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Evaluation of the rapid Idylla IDH1-2 mutation assay in FFPE glioma samples.
Solomon, James P; Munoz-Zuluaga, Carlos; Slocum, Cheyanne; Dillard, Alicia; Cong, Lin; Wang, Jiajing; Lindeman, Neal; Kluk, Michael; Liechty, Benjamin; Pisapia, David; Rennert, Hanna; Velu, Priya D.
Afiliação
  • Solomon JP; Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, 1300 York Avenue Suite C-302, New York, NY, 10065, USA.
  • Munoz-Zuluaga C; NewYork-Presbyterian Hospital, 525 East 68th Street Suite F-540, New York, NY, 10065, USA.
  • Slocum C; NewYork-Presbyterian Hospital, 525 East 68th Street Suite F-540, New York, NY, 10065, USA.
  • Dillard A; NewYork-Presbyterian Hospital, 525 East 68th Street Suite F-540, New York, NY, 10065, USA.
  • Cong L; NewYork-Presbyterian Hospital, 525 East 68th Street Suite F-540, New York, NY, 10065, USA.
  • Wang J; NewYork-Presbyterian Hospital, 525 East 68th Street Suite F-540, New York, NY, 10065, USA.
  • Lindeman N; Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, 1300 York Avenue Suite C-302, New York, NY, 10065, USA.
  • Kluk M; Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, 1300 York Avenue Suite C-302, New York, NY, 10065, USA.
  • Liechty B; NewYork-Presbyterian Hospital, 525 East 68th Street Suite F-540, New York, NY, 10065, USA.
  • Pisapia D; Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, 1300 York Avenue Suite C-302, New York, NY, 10065, USA.
  • Rennert H; NewYork-Presbyterian Hospital, 525 East 68th Street Suite F-540, New York, NY, 10065, USA.
  • Velu PD; Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, 1300 York Avenue Suite C-302, New York, NY, 10065, USA.
Diagn Pathol ; 19(1): 70, 2024 May 25.
Article em En | MEDLINE | ID: mdl-38796421
ABSTRACT
IDH1 and IDH2 mutational status is a critical biomarker with diagnostic, prognostic, and treatment implications in glioma. Although IDH1 p.R132H-specific immunohistochemistry is available, it is unable to identify other mutations in IDH1/2. Next-generation sequencing can accurately determine IDH1/2 mutational status but suffers from long turnaround time when urgent treatment planning and initiation is medically necessary. The Idylla assay can detect IDH1/2 mutational status from unstained formalin-fixed paraffin-embedded (FFPE) slides in as little as a few hours. In a clinical validation, we demonstrate clinical accuracy of 97% compared to next-generation sequencing. Sensitivity studies demonstrated a limit of detection of 2.5-5% variant allele frequency, even at DNA inputs below the manufacturer's recommended threshold. Overall, the assay is an effective and accurate method for rapid determination of IDH1/2 mutational status.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Encefálicas / Glioma / Isocitrato Desidrogenase / Mutação Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Encefálicas / Glioma / Isocitrato Desidrogenase / Mutação Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article