Academic Journal

Presence of an oligodendroglioma-like component in newly diagnosed glioblastoma identifies a pathogenetically heterogeneous subgroup and lacks prognostic value: central pathology review of the EORTC_26981/NCIC_CE.3 trial.

التفاصيل البيبلوغرافية
العنوان: Presence of an oligodendroglioma-like component in newly diagnosed glioblastoma identifies a pathogenetically heterogeneous subgroup and lacks prognostic value: central pathology review of the EORTC_26981/NCIC_CE.3 trial.
المؤلفون: Hegi, M.E., Janzer, R.C., Lambiv, W.L., Gorlia, T., Kouwenhoven, M.C., Hartmann, C., von Deimling, A., Martinet, D., Besuchet Schmutz, N., Diserens, A.C., Hamou, M.F., Bady, P., Weller, M., van den Bent, M.J., Mason, W.P., Mirimanoff, R.O., Stupp, R., Mokhtari, K., Wesseling, P., European Organisation for, Research, Treatment of Cancer Brain, Tumour
المساهمون: Radiation Oncology Groups, National Cancer Institute of Canada Clinical Trials Group, European Organisation for, Research, Treatment of Cancer Brain, Tumour
المصدر: Acta Neuropathologica, vol. 123, no. 6, pp. 841-852
سنة النشر: 2012
المجموعة: Université de Lausanne (UNIL): Serval - Serveur académique lausannois
مصطلحات موضوعية: Adolescent, Adult, Aged, Brain Neoplasms/genetics, Brain Neoplasms/pathology, Chemoradiotherapy, Clinical Trials, Phase III as Topic, DNA Methylation, Dacarbazine/analogs & derivatives, Dacarbazine/therapeutic use, Female, Glioblastoma/genetics, Glioblastoma/pathology, Humans, Male, Middle Aged, Mutation, Oligodendroglioma/genetics, Oligodendroglioma/pathology, Prognosis, Receptor, Epidermal Growth Factor/genetics, Epidermal Growth Factor/metabolism, Survival Analysis, Treatment Outcome, Young Adult
الوصف: Glioblastoma (GBM) is a morphologically heterogeneous tumor type with a median survival of only 15 months in clinical trial populations. However, survival varies greatly among patients. As part of a central pathology review, we addressed the question if patients with GBM displaying distinct morphologic features respond differently to combined chemo-radiotherapy with temozolomide. Morphologic features were systematically recorded for 360 cases with particular focus on the presence of an oligodendroglioma-like component and respective correlations with outcome and relevant molecular markers. GBM with an oligodendroglioma-like component (GBM-O) represented 15% of all confirmed GBM (52/339) and was not associated with a more favorable outcome. GBM-O encompassed a pathogenetically heterogeneous group, significantly enriched for IDH1 mutations (19 vs. 3%, p = 0.003) and EGFR amplifications (71 vs. 48%, p = 0.04) compared with other GBM, while co-deletion of 1p/19q was found in only one case and the MGMT methylation frequency was alike (47 vs. 46%). Expression profiles classified most of the GBM-O into two subtypes, 36% (5/14 evaluable) as proneural and 43% as classical GBM. The detection of pseudo-palisading necrosis (PPN) was associated with benefit from chemotherapy (p = 0.0002), while no such effect was present in the absence of PPN (p = 0.86). In the adjusted interaction model including clinical prognostic factors and MGMT status, PPN was borderline nonsignificant (p = 0.063). Taken together, recognition of an oligodendroglioma-like component in an otherwise classic GBM identifies a pathogenetically mixed group without prognostic significance. However, the presence of PPN may indicate biological features of clinical relevance for further improvement of therapy.
نوع الوثيقة: article in journal/newspaper
وصف الملف: application/pdf
اللغة: English
Relation: info:eu-repo/semantics/altIdentifier/pmid/22249618; info:eu-repo/semantics/altIdentifier/eissn/1432-0533; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_6613022C4BFB2; https://serval.unil.ch/notice/serval:BIB_6613022C4BFB; https://serval.unil.ch/resource/serval:BIB_6613022C4BFB.P001/REF.pdf
DOI: 10.1007/s00401-011-0938-4
الاتاحة: https://serval.unil.ch/notice/serval:BIB_6613022C4BFB
https://doi.org/10.1007/s00401-011-0938-4
https://serval.unil.ch/resource/serval:BIB_6613022C4BFB.P001/REF.pdf
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_6613022C4BFB2
Rights: info:eu-repo/semantics/openAccess ; Copying allowed only for non-profit organizations ; https://serval.unil.ch/disclaimer
رقم الانضمام: edsbas.F4B14AC6
قاعدة البيانات: BASE
الوصف
DOI:10.1007/s00401-011-0938-4