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DNA methylation-array interlaboratory comparison trial demonstrates highly reproducible paediatric CNS tumour classification across 13 international centres.

Authors :
Chirica M
Jurmeister P
Teichmann D
Koch A
Perez E
Schmid S
Simon M
Driever PH
Bodden C
van Tilburg CM
Hardin EC
Lavarino C
Hench J
Scheie D
Cryan J
Vicha A
Buttarelli FR
Michiels A
Haberler C
Barahona P
Tops BBJ
Jacques T
Stokland T
Witt O
Jones DTW
Capper D
Source :
Neuropathology and applied neurobiology [Neuropathol Appl Neurobiol] 2024 Oct; Vol. 50 (5), pp. e13010.
Publication Year :
2024

Abstract

Aims: DNA methylation profiling, recently endorsed by the World Health Organisation (WHO) as a pivotal diagnostic tool for brain tumours, most commonly relies on bead arrays. Despite its widespread use, limited data exist on the technical reproducibility and potential cross-institutional differences. The LOGGIC Core BioClinical Data Bank registry conducted a prospective laboratory comparison trial with 12 international laboratories to enhance diagnostic accuracy for paediatric low-grade gliomas, focusing on technical aspects of DNA methylation data generation and profile interpretation under clinical real-time conditions.<br />Methods: Four representative low-grade gliomas of distinct histologies were centrally selected, and DNA extraction was performed. Participating laboratories received a DNA aliquot and performed the DNA methylation-based classification and result interpretation without knowledge of tumour histology. Additionally, participants were required to interpret the copy number profile derived from DNA methylation data and conduct DNA sequencing of the BRAF hotspot p.V600 due to its relevance for low-grade gliomas. Results had to be returned within 30 days.<br />Results: High technical reproducibility was observed, with a median pairwise correlation of 0.99 (range 0.94-0.99) between coordinating laboratory and participants. DNA methylation-based tumour classification and copy number profile interpretation were consistent across all centres, and BRAF mutation status was accurately reported for all cases. Eleven out of 12 centres successfully reported their analysis within the 30-day timeframe.<br />Conclusion: Our study demonstrates remarkable concordance in DNA methylation profiling and profile interpretation across 12 international centres. These findings underscore the potential contribution of DNA methylation analysis to the harmonisation of brain tumour diagnostics.<br /> (© 2024 The Author(s). Neuropathology and Applied Neurobiology published by John Wiley & Sons Ltd on behalf of British Neuropathological Society.)

Details

Language :
English
ISSN :
1365-2990
Volume :
50
Issue :
5
Database :
MEDLINE
Journal :
Neuropathology and applied neurobiology
Publication Type :
Academic Journal
Accession number :
39410806
Full Text :
https://doi.org/10.1111/nan.13010