Please use this identifier to cite or link to this item:
https://dora.health.qld.gov.au/qldresearchjspui/handle/1/3699
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Indelicato, D. J. | en |
dc.contributor.author | Boop, F. A. | en |
dc.contributor.author | Merchant, T. E. | en |
dc.contributor.author | Ellison, D. W. | en |
dc.contributor.author | Gajjar, A. | en |
dc.contributor.author | Bendel, A. E. | en |
dc.contributor.author | Hassall, T. | en |
dc.contributor.author | Crawford, J. R. | en |
dc.contributor.author | Partap, S. | en |
dc.contributor.author | Fisher, P. G. | en |
dc.contributor.author | Tatevossian, R. G. | en |
dc.contributor.author | Seah, T. | en |
dc.contributor.author | Qaddoumi, I. A. | en |
dc.contributor.author | Vinitsky, A. | en |
dc.contributor.author | Armstrong, G. T. | en |
dc.contributor.author | Sabin, N. D. | en |
dc.contributor.author | Tinkle, C. L. | en |
dc.contributor.author | Klimo, P. | en |
dc.contributor.author | Upadhyaya, S. A. | en |
dc.contributor.author | Robinson, G. W. | en |
dc.contributor.author | Onar-Thomas, A. | en |
dc.contributor.author | Orr, B. A. | en |
dc.contributor.author | Billups, C. A. | en |
dc.contributor.author | Bowers, D. C. | en |
dc.date.accessioned | 2022-11-07T23:45:11Z | - |
dc.date.available | 2022-11-07T23:45:11Z | - |
dc.date.issued | 2019 | en |
dc.identifier.citation | 21, (10), 2019, p. 1319-1330 | en |
dc.identifier.other | RIS | en |
dc.identifier.uri | http://dora.health.qld.gov.au/qldresearchjspui/handle/1/3699 | - |
dc.description.abstract | Background. This report documents the clinical characteristics, molecular grouping, and outcome of young children with ependymoma treated prospectively on a clinical trial. Methods. Fifty-four children (aged ≤3 y) with newly diagnosed ependymoma were treated on the St Jude Young Children 07 (SJYC07) trial with maximal safe surgical resection, 4 cycles of systemic chemotherapy, consolidation therapy using focal conformal radiation therapy (RT) (5-mm clinical target volume), and 6 months of oral maintenance chemotherapy. Molecular groups were determined by tumor DNA methylation using Infinium Methylation EPIC BeadChip and profiled on the German Cancer Research Center/Molecular Neuropathology 2.0 classifier. Results. One of the 54 study patients had metastases (cerebrospinal fluid positive) at diagnosis. Gross or neartotal resection was achieved in 48 (89%) patients prior to RT. At a median follow-up of 4.4 years (range, 0.2-10.3 y), 4-year progression-free survival (PFS) was 75.1% ±7.2%, and overall survival was 92.6% ±4.4%. The molecular groups showed no significant difference in PFS (4-year estimates: Posterior fossa ependymoma group A [PF-EPN-A; 42/54], 71.2% ±8.3%; supratentorial ependymoma positive for v-rel avian reticuloendotheliosis viral oncogene homolog A [ST-EPN-RELA; 8/54], 83.3% ±17.0%; and supratentorial ependymoma positive for Yes-associated protein [4/54], 100%, P = 0.22). Subtotal resection prior to RT was associated with an inferior PFS compared with gross or near-total resection (4-year PFS: 41.7% ±22.5% vs 79.0% ±7.1%, P = 0.024), as was PF-EPN-A group with 1q gain (P = 0.05). Histopathologic grading was not associated with outcomes (classic vs anaplastic; P = 0.89). Conclusions. In this prospectively treated cohort of young children with ependymoma, ST-EPN-RELA tumors had a more favorable outcome than reported from retrospective data. Histologic grade did not impact outcome. PF-EPN-A with 1q gain and subtotal resection were associated with inferior outcomes.L6299044862019-11-26 <br />2021-04-27 <br /> | en |
dc.language.iso | en | en |
dc.relation.ispartof | Neuro-Oncology | en |
dc.title | Molecular grouping and outcomes of young children with newly diagnosed ependymoma treated on the multi-institutional SJYC07 trial | en |
dc.type | Article | en |
dc.identifier.doi | 10.1093/neuonc/noz069 | en |
dc.subject.keywords | fluorescence in situ hybridization | en |
dc.subject.keywords | follow up | en |
dc.subject.keywords | hearing impairment | en |
dc.subject.keywords | histopathology | en |
dc.subject.keywords | human | en |
dc.subject.keywords | low drug dose | en |
dc.subject.keywords | maintenance therapy | en |
dc.subject.keywords | major clinical study | en |
dc.subject.keywords | male | en |
dc.subject.keywords | metastasis | en |
dc.subject.keywords | molecular diagnosis | en |
dc.subject.keywords | multicenter study | en |
dc.subject.keywords | multiple cycle treatment | en |
dc.subject.keywords | overall survival | en |
dc.subject.keywords | pediatric patient | en |
dc.subject.keywords | phase 2 clinical trial | en |
dc.subject.keywords | preschool child | en |
dc.subject.keywords | prospective study | en |
dc.subject.keywords | radiation necrosis | en |
dc.subject.keywords | side effect | en |
dc.subject.keywords | tumor localization | en |
dc.subject.keywords | progression free survival | en |
dc.subject.keywords | genetic analyzerInfinium Methylation EPIC BeadChip | en |
dc.subject.keywords | carboplatin | en |
dc.subject.keywords | cisplatin | en |
dc.subject.keywords | cyclophosphamide | en |
dc.subject.keywords | erlotinib | en |
dc.subject.keywords | etoposide | en |
dc.subject.keywords | folinic acid | en |
dc.subject.keywords | genomic DNA | en |
dc.subject.keywords | methotrexate | en |
dc.subject.keywords | topotecan | en |
dc.subject.keywords | tumor marker | en |
dc.subject.keywords | unclassified drug | en |
dc.subject.keywords | v-rel avian reticuloendotheliosis viral oncogene homolog A | en |
dc.subject.keywords | vincristine | en |
dc.subject.keywords | YAP signaling protein | en |
dc.subject.keywords | article | en |
dc.subject.keywords | bone marrow suppression | en |
dc.subject.keywords | cancer chemotherapy | en |
dc.subject.keywords | cancer grading | en |
dc.subject.keywords | cancer surgery | en |
dc.subject.keywords | cancer survival | en |
dc.subject.keywords | cerebrospinal fluid | en |
dc.subject.keywords | child | en |
dc.subject.keywords | chromosome 1q | en |
dc.subject.keywords | classifier | en |
dc.subject.keywords | clinical feature | en |
dc.subject.keywords | clinical outcome | en |
dc.subject.keywords | clinical target volume | en |
dc.subject.keywords | cohort analysis | en |
dc.subject.keywords | conformal radiotherapy | en |
dc.subject.keywords | consolidation chemotherapy | en |
dc.subject.keywords | DNA methylation | en |
dc.subject.keywords | drug megadose | en |
dc.subject.keywords | ependymoma | en |
dc.subject.keywords | febrile neutropenia | en |
dc.subject.keywords | female | en |
dc.relation.url | https://www.embase.com/search/results?subaction=viewrecord&id=L629904486&from=exporthttp://dx.doi.org/10.1093/neuonc/noz069 | | en |
dc.identifier.risid | 2871 | en |
dc.description.pages | 1319-1330 | en |
item.grantfulltext | none | - |
item.openairetype | Article | - |
item.fulltext | No Fulltext | - |
item.languageiso639-1 | en | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.cerifentitytype | Publications | - |
Appears in Sites: | Children's Health Queensland Publications |
Items in DORA are protected by copyright, with all rights reserved, unless otherwise indicated.