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DOI 10.1093/neuonc/noad055

Медицинская библиотека · Neuro-oncology · 2023

Optimizing biomarkers for accurate ependymoma diagnosis, prognostication, and stratification within International Clinical Trials: A BIOMECA study.

Chapman Rebecca J, Ghasemi David R, Andreiuolo Felipe, Zschernack Valentina, Espariat Arnault Tauziede, Buttarelli Francesca R, Giangaspero Felice, Grill Jacques, Haberler Christine, Paine Simon M L, Scott Ian, Jacques Thomas S, Sill Martin, Pfister Stefan, Kilday John-Paul, Leblond Pierre, Massimino Maura, Witt Hendrik, Modena Piergiorgio, Varlet Pascale, Pietsch Torsten, Grundy Richard G, Pajtler Kristian W, Ritzmann Timothy A

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUND

Accurate identification of brain tumor molecular subgroups is increasingly important. We aimed to establish the most accurate and reproducible ependymoma subgroup biomarker detection techniques, across 147 cases from International Society of Pediatric Oncology (SIOP) Ependymoma II trial participants, enrolled in the pan-European "Biomarkers of Ependymoma in Children and Adolescents (BIOMECA)" study.

METHODS

Across 6 European BIOMECA laboratories, we evaluated epigenetic profiling (DNA methylation array); immunohistochemistry (IHC) for nuclear p65-RELA, H3K27me3, and Tenascin-C; copy number analysis via fluorescent in situ hybridization (FISH) and MLPA (1q, CDKN2A), and MIP and DNA methylation array (genome-wide copy number evaluation); analysis of ZFTA- and YAP1-fusions by RT-PCR and sequencing, Nanostring and break-apart FISH.

RESULTS

DNA Methylation profiling classified 65.3% (n = 96/147) of cases as EPN-PFA and 15% (n = 22/147) as ST-ZFTA fusion-positive. Immunohistochemical loss of H3K27me3 was a reproducible and accurate surrogate marker for EPN-PFA (sensitivity 99%-100% across 3 centers). IHC for p65-RELA, FISH, and RNA-based analyses effectively identified ZFTA- and YAP-fused supratentorial ependymomas. Detection of 1q gain using FISH exhibited only 57% inter-center concordance and low sensitivity and specificity while MIP, MLPA, and DNA methylation-based approaches demonstrated greater accuracy.

CONCLUSIONS

We confirm, in a prospective trial cohort, that H3K27me3 immunohistochemistry is a robust EPN-PFA biomarker. Tenascin-C should be abandoned as a PFA marker. DNA methylation and MIP arrays are effective tools for copy number analysis of 1q gain, 6q, and CDKN2A loss while FISH is inadequate. Fusion detection was successful, but rare novel fusions need more extensive technologies. Finally, we propose test sets to guide future diagnostic approaches.

Для цитирования: Chapman Rebecca J, Ghasemi David R, Andreiuolo Felipe, Zschernack Valentina, Espariat Arnault Tauziede, Buttarelli Francesca R, Giangaspero Felice, Grill Jacques, Haberler Christine, Paine Simon M L, Scott Ian, Jacques Thomas S, Sill Martin, Pfister Stefan, Kilday John-Paul, Leblond Pierre, Massimino Maura, Witt Hendrik, Modena Piergiorgio, Varlet Pascale, Pietsch Torsten, Grundy Richard G, Pajtler Kristian W, Ritzmann Timothy A. Optimizing biomarkers for accurate ependymoma diagnosis, prognostication, and stratification within International Clinical Trials: A BIOMECA study.. Neuro-oncology. 2023. DOI: 10.1093/neuonc/noad055.

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