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Medulloblastoma in adults: evaluation of the Dutch society for neuro-oncology treatment protocol

PURPOSE: Medulloblastoma is a rare tumor in adults. The objective of this nationwide, multicenter study was to evaluate the toxicity and efficacy of the Dutch treatment protocol for adult medulloblastoma patients. METHODS: Adult medulloblastoma patients diagnosed between 2010 and 2018 were identifie...

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Autores principales: Bleeker, L., Kouwenhoven, M. C. M., de Heer, I., Lissenberg-Witte, B. I., Gijsbers, A. H., Dubbink, H. J., Kros, J. M., Gijtenbeek, J. M. M., Kurt, E., van der Rijt, C. C. D., Swaak-Kragten, A. T., de Vos, F. Y., van der Weide, H. L., French, P. J., van den Bent, M. J., Wesseling, P., Bromberg, J. E. C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10050065/
https://www.ncbi.nlm.nih.gov/pubmed/36920679
http://dx.doi.org/10.1007/s11060-023-04285-8
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author Bleeker, L.
Kouwenhoven, M. C. M.
de Heer, I.
Lissenberg-Witte, B. I.
Gijsbers, A. H.
Dubbink, H. J.
Kros, J. M.
Gijtenbeek, J. M. M.
Kurt, E.
van der Rijt, C. C. D.
Swaak-Kragten, A. T.
de Vos, F. Y.
van der Weide, H. L.
French, P. J.
van den Bent, M. J.
Wesseling, P.
Bromberg, J. E. C.
author_facet Bleeker, L.
Kouwenhoven, M. C. M.
de Heer, I.
Lissenberg-Witte, B. I.
Gijsbers, A. H.
Dubbink, H. J.
Kros, J. M.
Gijtenbeek, J. M. M.
Kurt, E.
van der Rijt, C. C. D.
Swaak-Kragten, A. T.
de Vos, F. Y.
van der Weide, H. L.
French, P. J.
van den Bent, M. J.
Wesseling, P.
Bromberg, J. E. C.
author_sort Bleeker, L.
collection PubMed
description PURPOSE: Medulloblastoma is a rare tumor in adults. The objective of this nationwide, multicenter study was to evaluate the toxicity and efficacy of the Dutch treatment protocol for adult medulloblastoma patients. METHODS: Adult medulloblastoma patients diagnosed between 2010 and 2018 were identified in the Dutch rare tumors registry or nationwide pathology database. Patients with intention to treat according to the national treatment protocol were included. Risk stratification was performed based on residual disease, histological subtype and extent of disease. All patients received postoperative radiotherapy [craniospinal axis 36 Gy/fossa posterior boost 19.8 Gy (14.4 Gy in case of metastases)]. High-risk patients received additional neoadjuvant (carboplatin-etoposide), concomitant (vincristine) and adjuvant chemotherapy (carboplatin-vincristine-cyclophosphamide) as far as feasible by toxicity. Methylation profiling, and additional next-generation sequencing in case of SHH-activated medulloblastomas, were performed. RESULTS: Forty-seven medulloblastoma patients were identified, of whom 32 were treated according to the protocol. Clinical information and tumor material was available for 28 and 20 patients, respectively. The histological variants were mainly classic (43%) and desmoplastic medulloblastoma (36%). Sixteen patients (57%) were considered standard-risk and 60% were SHH-activated medulloblastomas. Considerable treatment reductions and delays in treatment occurred due to especially hematological and neurotoxicity. Only one high-risk patient could complete all chemotherapy courses. 5-years progression-free survival (PFS) and overall survival (OS) for standard-risk patients appeared worse than for high-risk patients (PFS 69% vs. 90%, OS 81% vs. 90% respectively), although this wasn’t statistically significant. CONCLUSION: Combined chemo-radiotherapy is a toxic regimen for adult medulloblastoma patients that may result in improved survival.
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spelling pubmed-100500652023-03-30 Medulloblastoma in adults: evaluation of the Dutch society for neuro-oncology treatment protocol Bleeker, L. Kouwenhoven, M. C. M. de Heer, I. Lissenberg-Witte, B. I. Gijsbers, A. H. Dubbink, H. J. Kros, J. M. Gijtenbeek, J. M. M. Kurt, E. van der Rijt, C. C. D. Swaak-Kragten, A. T. de Vos, F. Y. van der Weide, H. L. French, P. J. van den Bent, M. J. Wesseling, P. Bromberg, J. E. C. J Neurooncol Case Study PURPOSE: Medulloblastoma is a rare tumor in adults. The objective of this nationwide, multicenter study was to evaluate the toxicity and efficacy of the Dutch treatment protocol for adult medulloblastoma patients. METHODS: Adult medulloblastoma patients diagnosed between 2010 and 2018 were identified in the Dutch rare tumors registry or nationwide pathology database. Patients with intention to treat according to the national treatment protocol were included. Risk stratification was performed based on residual disease, histological subtype and extent of disease. All patients received postoperative radiotherapy [craniospinal axis 36 Gy/fossa posterior boost 19.8 Gy (14.4 Gy in case of metastases)]. High-risk patients received additional neoadjuvant (carboplatin-etoposide), concomitant (vincristine) and adjuvant chemotherapy (carboplatin-vincristine-cyclophosphamide) as far as feasible by toxicity. Methylation profiling, and additional next-generation sequencing in case of SHH-activated medulloblastomas, were performed. RESULTS: Forty-seven medulloblastoma patients were identified, of whom 32 were treated according to the protocol. Clinical information and tumor material was available for 28 and 20 patients, respectively. The histological variants were mainly classic (43%) and desmoplastic medulloblastoma (36%). Sixteen patients (57%) were considered standard-risk and 60% were SHH-activated medulloblastomas. Considerable treatment reductions and delays in treatment occurred due to especially hematological and neurotoxicity. Only one high-risk patient could complete all chemotherapy courses. 5-years progression-free survival (PFS) and overall survival (OS) for standard-risk patients appeared worse than for high-risk patients (PFS 69% vs. 90%, OS 81% vs. 90% respectively), although this wasn’t statistically significant. CONCLUSION: Combined chemo-radiotherapy is a toxic regimen for adult medulloblastoma patients that may result in improved survival. Springer US 2023-03-15 2023 /pmc/articles/PMC10050065/ /pubmed/36920679 http://dx.doi.org/10.1007/s11060-023-04285-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Case Study
Bleeker, L.
Kouwenhoven, M. C. M.
de Heer, I.
Lissenberg-Witte, B. I.
Gijsbers, A. H.
Dubbink, H. J.
Kros, J. M.
Gijtenbeek, J. M. M.
Kurt, E.
van der Rijt, C. C. D.
Swaak-Kragten, A. T.
de Vos, F. Y.
van der Weide, H. L.
French, P. J.
van den Bent, M. J.
Wesseling, P.
Bromberg, J. E. C.
Medulloblastoma in adults: evaluation of the Dutch society for neuro-oncology treatment protocol
title Medulloblastoma in adults: evaluation of the Dutch society for neuro-oncology treatment protocol
title_full Medulloblastoma in adults: evaluation of the Dutch society for neuro-oncology treatment protocol
title_fullStr Medulloblastoma in adults: evaluation of the Dutch society for neuro-oncology treatment protocol
title_full_unstemmed Medulloblastoma in adults: evaluation of the Dutch society for neuro-oncology treatment protocol
title_short Medulloblastoma in adults: evaluation of the Dutch society for neuro-oncology treatment protocol
title_sort medulloblastoma in adults: evaluation of the dutch society for neuro-oncology treatment protocol
topic Case Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10050065/
https://www.ncbi.nlm.nih.gov/pubmed/36920679
http://dx.doi.org/10.1007/s11060-023-04285-8
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