| Literature DB >> 29980868 |
Shunichi Koriyama1,2, Masayuki Nitta3, Tatsuya Kobayashi1,2, Yoshihiro Muragaki1,2, Akane Suzuki4, Takashi Maruyama1,2, Takashi Komori5,6, Kenta Masui5, Taiichi Saito1,2, Takayuki Yasuda1,2, Junji Hosono1,2, Saori Okamoto1,2, Takahiro Shioyama4, Hiroaki Yamatani7, Takakazu Kawamata1.
Abstract
Lower grade gliomas are both treated and diagnosed via surgical resection. Maximum tumor resection is currently the standard of care; however, this risks the loss of brain function. Glioma can be genetically subdivided into three different types, based on isocitrate dehydrogenase (IDH) mutation status and the presence of 1p/19q codeletion, which have radically different prognoses and responses to adjuvant therapies. Therefore, the means to identify the subtype and evaluate the surrounding tissues during surgery would be advantageous. In this study, we have developed a new surgical strategy for lower grade glioma based on the fourth edition of the World Health Organization Brain Tumor Classification, involving intraoperative molecular diagnosis. High-resolution melting analysis was used to evaluate IDH mutational status, while rapid immunohistochemistry of p53 and alpha-thalassemia/mental retardation syndrome X-linked (ATRX) was used to evaluate the 1p/19q codeletion status, allowing genetic classification during surgery. In addition, intraoperative flow cytometry was used to evaluate the surgical cavity for additional tumor lesions, allowing maximal resection while mitigating the risk of functional losses. This strategy allows the rapid intraoperative diagnosis and mapping of lower grade gliomas, and its clinical use could dramatically improve its prognosis.Entities:
Keywords: Intraoperative flow cytometry; Intraoperative molecular diagnosis; Lower grade glioma; Surgical cavity diagnosis; Surgical strategy
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Year: 2018 PMID: 29980868 DOI: 10.1007/s10014-018-0324-1
Source DB: PubMed Journal: Brain Tumor Pathol ISSN: 1433-7398 Impact factor: 3.298