Literature DB >> 32483596

Is Next-Generation Sequencing Alone Sufficient to Reliably Diagnose Gliomas?

Kwok Ling Kam1, Christina L Appin2, Qinwen Mao1, Sachie Ikegami3, Rimas V Lukas4, Marina N Nikiforova5, Somak Roy5, Daniel J Brat1, Craig Horbinski1.   

Abstract

The power and widespread use of next-generation sequencing (NGS) in surgical neuropathology has raised questions as to whether NGS might someday fully supplant histologic-based examination. We therefore sought to determine the feasibility of relying on NGS alone for diagnosing infiltrating gliomas. A total of 171 brain lesions in adults, all of which had been analyzed by GlioSeq NGS, comprised the study cohort. Each case was separately diagnosed by 6 reviewers, based solely on age, sex, tumor location, and NGS results. Results were compared with the final integrated diagnoses and scored on the following scale: 0 = either wrong tumor type or correct tumor type but off by 2+ grades; 1 = off by 1 grade; 2 = exactly correct. Histology alone was treated as a seventh reviewer. Overall reviewer accuracy ranged from 81.6% to 94.2%, while histology alone scored 87.1%. For glioblastomas, NGS was more accurate than histology alone (93.8%-97.9% vs 87.5%). The NGS accuracy for grade II and III astrocytoma and oligodendroglioma was only 54.3%-84.8% and 34.4%-87.5%, respectively. Most uncommon gliomas, including BRAF-driven tumors, could not be accurately classified just by NGS. These data indicate that, even in this era of advanced molecular diagnostics, histologic evaluation is still an essential part of optimal patient care.
© 2020 American Association of Neuropathologists, Inc. All rights reserved.

Entities:  

Keywords:  Astrocytoma; Glioblastoma; Glioma; Histology; Next-generation sequencing; Oligodendroglioma

Mesh:

Year:  2020        PMID: 32483596      PMCID: PMC7304984          DOI: 10.1093/jnen/nlaa044

Source DB:  PubMed          Journal:  J Neuropathol Exp Neurol        ISSN: 0022-3069            Impact factor:   3.685


  19 in total

1.  PI3K/AKT pathway mutations cause a spectrum of brain malformations from megalencephaly to focal cortical dysplasia.

Authors:  Laura A Jansen; Ghayda M Mirzaa; Gisele E Ishak; Brian J O'Roak; Joseph B Hiatt; William H Roden; Sonya A Gunter; Susan L Christian; Sarah Collins; Carissa Adams; Jean-Baptiste Rivière; Judith St-Onge; Jeffrey G Ojemann; Jay Shendure; Robert F Hevner; William B Dobyns
Journal:  Brain       Date:  2015-02-25       Impact factor: 13.501

2.  A decade's perspective on DNA sequencing technology.

Authors:  Elaine R Mardis
Journal:  Nature       Date:  2011-02-10       Impact factor: 49.962

3.  cIMPACT-NOW update 2: diagnostic clarifications for diffuse midline glioma, H3 K27M-mutant and diffuse astrocytoma/anaplastic astrocytoma, IDH-mutant.

Authors:  David N Louis; Caterina Giannini; David Capper; Werner Paulus; Dominique Figarella-Branger; M Beatriz Lopes; Tracy T Batchelor; J Gregory Cairncross; Martin van den Bent; Wolfgang Wick; Pieter Wesseling
Journal:  Acta Neuropathol       Date:  2018-03-01       Impact factor: 17.088

4.  cIMPACT-NOW update 1: Not Otherwise Specified (NOS) and Not Elsewhere Classified (NEC).

Authors:  David N Louis; Pieter Wesseling; Werner Paulus; Caterina Giannini; Tracy T Batchelor; J Gregory Cairncross; David Capper; Dominique Figarella-Branger; M Beatriz Lopes; Wolfgang Wick; Martin van den Bent
Journal:  Acta Neuropathol       Date:  2018-01-25       Impact factor: 17.088

5.  Targeted next-generation sequencing panel (GlioSeq) provides comprehensive genetic profiling of central nervous system tumors.

Authors:  Marina N Nikiforova; Abigail I Wald; Melissa A Melan; Somak Roy; Shan Zhong; Ronald L Hamilton; Frank S Lieberman; Jan Drappatz; Nduka M Amankulor; Ian F Pollack; Yuri E Nikiforov; Craig Horbinski
Journal:  Neuro Oncol       Date:  2015-12-17       Impact factor: 12.300

Review 6.  The medical necessity of advanced molecular testing in the diagnosis and treatment of brain tumor patients.

Authors:  Craig Horbinski; Keith L Ligon; Priscilla Brastianos; Jason T Huse; Monica Venere; Susan Chang; Jan Buckner; Timothy Cloughesy; Robert B Jenkins; Caterina Giannini; Roger Stupp; L Burt Nabors; Patrick Y Wen; Kenneth J Aldape; Rimas V Lukas; Evanthia Galanis; Charles G Eberhart; Daniel J Brat; Jann N Sarkaria
Journal:  Neuro Oncol       Date:  2019-12-17       Impact factor: 12.300

7.  cIMPACT-NOW update 3: recommended diagnostic criteria for "Diffuse astrocytic glioma, IDH-wildtype, with molecular features of glioblastoma, WHO grade IV".

Authors:  Daniel J Brat; Kenneth Aldape; Howard Colman; Eric C Holland; David N Louis; Robert B Jenkins; B K Kleinschmidt-DeMasters; Arie Perry; Guido Reifenberger; Roger Stupp; Andreas von Deimling; Michael Weller
Journal:  Acta Neuropathol       Date:  2018-09-26       Impact factor: 17.088

8.  Multi-faceted computational assessment of risk and progression in oligodendroglioma implicates NOTCH and PI3K pathways.

Authors:  Lee A D Cooper; Daniel J Brat; Sameer H Halani; Safoora Yousefi; Jose Velazquez Vega; Michael R Rossi; Zheng Zhao; Fatemeh Amrollahi; Chad A Holder; Amelia Baxter-Stoltzfus; Jennifer Eschbacher; Brent Griffith; Jeffrey J Olson; Tao Jiang; Joseph R Yates; Charles G Eberhart; Laila M Poisson
Journal:  NPJ Precis Oncol       Date:  2018-11-06

Review 9.  Pleomorphic xanthoastrocytoma: a brief review.

Authors:  Nawal Shaikh; Nupur Brahmbhatt; Tim J Kruser; Kwok L Kam; Christina L Appin; Nitin Wadhwani; James Chandler; Priya Kumthekar; Rimas V Lukas
Journal:  CNS Oncol       Date:  2019-09-19

10.  CDKN2A homozygous deletion is a strong adverse prognosis factor in diffuse malignant IDH-mutant gliomas.

Authors:  Romain Appay; Caroline Dehais; Claude-Alain Maurage; Agusti Alentorn; Catherine Carpentier; Carole Colin; François Ducray; Fabienne Escande; Ahmed Idbaih; Aurélie Kamoun; Yannick Marie; Karima Mokhtari; Emeline Tabouret; Nesrine Trabelsi; Emmanuelle Uro-Coste; Jean-Yves Delattre; Dominique Figarella-Branger
Journal:  Neuro Oncol       Date:  2019-12-17       Impact factor: 13.029

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