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Association of ADC of hyperintense lesions on FLAIR images with TERT promoter mutation status in glioblastoma IDH wild type.
Kamimura, Shigeru; Mitobe, Yuta; Nakamura, Kazuki; Matsuda, Kenichiro; Kanemura, Yonehiro; Kanoto, Masafumi; Futakuchi, Mitsuru; Sonoda, Yukihiko.
Afiliación
  • Kamimura S; Department of Neurosurgery, Yamagata University, Yamagata, Japan.
  • Mitobe Y; Department of Neurosurgery, Yamagata University, Yamagata, Japan.
  • Nakamura K; Department of Neurosurgery, Yamagata University, Yamagata, Japan.
  • Matsuda K; Department of Neurosurgery, Yamagata University, Yamagata, Japan.
  • Kanemura Y; Department of Biomedical Research and Innovation, National Hospital Organization Osaka National Hospital, Osaka, Japan.
  • Kanoto M; Department of Radiology, Division of Diagnostic Radiology, Yamagata University, Yamagata, Japan.
  • Futakuchi M; Department of Pathological Diagnostics, Yamagata University, Yamagata, Japan.
  • Sonoda Y; Department of Neurosurgery, Yamagata University, Yamagata, Japan.
Surg Neurol Int ; 15: 108, 2024.
Article en En | MEDLINE | ID: mdl-38628517
ABSTRACT

Background:

Although mutations in telomerase reverse transcriptase (TERT) promoter (TERTp) are the most common alterations in glioblastoma (GBM), predicting TERTp mutation status by preoperative imaging is difficult. We determined whether tumour-surrounding hyperintense lesions on fluid-attenuated inversion recovery (FLAIR) were superior to those of contrast-enhanced lesions (CELs) in assessing TERTp mutation status using magnetic resonance imaging (MRI).

Methods:

This retrospective study included 114 consecutive patients with primary isocitrate dehydrogenase (IDH)-wild-type GBM. The apparent diffusion coefficient (ADC) and volume of CELs and FLAIR hyperintense lesions (FHLs) were determined, and the correlation between MRI features and TERTp mutation status was analyzed. In a subset of cases, FHLs were histopathologically analyzed to determine the correlation between tumor cell density and ADC.

Results:

TERTp mutations were present in 77 (67.5%) patients. The minimum ADC of FHLs was significantly lower in the TERTp-mutant group than in the TERTp-wild-type group (mean, 958.9 × 10-3 and 1092.1 × 10-3 mm2/s, respectively, P < 0.01). However, other MRI features, such as CEL and FHL volumes, minimum ADC of CELs, and FHL/CEL ratio, were not significantly different between the two groups. Histopathologic analysis indicated high tumor cell density in FHLs with low ADC.

Conclusion:

The ADC of FHLs was significantly lower in IDH-wild-type GBM with TERTp mutations, suggesting that determining the ADC of FHLs on preoperative MRI might be helpful in predicting TERTp mutation status and surgical planning.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Surg Neurol Int Año: 2024 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Surg Neurol Int Año: 2024 Tipo del documento: Article País de afiliación: Japón