TY - JOUR
T1 - Clinical and diffusion parameters may noninvasively predict TERT promoter mutation status in grade II meningiomas
AU - Shin, Ilah
AU - Park, Yae Won
AU - Ahn, Sung Soo
AU - Kang, Seok Gu
AU - Chang, Jong Hee
AU - Kim, Se Hoon
AU - Lee, Seung Koo
N1 - Publisher Copyright:
© 2021 Elsevier Masson SAS
PY - 2022/1
Y1 - 2022/1
N2 - Background and purpose: Increasing evidence suggests that genomic and molecular markers need to be integrated in grading of meningioma. Telomerase reverse transcriptase promoter (TERTp) mutation is receiving attention due to its clinical relevance in the treatment of meningiomas. The predictive ability of conventional and diffusion MRI parameters for determining the TERTp mutation status in grade II meningiomas has yet been identified. Material and methods: In this study, 63 patients with surgically confirmed grade II meningiomas (56 TERTp wildtype, 7 TERTp mutant) were included. Conventional imaging features were qualitatively assessed. The maximum diameter, volume of the tumors and histogram parameters from the apparent diffusion coefficient (ADC) were assessed. Independent clinical and imaging risk factors for TERTp mutation were investigated using multivariable logistic regression. The discriminative value of the prediction models with and without imaging features was evaluated. Results: In the univariable regression, older age (odds ratio [OR] = 1.13, P = 0.005), larger maximum diameter (OR = 1.09, P = 0.023), larger volume (OR = 1.04, P = 0.014), lower mean ADC (OR = 0.02, P = 0.025), and lower ADC 10th percentile (OR = 0.01, P = 0.014) were predictors of TERTp mutation. In multivariable regression, age (OR = 1.13, P = 0.009) and ADC 10th percentile (OR = 0.01, P = 0.038) were independent predictors of variables for predicting the TERTp mutation status. The performance of the prediction model increased upon inclusion of imaging parameters (area under the curves of 0.86 and 0.91, respectively, without and with imaging parameters). Conclusion: Older age and lower ADC 10th percentile may be useful parameters to predict TERTp mutation in grade II meningiomas.
AB - Background and purpose: Increasing evidence suggests that genomic and molecular markers need to be integrated in grading of meningioma. Telomerase reverse transcriptase promoter (TERTp) mutation is receiving attention due to its clinical relevance in the treatment of meningiomas. The predictive ability of conventional and diffusion MRI parameters for determining the TERTp mutation status in grade II meningiomas has yet been identified. Material and methods: In this study, 63 patients with surgically confirmed grade II meningiomas (56 TERTp wildtype, 7 TERTp mutant) were included. Conventional imaging features were qualitatively assessed. The maximum diameter, volume of the tumors and histogram parameters from the apparent diffusion coefficient (ADC) were assessed. Independent clinical and imaging risk factors for TERTp mutation were investigated using multivariable logistic regression. The discriminative value of the prediction models with and without imaging features was evaluated. Results: In the univariable regression, older age (odds ratio [OR] = 1.13, P = 0.005), larger maximum diameter (OR = 1.09, P = 0.023), larger volume (OR = 1.04, P = 0.014), lower mean ADC (OR = 0.02, P = 0.025), and lower ADC 10th percentile (OR = 0.01, P = 0.014) were predictors of TERTp mutation. In multivariable regression, age (OR = 1.13, P = 0.009) and ADC 10th percentile (OR = 0.01, P = 0.038) were independent predictors of variables for predicting the TERTp mutation status. The performance of the prediction model increased upon inclusion of imaging parameters (area under the curves of 0.86 and 0.91, respectively, without and with imaging parameters). Conclusion: Older age and lower ADC 10th percentile may be useful parameters to predict TERTp mutation in grade II meningiomas.
KW - Diffusion weighted imaging
KW - Magnetic resonance imaging
KW - Meningioma
KW - Radiogenomics
KW - Telomerase reverse transcriptase promoter gene
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U2 - 10.1016/j.neurad.2021.02.007
DO - 10.1016/j.neurad.2021.02.007
M3 - Article
C2 - 33716047
AN - SCOPUS:85102621051
SN - 0150-9861
VL - 49
SP - 59
EP - 65
JO - Journal of Neuroradiology
JF - Journal of Neuroradiology
IS - 1
ER -