Cargando…

HGG-29. How I treat recurrent pediatric high-grade glioma (HGG): A Europe-wide survey study.

PURPOSE: Prognosis of pediatric high-grade gliomas (pedHGG) is dismal, and there is no standard of care treatment in case of recurrence/progression. We aimed to gain an overview of different treatment strategies in the setting of recurrent/progressing pedHGG. METHODS: In a web-based questionnaire, m...

Descripción completa

Detalles Bibliográficos
Autores principales: Perwein, Thomas, Giese, Barbara, Nussbaumer, Gunther, von Bueren, André O, van Buiren, Miriam, Benesch, Martin, Kramm, Christof Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9164810/
http://dx.doi.org/10.1093/neuonc/noac079.244
_version_ 1784720227461758976
author Perwein, Thomas
Giese, Barbara
Nussbaumer, Gunther
von Bueren, André O
van Buiren, Miriam
Benesch, Martin
Kramm, Christof Maria
author_facet Perwein, Thomas
Giese, Barbara
Nussbaumer, Gunther
von Bueren, André O
van Buiren, Miriam
Benesch, Martin
Kramm, Christof Maria
author_sort Perwein, Thomas
collection PubMed
description PURPOSE: Prognosis of pediatric high-grade gliomas (pedHGG) is dismal, and there is no standard of care treatment in case of recurrence/progression. We aimed to gain an overview of different treatment strategies in the setting of recurrent/progressing pedHGG. METHODS: In a web-based questionnaire, members of the SIOPE-BTG and the GPOH were surveyed on different therapeutic options in four real-world case scenarios (children/adolescents with recurrent/progressing HGG). RESULTS: One hundred and thirty-nine clinicians with experience in pediatric neuro-oncology from 22 European countries participated in the survey. Most respondents preferred further active (multimodal) oncological treatment in three out of four cases and chose palliative care with pure symptom control measures only in one case (gliomatosis cerebri and marked symptoms). Depending on the case, 8-92% of experts would initiate a re-resection (maximal safe resection in case of localized hemispheric pedHGG), combined with molecular diagnostics, and 55-77% recommended (re-)irradiation, preferably local radiotherapy >20 Gy (or craniospinal irradiation in one case with disseminated spinal HGG, 65%). Throughout all case scenarios, most respondents would participate in clinical trials and use targeted therapy (79-99%), depending on molecular genetic findings (BRAF alterations: BRAF/MEK inhibitors, 64-88%; EGFR overexpression: anti-EGFR treatment, 46%; SMARCB1 deletion: EZH2 inhibitor, 12%). 31-72% would administer chemotherapy (CCNU, 17%; PCV, 8%; temozolomide, 19%; oral etoposide/trofosfamide, 8%), and 20-69% advocated immunotherapy (checkpoint inhibitors, 30%; tumor vaccines, 16%). Depending on the individual case, respondents would also include bevacizumab (6-18%), HDAC inhibitors (4-15%), tumor-treating fields (1-26%), and intraventricular chemotherapy (4-24%). CONCLUSIONS: In each case, experts would combine conventional multimodal treatment concepts, including re-irradiation, with targeted therapy based on molecular genetic findings. International cooperative trials combining a standard (chemo-)therapy backbone with targeted therapy approaches for defined subgroups may help to gain valid clinical data and improve treatment in pediatric patients with recurrent/progressive HGG.
format Online
Article
Text
id pubmed-9164810
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-91648102022-06-05 HGG-29. How I treat recurrent pediatric high-grade glioma (HGG): A Europe-wide survey study. Perwein, Thomas Giese, Barbara Nussbaumer, Gunther von Bueren, André O van Buiren, Miriam Benesch, Martin Kramm, Christof Maria Neuro Oncol High Grade Glioma PURPOSE: Prognosis of pediatric high-grade gliomas (pedHGG) is dismal, and there is no standard of care treatment in case of recurrence/progression. We aimed to gain an overview of different treatment strategies in the setting of recurrent/progressing pedHGG. METHODS: In a web-based questionnaire, members of the SIOPE-BTG and the GPOH were surveyed on different therapeutic options in four real-world case scenarios (children/adolescents with recurrent/progressing HGG). RESULTS: One hundred and thirty-nine clinicians with experience in pediatric neuro-oncology from 22 European countries participated in the survey. Most respondents preferred further active (multimodal) oncological treatment in three out of four cases and chose palliative care with pure symptom control measures only in one case (gliomatosis cerebri and marked symptoms). Depending on the case, 8-92% of experts would initiate a re-resection (maximal safe resection in case of localized hemispheric pedHGG), combined with molecular diagnostics, and 55-77% recommended (re-)irradiation, preferably local radiotherapy >20 Gy (or craniospinal irradiation in one case with disseminated spinal HGG, 65%). Throughout all case scenarios, most respondents would participate in clinical trials and use targeted therapy (79-99%), depending on molecular genetic findings (BRAF alterations: BRAF/MEK inhibitors, 64-88%; EGFR overexpression: anti-EGFR treatment, 46%; SMARCB1 deletion: EZH2 inhibitor, 12%). 31-72% would administer chemotherapy (CCNU, 17%; PCV, 8%; temozolomide, 19%; oral etoposide/trofosfamide, 8%), and 20-69% advocated immunotherapy (checkpoint inhibitors, 30%; tumor vaccines, 16%). Depending on the individual case, respondents would also include bevacizumab (6-18%), HDAC inhibitors (4-15%), tumor-treating fields (1-26%), and intraventricular chemotherapy (4-24%). CONCLUSIONS: In each case, experts would combine conventional multimodal treatment concepts, including re-irradiation, with targeted therapy based on molecular genetic findings. International cooperative trials combining a standard (chemo-)therapy backbone with targeted therapy approaches for defined subgroups may help to gain valid clinical data and improve treatment in pediatric patients with recurrent/progressive HGG. Oxford University Press 2022-06-03 /pmc/articles/PMC9164810/ http://dx.doi.org/10.1093/neuonc/noac079.244 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle High Grade Glioma
Perwein, Thomas
Giese, Barbara
Nussbaumer, Gunther
von Bueren, André O
van Buiren, Miriam
Benesch, Martin
Kramm, Christof Maria
HGG-29. How I treat recurrent pediatric high-grade glioma (HGG): A Europe-wide survey study.
title HGG-29. How I treat recurrent pediatric high-grade glioma (HGG): A Europe-wide survey study.
title_full HGG-29. How I treat recurrent pediatric high-grade glioma (HGG): A Europe-wide survey study.
title_fullStr HGG-29. How I treat recurrent pediatric high-grade glioma (HGG): A Europe-wide survey study.
title_full_unstemmed HGG-29. How I treat recurrent pediatric high-grade glioma (HGG): A Europe-wide survey study.
title_short HGG-29. How I treat recurrent pediatric high-grade glioma (HGG): A Europe-wide survey study.
title_sort hgg-29. how i treat recurrent pediatric high-grade glioma (hgg): a europe-wide survey study.
topic High Grade Glioma
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9164810/
http://dx.doi.org/10.1093/neuonc/noac079.244
work_keys_str_mv AT perweinthomas hgg29howitreatrecurrentpediatrichighgradegliomahggaeuropewidesurveystudy
AT giesebarbara hgg29howitreatrecurrentpediatrichighgradegliomahggaeuropewidesurveystudy
AT nussbaumergunther hgg29howitreatrecurrentpediatrichighgradegliomahggaeuropewidesurveystudy
AT vonbuerenandreo hgg29howitreatrecurrentpediatrichighgradegliomahggaeuropewidesurveystudy
AT vanbuirenmiriam hgg29howitreatrecurrentpediatrichighgradegliomahggaeuropewidesurveystudy
AT beneschmartin hgg29howitreatrecurrentpediatrichighgradegliomahggaeuropewidesurveystudy
AT krammchristofmaria hgg29howitreatrecurrentpediatrichighgradegliomahggaeuropewidesurveystudy