The impact of molecular and clinical factors on patient outcome in oligodendroglioma from 20 years’ experience at a single centre

Abstract The increased chemosensitivity of oligodendroglial tumours has been associated with loss of heterozygosity (LOH) of the p arm of chromosome 1 and the q arm of chromosome 19 (LOH 1p/19q). Other clinical and molecular factors have also been identified as being prognostic and predictive of tre...

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Published inJournal of clinical neuroscience Vol. 18; no. 3; pp. 329 - 333
Main Authors Parkinson, Jonathon F, Afaghi, Vahid, Payne, Cathy A, Buckland, Michael E, Brewer, Janice M, Biggs, Michael T, Little, Nicholas S, Wheeler, Helen R, Cook, Raymond J, McDonald, Kerrie L
Format Journal Article
LanguageEnglish
Published Scotland Elsevier Ltd 01.03.2011
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Summary:Abstract The increased chemosensitivity of oligodendroglial tumours has been associated with loss of heterozygosity (LOH) of the p arm of chromosome 1 and the q arm of chromosome 19 (LOH 1p/19q). Other clinical and molecular factors have also been identified as being prognostic and predictive of treatment outcome. We reviewed 105 patients with oligodendroglioma treated at a single centre over 20 years. Median survival in oligodendroglioma patients with LOH 1p/19q was significantly longer (10.9 vs . 2.0 years). In the anaplastic oligodendroglioma group, univariate analysis demonstrated decreased patient age, presentation with seizures, use of adjuvant chemotherapy and LOH 1p/19q as predictors of improved survival. Multivariate analysis confirmed LOH 1p/19q as a significant predictor of improved survival (hazard ratio, 3.4; p = 0.015). Median survival in patients with anaplastic oligodendroglioma with LOH 1p/19q was 15.4 years vs . 1.2 years for those without LOH 1p/19q. This study confirms the utility of LOH 1p/19q as a prognostic marker in oligodendroglioma.
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ISSN:0967-5868
1532-2653
DOI:10.1016/j.jocn.2010.07.101