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SPDR-2 Histopathological investigation of the oligodendroglial tumors resected following alkylating agent chemotherapy

Oligodendrogliomas, i.e., lower grade gliomas with 1p/19q codeletion, are often responsive to chemotherapy, however, those tumors eventually recur and life-limiting in the majority of patients despite initial chemotherapeutic response. We have been treating those patients with upfront chemotherapy a...

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Autores principales: Masato, Nakaya, Kanazawa, Tokunori, Ohara, Kentaro, Kitamura, Yohei, Yoshida, Kazunari, Sasaki, Hikaru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8648213/
http://dx.doi.org/10.1093/noajnl/vdab159.011
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author Masato, Nakaya
Kanazawa, Tokunori
Ohara, Kentaro
Kitamura, Yohei
Yoshida, Kazunari
Sasaki, Hikaru
author_facet Masato, Nakaya
Kanazawa, Tokunori
Ohara, Kentaro
Kitamura, Yohei
Yoshida, Kazunari
Sasaki, Hikaru
author_sort Masato, Nakaya
collection PubMed
description Oligodendrogliomas, i.e., lower grade gliomas with 1p/19q codeletion, are often responsive to chemotherapy, however, those tumors eventually recur and life-limiting in the majority of patients despite initial chemotherapeutic response. We have been treating those patients with upfront chemotherapy and subsequent resection following tumor volume decrease since 2006. This study aimed to elucidate the histological changes and the mechanism of recurrence after alkylating agent chemotherapy in oligodendrogliomas. Fifteen oligodendrogliomas (Grade 2: 12, Grade 3: 3) resected following tumor volume decrease after alkylating agent chemotherapy were included and compared with their pre-chemotherapy specimens. Histological changes were investigated using hematoxylin-eosin staining, and changes in proliferative activity, status of glioma stem cells (GSCs), and tumor-infiltrating macrophages were assessed using immunohistochemistry. The frequent histological findings following chemotherapy included a sparse glial background, abundant foamy cell infiltration, gliosis, calcification, and nuclear degradation. The Ki-67/MIB-1 index decreased and the number of macrophages increased after chemotherapy. Moreover, the ratio of GSCs to total tumor cells increased after chemotherapy. GSCs and macrophages constitute the mechanism of resistance to and recurrence after alkylating agent chemotherapy in oligodendrogliomas.
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spelling pubmed-86482132021-12-07 SPDR-2 Histopathological investigation of the oligodendroglial tumors resected following alkylating agent chemotherapy Masato, Nakaya Kanazawa, Tokunori Ohara, Kentaro Kitamura, Yohei Yoshida, Kazunari Sasaki, Hikaru Neurooncol Adv Supplement Abstracts Oligodendrogliomas, i.e., lower grade gliomas with 1p/19q codeletion, are often responsive to chemotherapy, however, those tumors eventually recur and life-limiting in the majority of patients despite initial chemotherapeutic response. We have been treating those patients with upfront chemotherapy and subsequent resection following tumor volume decrease since 2006. This study aimed to elucidate the histological changes and the mechanism of recurrence after alkylating agent chemotherapy in oligodendrogliomas. Fifteen oligodendrogliomas (Grade 2: 12, Grade 3: 3) resected following tumor volume decrease after alkylating agent chemotherapy were included and compared with their pre-chemotherapy specimens. Histological changes were investigated using hematoxylin-eosin staining, and changes in proliferative activity, status of glioma stem cells (GSCs), and tumor-infiltrating macrophages were assessed using immunohistochemistry. The frequent histological findings following chemotherapy included a sparse glial background, abundant foamy cell infiltration, gliosis, calcification, and nuclear degradation. The Ki-67/MIB-1 index decreased and the number of macrophages increased after chemotherapy. Moreover, the ratio of GSCs to total tumor cells increased after chemotherapy. GSCs and macrophages constitute the mechanism of resistance to and recurrence after alkylating agent chemotherapy in oligodendrogliomas. Oxford University Press 2021-12-06 /pmc/articles/PMC8648213/ http://dx.doi.org/10.1093/noajnl/vdab159.011 Text en © The Author(s) 2021. Published by Oxford University Press, the Society for Neuro-Oncology and the European Association of 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.
spellingShingle Supplement Abstracts
Masato, Nakaya
Kanazawa, Tokunori
Ohara, Kentaro
Kitamura, Yohei
Yoshida, Kazunari
Sasaki, Hikaru
SPDR-2 Histopathological investigation of the oligodendroglial tumors resected following alkylating agent chemotherapy
title SPDR-2 Histopathological investigation of the oligodendroglial tumors resected following alkylating agent chemotherapy
title_full SPDR-2 Histopathological investigation of the oligodendroglial tumors resected following alkylating agent chemotherapy
title_fullStr SPDR-2 Histopathological investigation of the oligodendroglial tumors resected following alkylating agent chemotherapy
title_full_unstemmed SPDR-2 Histopathological investigation of the oligodendroglial tumors resected following alkylating agent chemotherapy
title_short SPDR-2 Histopathological investigation of the oligodendroglial tumors resected following alkylating agent chemotherapy
title_sort spdr-2 histopathological investigation of the oligodendroglial tumors resected following alkylating agent chemotherapy
topic Supplement Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8648213/
http://dx.doi.org/10.1093/noajnl/vdab159.011
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