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Published in: Child's Nervous System 2/2016

01-02-2016 | Original Paper

Embryonal tumors with multilayered rosettes in children: the SFCE experience

Authors: Meryl Horwitz, Christelle Dufour, Pierre Leblond, Franck Bourdeaut, Cécile Faure-Conter, Anne-Isabelle Bertozzi, Marie Bernadette Delisle, Gilles Palenzuela, Anne Jouvet, Didier Scavarda, Matthieu Vinchon, Laetitia Padovani, Jean Gaudart, Dominique Figarella Branger, Nicolas Andre

Published in: Child's Nervous System | Issue 2/2016

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Abstract

Purposes

The purpose of this study was to retrospectively study embryonal tumors with multilayered rosettes (ETMR), a rare new entity that gathers ETAN-TR (embryonal tumor with abundant neuropil and true rosettes), ependymoblastomas, and medulloepitheliomas, in order to improve their descriptions and try to better define therapeutic modalities.

Methods

Patients with ETMR, ETAN-TR, ependymoblastoma, and medulloepithelioma treated in SFCE centres (Société Française de lutte contre les Cancers et les leucémies de l'Enfant et de l'adolescent) since 2000 were collected. Data were retrieved from clinical charts.

Results

Thirty-eight patients were included in the analysis. Seventeen had an ETAN-TR, 13 had a medulloepithelioma, and 8 had an ETMR. No ependymoblastoma was included. The median age at diagnosis was 31 months (range, 2.8–141 months). The predominant tumor location was supratentorial (66 %); 18.4 % patients had metastatic lesion.
LIN28A expression was positive in 11/11 patients. Amplification of the locus 19q13.42 was positive in 10/12 patients. Thirty patients were treated according to the primitive neuroectodermal tumors of high risk (PNET-HR) protocol. The median time of follow-up was 0.9 years (range 0.1 to 15.3 years). The 1-year event-free survival (EFS) and overall survival (OS) were, respectively, 36 % CI 95 % (23–55) and 45 % CI 95 % (31–64). On multivariate analysis, complete surgical resection, radiotherapy, and high-dose chemotherapy were associated with a better overall survival with a relative risk of, respectively, 7.9 CI 95 % (2.6–23.5) p < 0.0002, 41.8 CI 95 % (9.4–186) p < 0.0001, and 3.5 CI 95 % (1.3–9.5) p = 0.012.

Conclusion

Prognosis of ETMR remains dismal despite multimodal therapy. LIN28A immunostaining and 19q13.42 amplification should be systematically done to secure the diagnosis. Complete surgical resection, radiotherapy, and high-dose chemotherapy are associated with better outcome.
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Metadata
Title
Embryonal tumors with multilayered rosettes in children: the SFCE experience
Authors
Meryl Horwitz
Christelle Dufour
Pierre Leblond
Franck Bourdeaut
Cécile Faure-Conter
Anne-Isabelle Bertozzi
Marie Bernadette Delisle
Gilles Palenzuela
Anne Jouvet
Didier Scavarda
Matthieu Vinchon
Laetitia Padovani
Jean Gaudart
Dominique Figarella Branger
Nicolas Andre
Publication date
01-02-2016
Publisher
Springer Berlin Heidelberg
Published in
Child's Nervous System / Issue 2/2016
Print ISSN: 0256-7040
Electronic ISSN: 1433-0350
DOI
https://doi.org/10.1007/s00381-015-2920-2

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