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https://dora.health.qld.gov.au/qldresearchjspui/handle/1/7152
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DC Field | Value | Language |
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dc.contributor.author | Pillay-Smiley, N. | - |
dc.contributor.author | Webster, A. | - |
dc.contributor.author | Lane, A. | - |
dc.contributor.author | Hawkins, C. | - |
dc.contributor.author | Hassall, T. | - |
dc.contributor.author | Leach, J. | - |
dc.contributor.author | Jones, B. | - |
dc.contributor.author | Dorris, K. | - |
dc.contributor.author | Hansford, J. R. | - |
dc.contributor.author | Zaghloul, M. | - |
dc.contributor.author | Cheng, S. | - |
dc.contributor.author | Hummel, T. R. | - |
dc.contributor.author | Hoffman, L. M. | - |
dc.contributor.author | Warren, K. E. | - |
dc.date.accessioned | 2025-05-27T03:50:35Z | - |
dc.date.available | 2025-05-27T03:50:35Z | - |
dc.date.issued | 2024 | - |
dc.identifier.citation | Neuro-Oncology, 2024 (26) p.iv34 | en |
dc.identifier.uri | https://dora.health.qld.gov.au/qldresearchjspui/handle/1/7152 | - |
dc.description.abstract | BACKGROUND: Given that radiation therapy is the only treatment modality demonstrated to result in any clinical benefit for children with DIPG, re-irradiation therapy has been explored as a treatment option for progressive DIPG. Several studies suggest re-irradiation is feasible, and may lengthen survival for children with progressive DIPG. However, any re-irradiation benefits are unclear and no standard of care (dose, fractionation, volume, timing, clinical status) has been defined. The aims of this study are to evaluate re-radiation therapy practices for children with progressive DIPG/DMG and to define a historical cohort of children with DIPG/ DMG who have received re-radiation (re-XRT) for progressive DIPG/DMG. METHODS: Data was extracted from the International DIPG Registry, and analyzed with descriptive statistics. RESULTS: Of 1214 patients in the iDIPG Registry, 113 receiving re-XRT. Patients were diagnosed between 2002-2022, with the majority of patients diagnosed over the last decade. Of those 113 patients with specified data, at re-irradiation, n=68 (60%) received photon and n= 4 (4%) were treated with proton radiation. The median dose at re-XRT was 25 Gy (20-30 IQR) in 10 fractions (10-14 IQR). Time between initial XRT and re-XRT was 41.5 weeks (29.5-54 weeks). OS from diagnosis was 18 months (range, 15-23 mo); OS from re-XRT was 6 months (range, 4-10 mo). CONCLUSIONS: Re-radiation therapy for children with DIPG/DMG is becoming a more common practice and appears to have OS benefit, with post-progression OS of 6 mo comparing favorably to historical data of 2.3 mo. [Cooney T et al, Neuro Oncol 2017] Efforts are underway to define patient selection and tolerability. Data extraction from the SIOPE DIPG/DMG Registry is also ongoing; data from both registries will be collated and uniformly presented. | - |
dc.language.iso | English | - |
dc.title | RE-IRRADIATION PRACTICES AND OUTCOMES IN PATIENTS WITH DIPG/DMG: A REPORT FROM THE INTERNATIONAL DIPG REGISTRY | - |
dc.type | Conference Abstract | - |
dc.identifier.doi | 10.1093/neuonc/noae064.120 | - |
dc.relation.url | https://www.embase.com/search/results?subaction=viewrecord&id=L645031540&from=export | - |
dc.relation.url | http://dx.doi.org/10.1093/neuonc/noae064.120 | - |
dc.identifier.journaltitle | Neuro-Oncology | - |
dc.identifier.risid | 643 | - |
dc.description.pages | iv34 | - |
dc.description.volume | 26 | - |
item.grantfulltext | none | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.cerifentitytype | Publications | - |
item.languageiso639-1 | English | - |
item.openairetype | Conference Abstract | - |
item.fulltext | No Fulltext | - |
Appears in Sites: | Children's Health Queensland Publications Queensland Health Publications |
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