TY - JOUR
T1 - Magnetic Resonance Imaging Parameters for Noninvasive Prediction of Epidermal Growth Factor Receptor Amplification in Isocitrate Dehydrogenase-Wild-Type Lower-Grade Gliomas
T2 - A Multicenter Study
AU - Park, Yae Won
AU - Park, Ji Eun
AU - Ahn, Sung Soo
AU - Kim, Eui Hyun
AU - Kang, Seok Gu
AU - Chang, Jong Hee
AU - Kim, Se Hoon
AU - Choi, Seung Hong
AU - Kim, Ho Sung
AU - Lee, Seung Koo
N1 - Publisher Copyright:
© 2021 Congress of Neurological Surgeons.
PY - 2021/8/1
Y1 - 2021/8/1
N2 - BACKGROUND: The epidermal growth factor receptor (EGFR) amplification status of isocitrate dehydrogenase-wild-type (IDHwt) lower-grade gliomas (LGGs; grade II/III) is one of the key markers for diagnosing molecular glioblastoma. However, the association between EGFR status and imaging parameters is unclear. OBJECTIVE: To identify noninvasive imaging parameters from diffusion-weighted and dynamic susceptibility contrast imaging for predicting the EGFR amplification status of IDHwt LGGs. METHODS: A total of 86 IDHwt LGG patients with known EGFR amplification status (62 nonamplified and 24 amplified) from 3 tertiary institutions were included. Qualitative and quantitative imaging features, including histogram parameters from apparent diffusion coefficient (ADC), normalized cerebral blood volume (nCBV), and normalized cerebral blood flow (nCBF), were assessed. Univariable and multivariable logistic regression models were constructed. RESULTS: On multivariable analysis, multifocal/multicentric distribution (odds ratio [OR] = 11.77, P =. 006), mean ADC (OR = 0.01, P =. 044), 5th percentile of ADC (OR = 0.01, P =. 046), and 95th percentile of nCBF (OR = 1.24, P =. 031) were independent predictors of EGFR amplification. The diagnostic performance of the model with qualitative imaging parameters increased significantly when quantitative imaging parameters were added, with areas under the curves of 0.81 and 0.93, respectively (P =. 004). CONCLUSION: The presence of multifocal/multicentric distribution patterns, lower mean ADC, lower 5th percentile of ADC, and higher 95th percentile of nCBF may be useful imaging biomarkers for EGFR amplification in IDHwt LGGs. Moreover, quantitative imaging biomarkers may add value to qualitative imaging parameters.
AB - BACKGROUND: The epidermal growth factor receptor (EGFR) amplification status of isocitrate dehydrogenase-wild-type (IDHwt) lower-grade gliomas (LGGs; grade II/III) is one of the key markers for diagnosing molecular glioblastoma. However, the association between EGFR status and imaging parameters is unclear. OBJECTIVE: To identify noninvasive imaging parameters from diffusion-weighted and dynamic susceptibility contrast imaging for predicting the EGFR amplification status of IDHwt LGGs. METHODS: A total of 86 IDHwt LGG patients with known EGFR amplification status (62 nonamplified and 24 amplified) from 3 tertiary institutions were included. Qualitative and quantitative imaging features, including histogram parameters from apparent diffusion coefficient (ADC), normalized cerebral blood volume (nCBV), and normalized cerebral blood flow (nCBF), were assessed. Univariable and multivariable logistic regression models were constructed. RESULTS: On multivariable analysis, multifocal/multicentric distribution (odds ratio [OR] = 11.77, P =. 006), mean ADC (OR = 0.01, P =. 044), 5th percentile of ADC (OR = 0.01, P =. 046), and 95th percentile of nCBF (OR = 1.24, P =. 031) were independent predictors of EGFR amplification. The diagnostic performance of the model with qualitative imaging parameters increased significantly when quantitative imaging parameters were added, with areas under the curves of 0.81 and 0.93, respectively (P =. 004). CONCLUSION: The presence of multifocal/multicentric distribution patterns, lower mean ADC, lower 5th percentile of ADC, and higher 95th percentile of nCBF may be useful imaging biomarkers for EGFR amplification in IDHwt LGGs. Moreover, quantitative imaging biomarkers may add value to qualitative imaging parameters.
UR - http://www.scopus.com/inward/record.url?scp=85112125509&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85112125509&partnerID=8YFLogxK
U2 - 10.1093/neuros/nyab136
DO - 10.1093/neuros/nyab136
M3 - Article
C2 - 33913501
AN - SCOPUS:85112125509
SN - 0148-396X
VL - 89
SP - 257
EP - 265
JO - Neurosurgery
JF - Neurosurgery
IS - 2
ER -