992) CSF drainage in patients with posterior fossa tumours. Acta Neurochir 117:1–6. https://doi.org/10.1007/bf01400627
El-Gaidi MA, El-Nasr AHA, Eissa EM (2015) Infratentorial complications following preresection CSF diversion in children with posterior fossa tumors. J Neurosurg Pediatr 15:4–11. https://doi.org/10.3171/2014.8.PEDS14146
Bloch J, Vernet O, Aubé M, Villemure J-G (2003) Non-obstructive hydrocephalus associated with intracranial schwannomas: hyperproteinorrhachia as an etiopathological factor? Acta Neurochir 145:73–78. https://doi.org/10.1007/s00701-002-1021-7
Hong B, Polemikos M, Heissler HE, Hartmann C, Nakamura M, Krauss JK (2018) Challenges in cerebrospinal fluid shunting in patients with glioblastoma. Fluids Barriers CNS 15:16. https://doi.org/10.1186/s12987-018-0101-x
Ferguson SD, Xiu J, Weathers S-P, Zhou S, Kesari S, Weiss SE, Verhaak RG, Hohl RJ, Barger GR, Reddy SK, Heimberger AB (2016) GBM-associated mutations and altered protein expression are more common in young patients. Oncotarget 7:69466–69478. https://doi.org/10.18632/oncotarget.11617
Meyronet D, Esteban-Mader M, Bonnet C, Joly M-O, Uro-Coste E, Amiel-Benouaich A, Forest F, Rousselot-Denis C, Burel-Vandenbos F, Bourg V, Guyotat J, Fenouil T, Jouvet A, Honnorat J, Ducray F (2017) Characteristics of H3 K27M-mutant gliomas in adults. Neuro-oncology 19:1127–1134. https://doi.org/10.1093/neuonc/now274
Izquierdo C, Barritault M, Poncet D, Cartalat S, Joubert B, Bruna J, Jouanneau E, Guyotat J, Vasiljevic A, Fenouil T, Berthezène Y, Honnorat J, Meyronet D, Ducray F (2019) Radiological Characteristics and Natural History of Adult IDH-Wildtype Astrocytomas with TERT Promoter Mutations. Neurosurgery 85:E448–E456. https://doi.org/10.1093/neuros/nyy513
Di Carlo DT, Cagnazzo F, Benedetto N, Morganti R, Perrini P (2019) Multiple high-grade gliomas: epidemiology, management, and outcome. A systematic review and meta-analysis. Neurosurg Rev 42:263–275. https://doi.org/10.1007/s10143-017-0928-7
Weber DC, Miller RC, Villà S, Hanssens P, Baumert BG, Castadot P, Varlet P, Abacioglu U, Igdem S, Szutowicz E, Nishioka H, Hofer S, Rutz HP, Ozsahin M, Taghian A, Mirimanoff RO (2006) Outcome and prognostic factors in cerebellar glioblastoma multiforme in adults: a retrospective study from the Rare Cancer Network. Int J Radiat Oncol Biol Phys 66:179–186. https://doi.org/10.1016/j.ijrobp.2006.04.035
Won S-Y, Dubinski D, Behmanesh B, Bernstock JD, Seifert V, Konczalla J, Tritt S, Senft C, Gessler F (2019) Management of hydrocephalus after resection of posterior fossa lesions in pediatric and adult patients-predictors for development of hydrocephalus. Neurosurg Rev 43:1143–1150. https://doi.org/10.1007/s10143-019-01139-8
Won S-Y, Gessler F, Dubinski D, Eibach M, Behmanesh B, Herrmann E, Seifert V, Konczalla J, Tritt S, Senft C (2019) A novel grading system for the prediction of the need for cerebrospinal fluid drainage following posterior fossa tumor surgery. J Neurosurg 132:296–305. https://doi.org/10.3171/2018.8.JNS181005
Reddy GK, Bollam P, Caldito G, Willis B, Guthikonda B, Nanda A (2011) Ventriculoperitoneal shunt complications in hydrocephalus patients with intracranial tumors: an analysis of relevant risk factors. J Neuro-Oncol 103:333–342. https://doi.org/10.1007/s11060-010-0393-4
Chen CC, Kasper E, Warnke P (2011) Palliative stereotactic-endoscopic third ventriculostomy for the treatment of obstructive hydrocephalus from cerebral metastasis. Surg Neurol Int 2:76. https://doi.org/10.4103/2152-7806.82083
Gonda DD, Kim TE, Warnke PC, Kasper EM, Carter BS, Chen CC (2012) Ventriculoperitoneal shunting versus endoscopic third ventriculostomy in the treatment of patients with hydrocephalus related to metastasis. Surg Neurol Int 3:97. https://doi.org/10.4103/2152-7806.100185
Di Vincenzo J, Keiner D, Gaab MR, Schroeder HWS, Oertel JMK (2014) Endoscopic third ventriculostomy: preoperative considerations and intraoperative strategy based on 300 procedures. J Neurol Surg A Cent Eur Neurosurg 75:20–30. https://doi.org/10.1055/s-0032-1328953
Grand W, Leonardo J, Chamczuk AJ, Korus AJ (2016) Endoscopic Third Ventriculostomy in 250 Adults With Hydrocephalus: Patient Selection, Outcomes, and Complications. Neurosurgery 78:109–119. https://doi.org/10.1227/NEU.0000000000000994
Isaacs AM, Bezchlibnyk YB, Yong H, Koshy D, Urbaneja G, Hader WJ, Hamilton MG (2016) Endoscopic third ventriculostomy for treatment of adult hydrocephalus: long-term follow-up of 163 patients. Neurosurg Focus 41:E3. https://doi.org/10.3171/2016.6.FOCUS16193
Acknowledgements
We thank all contributors from the French Brain Tumor Database and from the Club de Neuro-Oncologie of the Société Française de Neurochirurgie and Mr Julien Berthiller, biostatistician. Moreover, we thank the non-profit organizations that support the FBTDB: Ligue Nationale Contre le Cancer and comité 34, Associations pour la Recherche sur les Tumeurs Cérébrales (ARTC) Nord et Sud, Des étoiles dans la Mer ; as well as the French Glioblastoma biobank (FGB) and the French Institut National du Cancer-INCa.
Data Availability (data transparency)
Anonymized data will be shared by request from any qualified investigator.
Code availability
Not applicable
Funding
No funding was received for conducting this study.
Author information
Authors and Affiliations
Consortia
Contributions
Thiébaud Picart, Luc Bauchet and Jacques Guyotat designed and conceptualized the study.
Thiébaud Picart, Chloé Dumot, David Meyronet, Johan Pallud, Philippe Metellus, Sonia Zouaoui, François Ducray, Isabelle Pelissou-Guyotat, Moncef Berhouma and all members from the French Brain Tumor DataBase and the Club de Neuro-Oncologie of the Société Française de Neurochirurgie had a major role in the acquisition of data.
Thiébaud Picart and David Meyronet analyzed and interpreted the data.
Thiébaud Picart, Luc Bauchet and Jacques Guyotat drafted the manuscript.
All authors critically revised the manuscript for intellectual content and approved the final version.
Corresponding author
Ethics declarations
Ethics approval
This study was performed in line with the principles of the Declaration of Helsinki. Approval was granted by the French legislation (CCTIRS n°10.548; CNIL n°911013).
Consent to participate (include appropriate statements)
All patients provided written informed consent for study inclusion.
Consent for publication (include appropriate statements)
All living patients provided written informed consent for data publication.
Conflicts of interest
Drs. Thiébaud Picart, Chloé Dumot, David Meyronet, Johan Pallud, Philippe Metellus, Sonia Zouaoui, François Ducray, Isabelle Pelissou-Guyotat, Moncef Berhouma, Luc Bauchet, Jacques Guyotat, all members of the French Brain Tumor DataBase and Club de Neuro-Oncologie of the Société Française de Neurochirurgie declare that they have no conflict of interest.
Additional information
Publisher’s note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
About this article
Cite this article
Picart, T., Dumot, C., Meyronet, D. et al. Characteristics and management of hydrocephalus in adult patients with cerebellar glioblastoma: lessons from a French nationwide series of 118 cases. Neurosurg Rev 45, 683–699 (2022). https://doi.org/10.1007/s10143-021-01578-2
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s10143-021-01578-2