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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 | 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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