Please use this identifier to cite or link to this item: https://dora.health.qld.gov.au/qldresearchjspui/handle/1/3699
Title: Molecular grouping and outcomes of young children with newly diagnosed ependymoma treated on the multi-institutional SJYC07 trial
Authors: Indelicato, D. J.
Boop, F. A.
Merchant, T. E.
Ellison, D. W.
Gajjar, A.
Bendel, A. E.
Hassall, T.
Crawford, J. R.
Partap, S.
Fisher, P. G.
Tatevossian, R. G.
Seah, T.
Qaddoumi, I. A.
Vinitsky, A.
Armstrong, G. T.
Sabin, N. D.
Tinkle, C. L.
Klimo, P.
Upadhyaya, S. A.
Robinson, G. W.
Onar-Thomas, A.
Orr, B. A.
Billups, C. A.
Bowers, D. C.
Issue Date: 2019
Source: 21, (10), 2019, p. 1319-1330
Pages: 1319-1330
Journal: Neuro-Oncology
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
2021-04-27
DOI: 10.1093/neuonc/noz069
Resources: https://www.embase.com/search/results?subaction=viewrecord&id=L629904486&from=exporthttp://dx.doi.org/10.1093/neuonc/noz069 |
Keywords: fluorescence in situ hybridization;follow up;hearing impairment;histopathology;human;low drug dose;maintenance therapy;major clinical study;male;metastasis;molecular diagnosis;multicenter study;multiple cycle treatment;overall survival;pediatric patient;phase 2 clinical trial;preschool child;prospective study;radiation necrosis;side effect;tumor localization;progression free survival;genetic analyzerInfinium Methylation EPIC BeadChip;carboplatin;cisplatin;cyclophosphamide;erlotinib;etoposide;folinic acid;genomic DNA;methotrexate;topotecan;tumor marker;unclassified drug;v-rel avian reticuloendotheliosis viral oncogene homolog A;vincristine;YAP signaling protein;article;bone marrow suppression;cancer chemotherapy;cancer grading;cancer surgery;cancer survival;cerebrospinal fluid;child;chromosome 1q;classifier;clinical feature;clinical outcome;clinical target volume;cohort analysis;conformal radiotherapy;consolidation chemotherapy;DNA methylation;drug megadose;ependymoma;febrile neutropenia;female
Type: Article
Appears in Sites:Children's Health Queensland Publications

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