Please use this identifier to cite or link to this item: https://hdl.handle.net/1/2353
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dc.contributor.authorKnight, A-
dc.contributor.authorHorsley, P-
dc.contributor.authorYuile, A-
dc.contributor.authorYim, J-
dc.contributor.authorSuh, M-
dc.contributor.authorVenketesha, V-
dc.contributor.authorKastelan, M-
dc.contributor.authorWheeler, H-
dc.contributor.authorBack, Michael-
dc.date.accessioned2023-05-16T23:53:34Z-
dc.date.available2023-05-16T23:53:34Z-
dc.date.issued2023-05-
dc.identifier.citation163(1):281-288en
dc.identifier.urihttps://hdl.handle.net/1/2353-
dc.description.abstractH3K27M- and H3G34R-mutant gliomas are recently-classified subgroups of high-grade gliomas (HGGs) affecting younger adults. This study aimed to describe patterns of infiltration and failure, and the volumetric response of these tumours to radiotherapy. Patients with histone-mutant gliomas aged 16-50 years, managed from 2009 to 2021 were identified and clinical, radiological and histopathological characteristics collected. Tumour volume was assessed on MRI at diagnosis, pre-radiotherapy, month + 1, + 3 and + 5 post-radiation and at relapse. Of 538 IDH1/2 wild-type HGGs, 18(15%) had a histone alteration. Eleven were H3K27M- and 7 H3G34R-mutant respectively. Median age at diagnosis was 20 years (range17-48 years). Median overall survival was 20 months (95%CI 14-29 months). Both H3K27M- and H3G34R-mutant tumours exhibited extensive T2F infiltration involving a median of 4 neuroanatomical subsites at diagnosis. Median volume of disease pre-radiotherapy on T1gd and T2F respectively was 0.5cm3 (IQR:0-1.7cm3) and 11.9 cm3 (IQR:7.5-29.6cm3) for H3K27M and 0.9cm3 (IQR:0-8.4cm3) and 43.8cm3 (IQR:25.2-86.6 cm3) for H3G34R tumours. T2F volume reduction > 50% was observed 3-months post-IMRT in 7(64%) patients with H3K27M and 1(14%) with H3G34R tumours. Fourteen patients had relapsed. Relapse was local-only, distant-only and both in 4(44%), 3(33%) and 2(22%) H3K27M-mutant and 1(20%), 2(40%), and 2(40%) H3G34R-mutant tumours. On last scan before death, leptomeningeal spread was present in 4/8(50%) and 1/5(20%) and subependymal spread in 4/8 (50%) and 0/5 H3K27M- and G34R-mutant cases respectively. H3K27M-mutant gliomas are highly responsive to radiotherapy but exhibit high propensity for subsequent leptomeningeal and subependymal spread. H3G34R-mutant tumours exhibit lesser early volumetric response to radiotherapy and propensity for distant in-brain failure.en
dc.description.sponsorshipRadiation Oncologyen
dc.subjectRadiologyen
dc.subjectRadiotherapyen
dc.subjectCanceren
dc.titleVolumetric response and pattern of failure of histone altered high grade glioma in adults following management with radiation therapyen
dc.typeJournal Articleen
dc.identifier.doi10.1007/s11060-023-04332-4en
dc.description.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/37184742en
dc.description.affiliatesCentral Coast Local Health Districten
dc.description.affiliatesGosford Hospitalen
dc.identifier.journaltitleJournal of Neuro-Oncologyen
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeJournal Article-
item.fulltextNo Fulltext-
item.grantfulltextnone-
crisitem.author.deptRadiation Oncology-
Appears in Collections:Oncology / Cancer
Radiology
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