TY - JOUR
T1 - Reliability of IDH1-R132H and ATRX and/or p53 immunohistochemistry for molecular subclassification of Grade 2/3 gliomas
AU - Nishikawa, Tomohide
AU - Watanabe, Reiko
AU - Kitano, Yotaro
AU - Yamamichi, Akane
AU - Motomura, Kazuya
AU - Ohka, Fumiharu
AU - Aoki, Kosuke
AU - Hirano, Masaki
AU - Kato, Akira
AU - Yamaguchi, Junya
AU - Maeda, Sachi
AU - Kibe, Yuji
AU - Saito, Ryuta
AU - Wakabayashi, Toshihiko
AU - Kato, Yukinari
AU - Sato, Shuta
AU - Ogino, Tomoyoshi
AU - Natsume, Atsushi
AU - Ito, Ichiro
N1 - Funding Information:
This research was supported by a Grant-in-Aid for Scientific Research on Innovative Areas “Chemistry for Multimolecular Crowding Biosystems” (A.N.) (JSPS KAKENHI Grant No. 17928985). This research was also supported in part by the Japan Agency for Medical Research and Development (AMED) under Grant Number: JP21am0101078 (to Y.K.).
Publisher Copyright:
© 2021, The Author(s) under exclusive licence to The Japan Society of Brain Tumor Pathology.
PY - 2022/1
Y1 - 2022/1
N2 - Since the World Health Organization 2016 classification (2016 WHO), genetic status has been incorporated into the diagnosis of Grade 2/3 gliomas (lower-grade gliomas). Therefore, immunohistochemistry (IHC) of IDH1-R132H, ATRX, and p53 have been used in place of genetic status. We report the associations between histological findings, IHC, and genetic status. We performed IHC of IDH1-R132H, ATRX, and p53 in 76 lower-grade gliomas and discussed its validity based on the 2016 WHO and the upcoming 2021 WHO classification. The sensitivity and specificity of anti-ATRX, p53, and IDH1-R132H IHC were 40.9%/98.1%, 78.6%/85.4%, and 90.5%/84.6%, respectively. Among 21 IDH1-mutant gliomas without 1p/19q codeletion, two gliomas (9.5%) mimicked the so-called classic for oligodendroglioma (CFO) in their morphology. Of the 42 gliomas with 1p/19q codeletion, four cases were difficult to diagnose as oligodendroglioma through morphological examination. Moreover, there were three confusing cases with ATRX mutations but with retained ATRX-IHC positivity. The lessons learned from this study are as follows: (1) ATRX-IHC and p53-IHC should be supplementary to morphological diagnosis, (2) rare IDH mutations other than IDH1 R132H should be considered, and (3) there is no complete alternative test to detect molecular features of glioblastoma under the 2021 WHO classification.
AB - Since the World Health Organization 2016 classification (2016 WHO), genetic status has been incorporated into the diagnosis of Grade 2/3 gliomas (lower-grade gliomas). Therefore, immunohistochemistry (IHC) of IDH1-R132H, ATRX, and p53 have been used in place of genetic status. We report the associations between histological findings, IHC, and genetic status. We performed IHC of IDH1-R132H, ATRX, and p53 in 76 lower-grade gliomas and discussed its validity based on the 2016 WHO and the upcoming 2021 WHO classification. The sensitivity and specificity of anti-ATRX, p53, and IDH1-R132H IHC were 40.9%/98.1%, 78.6%/85.4%, and 90.5%/84.6%, respectively. Among 21 IDH1-mutant gliomas without 1p/19q codeletion, two gliomas (9.5%) mimicked the so-called classic for oligodendroglioma (CFO) in their morphology. Of the 42 gliomas with 1p/19q codeletion, four cases were difficult to diagnose as oligodendroglioma through morphological examination. Moreover, there were three confusing cases with ATRX mutations but with retained ATRX-IHC positivity. The lessons learned from this study are as follows: (1) ATRX-IHC and p53-IHC should be supplementary to morphological diagnosis, (2) rare IDH mutations other than IDH1 R132H should be considered, and (3) there is no complete alternative test to detect molecular features of glioblastoma under the 2021 WHO classification.
KW - ATRX
KW - Genetics
KW - Glioma
KW - Immunohistochemistry
KW - Surrogate marker
KW - WHO 5th CNS tumor classification 2021
KW - p53
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U2 - 10.1007/s10014-021-00418-x
DO - 10.1007/s10014-021-00418-x
M3 - Article
C2 - 34826036
AN - SCOPUS:85120000759
SN - 1433-7398
VL - 39
SP - 14
EP - 24
JO - Brain Tumor Pathology
JF - Brain Tumor Pathology
IS - 1
ER -