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Therapeutic implications of improved molecular diagnostics for rare CNS embryonal tumor entities: results of an international, retrospective study.

Authors :
von Hoff K
Haberler C
Schmitt-Hoffner F
Schepke E
de Rojas T
Jacobs S
Zapotocky M
Sumerauer D
Perek-Polnik M
Dufour C
van Vuurden D
Slavc I
Gojo J
Pickles JC
Gerber NU
Massimino M
Gil-da-Costa MJ
Garami M
Kumirova E
Sehested A
Scheie D
Cruz O
Moreno L
Cho J
Zeller B
Bovenschen N
Grotzer M
Alderete D
Snuderl M
Zheludkova O
Golanov A
Okonechnikov K
Mynarek M
Juhnke BO
Rutkowski S
Schüller U
Pizer B
von Zezschwitz B
Kwiecien R
Wechsung M
Konietschke F
Hwang EI
Sturm D
Pfister SM
von Deimling A
Rushing EJ
Ryzhova M
Hauser P
Łastowska M
Wesseling P
Giangaspero F
Hawkins C
Figarella-Branger D
Eberhart C
Burger P
Gessi M
Korshunov A
Jacques TS
Capper D
Pietsch T
Kool M
Source :
Neuro-oncology [Neuro Oncol] 2021 Sep 01; Vol. 23 (9), pp. 1597-1611.
Publication Year :
2021

Abstract

Background: Only few data are available on treatment-associated behavior of distinct rare CNS embryonal tumor entities previously treated as "CNS-primitive neuroectodermal tumors" (CNS-PNET). Respective data on specific entities, including CNS neuroblastoma, FOXR2 activated (CNS NB-FOXR2), and embryonal tumors with multilayered rosettes (ETMR) are needed for development of differentiated treatment strategies.<br />Methods: Within this retrospective, international study, tumor samples of clinically well-annotated patients with the original diagnosis of CNS-PNET were analyzed using DNA methylation arrays (n = 307). Additional cases (n = 66) with DNA methylation pattern of CNS NB-FOXR2 were included irrespective of initial histological diagnosis. Pooled clinical data (n = 292) were descriptively analyzed.<br />Results: DNA methylation profiling of "CNS-PNET" classified 58 (19%) cases as ETMR, 57 (19%) as high-grade glioma (HGG), 36 (12%) as CNS NB-FOXR2, and 89(29%) cases were classified into 18 other entities. Sixty-seven (22%) cases did not show DNA methylation patterns similar to established CNS tumor reference classes. Best treatment results were achieved for CNS NB-FOXR2 patients (5-year PFS: 63% ± 7%, OS: 85% ± 5%, n = 63), with 35/42 progression-free survivors after upfront craniospinal irradiation (CSI) and chemotherapy. The worst outcome was seen for ETMR and HGG patients with 5-year PFS of 18% ± 6% and 22% ± 7%, and 5-year OS of 24% ± 6% and 25% ± 7%, respectively.<br />Conclusion: The historically reported poor outcome of CNS-PNET patients becomes highly variable when tumors are molecularly classified based on DNA methylation profiling. Patients with CNS NB-FOXR2 responded well to current treatments and a standard-risk CSI-based regimen may be prospectively evaluated. The poor outcome of ETMR across applied treatment strategies substantiates the necessity for evaluation of novel treatments.<br /> (© The Author(s) 2021. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.)

Details

Language :
English
ISSN :
1523-5866
Volume :
23
Issue :
9
Database :
MEDLINE
Journal :
Neuro-oncology
Publication Type :
Academic Journal
Accession number :
34077956
Full Text :
https://doi.org/10.1093/neuonc/noab136