Publication:
Outcome and prognostic factors in cerebellar glioblastoma multiforme in adults: A retrospective study from the rare cancer network

dc.contributor.authorsWeber, Damien C.; Miller, Robert C.; Villa, Salvador; Hanssens, Patrick; Baumert, Brigitta G.; Castadot, Pierre; Varlet, Pascale; Abacioglu, Ufuk; Igdem, Sefik; Szutowicz, Ewa; Nishioka, Hiroshi; Hofer, Silvia; Rutz, Hans Peter; Ozsahin, Mahmut; Taghian, Alphonse; Mirimanoff, Rene O.
dc.date.accessioned2022-03-12T17:32:09Z
dc.date.accessioned2026-01-11T11:07:26Z
dc.date.available2022-03-12T17:32:09Z
dc.date.issued2006
dc.description.abstractPurpose: The aim of this study was to assess the outcome in patients with cerebellar glioblastoma (GBM) treated in 15 institutions of the Rare Cancer Network. Methods and Materials: Data from a series of 45 adult patients with cerebellar GBM were collected in a retrospective multicenter study. Median age was 50.3 years. Brainstem invasion was observed in 9 (20%) patients. Radiotherapy (RT) was administered to 36 patients (with concomitant chemotherapy, 7 patients). Adjuvant chemotherapy after RT was administered in 8 patients. Median RT dose was 59.4 Gy. Median follow-up was 7.2 months (range, 3.4-39.0). Results: The 1-year and 2-year actuarial overall survival rate was 37.8% and 14.7%, respectively, and was significantly influenced by salvage treatment (p = 0.048), tumor volume (p = 0.044), extent of neurosurgical resection (p = 0.019), brainstem invasion (p = 0.0013), additional treatment after surgery (p < 0.001), and completion of the initial treatment (p < 0.001) on univariate analysis. All patients experienced local progression: 8 and 22 had progression with and without a distant failure, respectively. The 1- and 2-year actuarial progression free survival was 25% and 10.7%, respectively, and was significantly influenced by brainstem invasion (p = 0.002), additional treatment after surgery (p = 0.0016), and completion of the initial treatment (p < 0.001). On multivariate analysis, survival was negatively influenced by the extent of surgery (p = 0.03) and brainstem invasion (p = 0.02). Conclusions: In this multicenter retrospective study, the observed pattern of failure was local in all cases, but approximately 1 patient of 4 presented with an extracerebellar component. Brainstem invasion was observed in a substantial number of patients and was an adverse prognostic factor. (c) 2006 Elsevier Inc.
dc.identifier.doi10.1016/j.ijrobp.2006.04.035
dc.identifier.eissn1879-355X
dc.identifier.issn0360-3016
dc.identifier.pubmed16814953
dc.identifier.urihttps://hdl.handle.net/11424/228476
dc.identifier.wosWOS:000239931500023
dc.language.isoeng
dc.publisherELSEVIER SCIENCE INC
dc.relation.ispartofINTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectcerebellar glioblastoma
dc.subjectmalignant glioma
dc.subjectposterior fossa tumors
dc.subjectradiotherapy
dc.subjectchemotherapy
dc.subjectBRAIN-STEM GLIOMAS
dc.subjectPHASE-II
dc.subjectTEMOZOLOMIDE
dc.subjectRADIOTHERAPY
dc.subjectRADIATION
dc.subjectINFRATENTORIAL
dc.subjectASTROCYTOMAS
dc.subjectIRRADIATION
dc.subjectCHILDREN
dc.subjectTRIAL
dc.titleOutcome and prognostic factors in cerebellar glioblastoma multiforme in adults: A retrospective study from the rare cancer network
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage186
oaire.citation.issue1
oaire.citation.startPage179
oaire.citation.titleINTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS
oaire.citation.volume66

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