Contrast-enhancement in supratentorial low-grade gliomas: a classic prognostic factor in the molecular age

J Neurooncol. 2019 Jul;143(3):515-523. doi: 10.1007/s11060-019-03183-2. Epub 2019 May 3.

Abstract

Background: Contrast enhancement (CE) is found in 10-60% of low-grade gliomas. Its prognostic significance is controversial, and its correlation with IDH mutations and 1p/19q codeletion is elusive. The aim of this study is to investigate whether CE is associated with molecular characteristics of low-grade gliomas and uncover its prognostic value.

Materials and methods: All confirmed histological cases of low-grade gliomas diagnosed at our institution between years 2000-2016 were reviewed (n = 102). Spinal and brainstem localization, only-biopsied tumours with ring-like enhancement and incomplete medical records were excluded.

Results: Mean age was 42 years ( ± 13.9 years), and 63.6% were male. The median follow-up time was 79.8 months. CE was present on 25% of preoperative MRI, and 25% of patients were considered high-risk according to Pignatti score. Most were astrocytomas (67%) and 87.2% were surgically removed. IDH mutation was found in 64.6% of tumour samples, and 18.8% had a 1p/19q codeletion. No subgroup differences were observed according to CE except for presurgical performance status and postoperative chemotherapy. IDH status and 1p/19q codeletion were evenly distributed. On univariate analysis, age, size > 6 cm, CE, extent of resection, Pignatti score, IDH mutation and 1p/19q codeletion were significantly associated to OS. On multivariate analysis, only CE and IDH status were independently associated to OS. CE remained a significant prognostic factor in IDH-mutant non-codeleted tumours when analysed by tumour subtype.

Conclusion: CE in low-grade gliomas provides prognostic information in IDH-mutant non-codeleted tumours, although its meaning remains uncertain in IDH-wildtype gliomas.

Keywords: Astrocytoma; Contrast-enhancement; IDH; Low-grade glioma; Prognosis.

Publication types

  • Clinical Trial

MeSH terms

  • Adult
  • Biomarkers, Tumor / genetics
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 1 / genetics
  • Chromosomes, Human, Pair 19 / genetics
  • Combined Modality Therapy
  • Contrast Media*
  • Female
  • Follow-Up Studies
  • Glioma / genetics
  • Glioma / pathology*
  • Glioma / therapy
  • Humans
  • Image Enhancement / methods*
  • Isocitrate Dehydrogenase / genetics*
  • Magnetic Resonance Imaging
  • Male
  • Middle Aged
  • Mutation*
  • Neoplasm Grading
  • Survival Rate

Substances

  • Biomarkers, Tumor
  • Contrast Media
  • IDH2 protein, human
  • Isocitrate Dehydrogenase
  • IDH1 protein, human