Comparative molecular analysis of primary and recurrent oligodendroglioma that acquired imbalanced 1p/19q codeletion and TP53 mutation: a case report

Oligodendroglioma is defined by IDH mutation and 1p/19q codeletion. Normal TP53 status is also its molecular feature. We report a case of oligodendroglioma that acquired imbalanced 1p/19q codeletion and TP53 mutation at recurrence after temozolomide therapy. The primary and recurrent tumors shared I...

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Veröffentlicht in:Acta neurochirurgica 2020-12, Vol.162 (12), p.3019-3024
Hauptverfasser: Ono, Takahiro, Reinhardt, Annekathrin, Takahashi, Masataka, Nanjo, Hiroshi, Kamataki, Akihisa, von Deimling, Andreas, Shimizu, Hiroaki
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Sprache:eng
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Zusammenfassung:Oligodendroglioma is defined by IDH mutation and 1p/19q codeletion. Normal TP53 status is also its molecular feature. We report a case of oligodendroglioma that acquired imbalanced 1p/19q codeletion and TP53 mutation at recurrence after temozolomide therapy. The primary and recurrent tumors shared IDH1 and TERT promoter mutations. Although 1p/19q was codeleted in the primary tumor, it was imbalanced in the recurrent tumor harboring TP53 mutation. The copy-neutral loss of heterozygosity might have imbalanced the 1p/19q codeletion, while temozolomide therapy possibly caused the TP53 mutation. Such phenomena, although rare, should be noted during the clinical treatment of oligodendrogliomas.
ISSN:0001-6268
0942-0940
DOI:10.1007/s00701-020-04514-3