| Literature DB >> 26181761 |
Ganesh M Shankar1, Joshua M Francis2, Mikael L Rinne3, Shakti H Ramkissoon4, Franklin W Huang2, Andrew S Venteicher5, Elliot H Akama-Garren6, Yun Jee Kang7, Nina Lelic8, James C Kim9, Loreal E Brown7, Sarah K Charbonneau7, Alexandra J Golby10, Chandra Sekhar Pedamallu2, Mai P Hoang9, Ryan J Sullivan11, Andrew D Cherniack12, Levi A Garraway2, Anat Stemmer-Rachamimov9, David A Reardon13, Patrick Y Wen14, Priscilla K Brastianos11, William T Curry8, Fred G Barker8, William C Hahn2, Brian V Nahed8, Keith L Ligon15, David N Louis9, Daniel P Cahill8, Matthew Meyerson16.
Abstract
IMPORTANCE: Conclusive intraoperative pathologic confirmation of diffuse infiltrative glioma guides the decision to pursue definitive neurosurgical resection. Establishing the intraoperative diagnosis by histologic analysis can be difficult in low-cellularity infiltrative gliomas. Therefore, we developed a rapid and sensitive genotyping assay to detect somatic single-nucleotide variants in the telomerase reverse transcriptase (TERT) promoter and isocitrate dehydrogenase 1 (IDH1). OBSERVATIONS: This assay was applied to tissue samples from 190 patients with diffuse gliomas, including archived fixed and frozen specimens and tissue obtained intraoperatively. Results demonstrated 96% sensitivity (95% CI, 90%-99%) and 100% specificity (95% CI, 95%-100%) for World Health Organization grades II and III gliomas. In a series of live cases, glioma-defining mutations could be identified within 60 minutes, which could facilitate the diagnosis in an intraoperative timeframe. CONCLUSIONS AND RELEVANCE: The genotyping method described herein can establish the diagnosis of low-cellularity tumors like glioma and could be adapted to the point-of-care diagnosis of other lesions that are similarly defined by highly recurrent somatic mutations.Entities:
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Year: 2015 PMID: 26181761 PMCID: PMC4872045 DOI: 10.1001/jamaoncol.2015.0917
Source DB: PubMed Journal: JAMA Oncol ISSN: 2374-2437 Impact factor: 31.777