Isochromosome 17q is a negative prognostic factor in poor-risk childhood medulloblastoma patients

Edward Pan, Malgorzata Pellarin, Emi Holmes, Ivan Smirnov, Anjan Misra, Charles G. Eberhart, Peter C. Burger, Jaclyn A. Biegel, Burt G. Feuerstein, Shaun Mason

Research output: Contribution to journalArticlepeer-review

43 Scopus citations


Background: Medulloblastomas are the most common primary malignant childhood intracranial neoplasms. Patients are currently sorted into three risk groups based on clinical criteria: standard, poor, and infant (<18 months old). We hypothesized that genetic copy number aberrations (CNA) predict prognosis and would provide improved criteria for predicting outcome. Methods: DNA from 35 medulloblastoma patients from four Children's Cancer Group trials was analyzed by comparative genomic hybridization to determine CNAs. The genetic alterations were evaluated using statistical and cluster analyses. Rasults: The most frequent CNAs were gains on 17q, 7, 1q, and 7q and losses on 17p, 10q, X, 16q, and 11q. Amplification at 5p15.1-p15.3 was also detected. Isochromosome 17q (i(17)(q10)) was associated with poor overall survival (P = 0.03) and event-free survival (P = 0.04) independent of poor risk group classification. Age <3 tended to be associated with <3 CNAs (P = 0.06). Unsupervised cluster analysis sorted the study patients into four subgroups based on CNAs. Supervised analysis using the program Significance Analysis of Microarrays (SAM) quantitatively validated those CNAs identified by unsupervised clustering that significantly distinguished among the four subgroups. Conclusions: Medulloblastomas are genetically heterogeneous and can be categorized into separate genetic subgroups by their CNAs using unsupervised cluster analysis and SAM. i(17)(q10) was a significant independent negative prognostic factor. Infant medulloblastomas may be a distinct genetic subset from those of older patients.

Original languageEnglish (US)
Pages (from-to)4733-4740
Number of pages8
JournalClinical Cancer Research
Issue number13
StatePublished - Jul 1 2005

ASJC Scopus subject areas

  • Oncology
  • Cancer Research


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