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Prospective genomically guided identification of “early/evolving” and “undersampled” IDH-wildtype glioblastoma leads to improved clinical outcomes

BACKGROUND: Genomic profiling studies of diffuse gliomas have led to new improved classification schemes that better predict patient outcomes compared to conventional histomorphology alone. One example is the recognition that patients with IDH-wildtype diffuse astrocytic gliomas demonstrating lower-...

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Autores principales: Zhang, Yalan, Lucas, Calixto-Hope G, Young, Jacob S, Morshed, Ramin A, McCoy, Lucie, Oberheim Bush, Nancy Ann, Taylor, Jennie W, Daras, Mariza, Butowski, Nicholas A, Villanueva-Meyer, Javier E, Cha, Soonmee, Wrensch, Margaret, Wiencke, John K, Lee, Julieann C, Pekmezci, Melike, Phillips, Joanna J, Perry, Arie, Bollen, Andrew W, Aghi, Manish K, Theodosopoulos, Philip, Chang, Edward F, Hervey-Jumper, Shawn L, Berger, Mitchel S, Clarke, Jennifer L, Chang, Susan M, Molinaro, Annette M, Solomon, David A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9527525/
https://www.ncbi.nlm.nih.gov/pubmed/35395677
http://dx.doi.org/10.1093/neuonc/noac089
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author Zhang, Yalan
Lucas, Calixto-Hope G
Young, Jacob S
Morshed, Ramin A
McCoy, Lucie
Oberheim Bush, Nancy Ann
Taylor, Jennie W
Daras, Mariza
Butowski, Nicholas A
Villanueva-Meyer, Javier E
Cha, Soonmee
Wrensch, Margaret
Wiencke, John K
Lee, Julieann C
Pekmezci, Melike
Phillips, Joanna J
Perry, Arie
Bollen, Andrew W
Aghi, Manish K
Theodosopoulos, Philip
Chang, Edward F
Hervey-Jumper, Shawn L
Berger, Mitchel S
Clarke, Jennifer L
Chang, Susan M
Molinaro, Annette M
Solomon, David A
author_facet Zhang, Yalan
Lucas, Calixto-Hope G
Young, Jacob S
Morshed, Ramin A
McCoy, Lucie
Oberheim Bush, Nancy Ann
Taylor, Jennie W
Daras, Mariza
Butowski, Nicholas A
Villanueva-Meyer, Javier E
Cha, Soonmee
Wrensch, Margaret
Wiencke, John K
Lee, Julieann C
Pekmezci, Melike
Phillips, Joanna J
Perry, Arie
Bollen, Andrew W
Aghi, Manish K
Theodosopoulos, Philip
Chang, Edward F
Hervey-Jumper, Shawn L
Berger, Mitchel S
Clarke, Jennifer L
Chang, Susan M
Molinaro, Annette M
Solomon, David A
author_sort Zhang, Yalan
collection PubMed
description BACKGROUND: Genomic profiling studies of diffuse gliomas have led to new improved classification schemes that better predict patient outcomes compared to conventional histomorphology alone. One example is the recognition that patients with IDH-wildtype diffuse astrocytic gliomas demonstrating lower-grade histologic features but genomic and/or epigenomic profile characteristic of glioblastoma typically have poor outcomes similar to patients with histologically diagnosed glioblastoma. Here we sought to determine the clinical impact of prospective genomic profiling for these IDH-wildtype diffuse astrocytic gliomas lacking high-grade histologic features but with molecular profile of glioblastoma. METHODS: Clinical management and outcomes were analyzed for 38 consecutive adult patients with IDH-wildtype diffuse astrocytic gliomas lacking necrosis or microvascular proliferation on histologic examination that were genomically profiled on a prospective clinical basis revealing criteria for an integrated diagnosis of “diffuse astrocytic glioma, IDH-wildtype, with molecular features of glioblastoma, WHO grade IV” per cIMPACT-NOW criteria. RESULTS: We identified that this diagnosis consists of two divergent clinical scenarios based on integration of radiologic, histologic, and genomic features that we term “early/evolving” and “undersampled” glioblastoma, IDH-wildtype. We found that prospective genomically guided identification of early/evolving and undersampled IDH-wildtype glioblastoma resulted in more aggressive patient management and improved clinical outcomes compared to a biologically matched historical control patient cohort receiving standard-of-care therapy based on histomorphologic diagnosis alone. CONCLUSIONS: These results support routine use of genomic and/or epigenomic profiling to accurately classify glial neoplasms, as these assays not only improve diagnostic classification but critically lead to more appropriate patient management that can improve clinical outcomes.
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spelling pubmed-95275252022-10-03 Prospective genomically guided identification of “early/evolving” and “undersampled” IDH-wildtype glioblastoma leads to improved clinical outcomes Zhang, Yalan Lucas, Calixto-Hope G Young, Jacob S Morshed, Ramin A McCoy, Lucie Oberheim Bush, Nancy Ann Taylor, Jennie W Daras, Mariza Butowski, Nicholas A Villanueva-Meyer, Javier E Cha, Soonmee Wrensch, Margaret Wiencke, John K Lee, Julieann C Pekmezci, Melike Phillips, Joanna J Perry, Arie Bollen, Andrew W Aghi, Manish K Theodosopoulos, Philip Chang, Edward F Hervey-Jumper, Shawn L Berger, Mitchel S Clarke, Jennifer L Chang, Susan M Molinaro, Annette M Solomon, David A Neuro Oncol Clinical Investigations BACKGROUND: Genomic profiling studies of diffuse gliomas have led to new improved classification schemes that better predict patient outcomes compared to conventional histomorphology alone. One example is the recognition that patients with IDH-wildtype diffuse astrocytic gliomas demonstrating lower-grade histologic features but genomic and/or epigenomic profile characteristic of glioblastoma typically have poor outcomes similar to patients with histologically diagnosed glioblastoma. Here we sought to determine the clinical impact of prospective genomic profiling for these IDH-wildtype diffuse astrocytic gliomas lacking high-grade histologic features but with molecular profile of glioblastoma. METHODS: Clinical management and outcomes were analyzed for 38 consecutive adult patients with IDH-wildtype diffuse astrocytic gliomas lacking necrosis or microvascular proliferation on histologic examination that were genomically profiled on a prospective clinical basis revealing criteria for an integrated diagnosis of “diffuse astrocytic glioma, IDH-wildtype, with molecular features of glioblastoma, WHO grade IV” per cIMPACT-NOW criteria. RESULTS: We identified that this diagnosis consists of two divergent clinical scenarios based on integration of radiologic, histologic, and genomic features that we term “early/evolving” and “undersampled” glioblastoma, IDH-wildtype. We found that prospective genomically guided identification of early/evolving and undersampled IDH-wildtype glioblastoma resulted in more aggressive patient management and improved clinical outcomes compared to a biologically matched historical control patient cohort receiving standard-of-care therapy based on histomorphologic diagnosis alone. CONCLUSIONS: These results support routine use of genomic and/or epigenomic profiling to accurately classify glial neoplasms, as these assays not only improve diagnostic classification but critically lead to more appropriate patient management that can improve clinical outcomes. Oxford University Press 2022-04-08 /pmc/articles/PMC9527525/ /pubmed/35395677 http://dx.doi.org/10.1093/neuonc/noac089 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Clinical Investigations
Zhang, Yalan
Lucas, Calixto-Hope G
Young, Jacob S
Morshed, Ramin A
McCoy, Lucie
Oberheim Bush, Nancy Ann
Taylor, Jennie W
Daras, Mariza
Butowski, Nicholas A
Villanueva-Meyer, Javier E
Cha, Soonmee
Wrensch, Margaret
Wiencke, John K
Lee, Julieann C
Pekmezci, Melike
Phillips, Joanna J
Perry, Arie
Bollen, Andrew W
Aghi, Manish K
Theodosopoulos, Philip
Chang, Edward F
Hervey-Jumper, Shawn L
Berger, Mitchel S
Clarke, Jennifer L
Chang, Susan M
Molinaro, Annette M
Solomon, David A
Prospective genomically guided identification of “early/evolving” and “undersampled” IDH-wildtype glioblastoma leads to improved clinical outcomes
title Prospective genomically guided identification of “early/evolving” and “undersampled” IDH-wildtype glioblastoma leads to improved clinical outcomes
title_full Prospective genomically guided identification of “early/evolving” and “undersampled” IDH-wildtype glioblastoma leads to improved clinical outcomes
title_fullStr Prospective genomically guided identification of “early/evolving” and “undersampled” IDH-wildtype glioblastoma leads to improved clinical outcomes
title_full_unstemmed Prospective genomically guided identification of “early/evolving” and “undersampled” IDH-wildtype glioblastoma leads to improved clinical outcomes
title_short Prospective genomically guided identification of “early/evolving” and “undersampled” IDH-wildtype glioblastoma leads to improved clinical outcomes
title_sort prospective genomically guided identification of “early/evolving” and “undersampled” idh-wildtype glioblastoma leads to improved clinical outcomes
topic Clinical Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9527525/
https://www.ncbi.nlm.nih.gov/pubmed/35395677
http://dx.doi.org/10.1093/neuonc/noac089
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