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Prognostic impact of distinct genetic entities in pediatric diffuse glioma WHO-grade II : Report from the German/Swiss SIOP-LGG 2004 cohort

Authors :
Torsten Pietsch
Ulrich-Wilhelm Thomale
Rene Schmidt
Daniela Kandels
Fabian Falkenstein
Eberhard Maaß
Beate Timmermann
Rolf-Dieter Kortmann
Ho Keung Ng
Michael H. Albert
Arnulf Pekrun
Juergen Krauss
Astrid Gnekow
Monika Warmuth-Metz
Marco Gessi
Brigitte Bison
Publication Year :
2020

Abstract

Reports on pediatric low-grade diffuse glioma WHO-grade II (DG2) suggest an impaired survival rate, but lack conclusive results for genetically defined DG2-entities. We analyzed the natural history, treatment and prognosis of DG2 and investigated which genetically defined sub-entities proved unfavorable for survival. Within the prospectively registered, population-based German/Swiss SIOP-LGG 2004 cohort 100 patients (age 0.8-17.8 years, 4% neurofibromatosis [NF1]) were diagnosed with a DG2. Following biopsy (41%) or variable extent of resection (59%), 65 patients received no adjuvant treatment. Radiologic progression or severe neurologic symptoms prompted chemotherapy (n = 18) or radiotherapy (n = 17). Multiple lines of salvage treatment were necessary for 19/35 patients. Five years event-free survival dropped to 0.44, while 5 years overall survival was 0.90 (median observation time 8.3 years). Extensive genetic profiling of 65/100 DG2 identified Histone3-K27M-mutation in 4, IDH1-mutation in 11, BRAF-V600-mutation in 12, KIAA1549-BRAF-fusions in 6 patients, while the remaining 32 tumor tissues did not show alterations of these genes. Progression to malignant glioma occurred in 12 cases of all genetically defined subgroups within a range of 0.5 to 10.8 years, except for tumors carrying KIAA1549-BRAF-fusions. Histone3-K27M-mutant tumors proved uniformly fatal within 0.6 to 2.4 years. The current LGG treatment strategy seems appropriate for all DG2-entities, with the exemption of Histone3-K27M-mutant tumors that require a HGG-related treatment strategy. Our data confirm the importance to genetically define pediatric low-grade diffuse gliomas for proper treatment decisions and risk assessment.

Details

Language :
English
Database :
OpenAIRE
Accession number :
edsair.doi.dedup.....e8e87e74d1d9feae1a23491131dfb044