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Characteristics of Anaplastic Oligodendrogliomas Short-Term Survivors: A POLA Network Study
BACKGROUND: Anaplastic oligodendrogliomas IDH-mutant and 1p/19q codeleted (AO) occasionally have a poor outcome. Herein we aimed at analyzing their characteristics. METHODS: We retrospectively analyzed the characteristics of 44 AO patients with a cancer-specific survival <5 years (short-term surv...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9074983/ https://www.ncbi.nlm.nih.gov/pubmed/35522558 http://dx.doi.org/10.1093/oncolo/oyac023 |
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author | Garnier, Louis Vidal, Chrystelle Chinot, Olivier Cohen-Jonathan Moyal, Elisabeth Djelad, Apolline Bronnimann, Charlotte Bekaert, Lien Taillandier, Luc Frenel, Jean-Sébastien Langlois, Olivier Colin, Philippe Menei, Philippe Dhermain, Frédéric Carpentier, Catherine Gerazime, Aurélie Curtit, Elsa Figarella-Branger, Dominique Dehais, Caroline Ducray, François |
author_facet | Garnier, Louis Vidal, Chrystelle Chinot, Olivier Cohen-Jonathan Moyal, Elisabeth Djelad, Apolline Bronnimann, Charlotte Bekaert, Lien Taillandier, Luc Frenel, Jean-Sébastien Langlois, Olivier Colin, Philippe Menei, Philippe Dhermain, Frédéric Carpentier, Catherine Gerazime, Aurélie Curtit, Elsa Figarella-Branger, Dominique Dehais, Caroline Ducray, François |
author_sort | Garnier, Louis |
collection | PubMed |
description | BACKGROUND: Anaplastic oligodendrogliomas IDH-mutant and 1p/19q codeleted (AO) occasionally have a poor outcome. Herein we aimed at analyzing their characteristics. METHODS: We retrospectively analyzed the characteristics of 44 AO patients with a cancer-specific survival <5 years (short-term survivors, STS) and compared them with those of 146 AO patients with a survival ≥5 years (classical survivors, CS) included in the POLA network. RESULTS: Compared to CS, STS were older (P = .0001), less frequently presented with isolated seizures (P < .0001), more frequently presented with cognitive dysfunction (P < .0001), had larger tumors (P = .= .003), a higher proliferative index (P = .= .0003), and a higher number of chromosomal arm abnormalities (P = .= .02). Regarding treatment, STS less frequently underwent a surgical resection than CS (P = .= .0001) and were more frequently treated with chemotherapy alone (P = .= .009) or with radiotherapy plus temozolomide (P = .= .05). Characteristics independently associated with STS in multivariate analysis were cognitive dysfunction, a number of mitosis > 8, and the absence of tumor resection. Based on cognitive dysfunction, type of surgery, and number of mitosis, patients could be classified into groups of standard (18%) and high (62%) risk of <5 year survival. CONCLUSION: The present study suggests that although STS poor outcome appears to largely result from a more advanced disease at diagnosis, surgical resection may be particularly important in this population. |
format | Online Article Text |
id | pubmed-9074983 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-90749832022-05-09 Characteristics of Anaplastic Oligodendrogliomas Short-Term Survivors: A POLA Network Study Garnier, Louis Vidal, Chrystelle Chinot, Olivier Cohen-Jonathan Moyal, Elisabeth Djelad, Apolline Bronnimann, Charlotte Bekaert, Lien Taillandier, Luc Frenel, Jean-Sébastien Langlois, Olivier Colin, Philippe Menei, Philippe Dhermain, Frédéric Carpentier, Catherine Gerazime, Aurélie Curtit, Elsa Figarella-Branger, Dominique Dehais, Caroline Ducray, François Oncologist Neuro-Oncology BACKGROUND: Anaplastic oligodendrogliomas IDH-mutant and 1p/19q codeleted (AO) occasionally have a poor outcome. Herein we aimed at analyzing their characteristics. METHODS: We retrospectively analyzed the characteristics of 44 AO patients with a cancer-specific survival <5 years (short-term survivors, STS) and compared them with those of 146 AO patients with a survival ≥5 years (classical survivors, CS) included in the POLA network. RESULTS: Compared to CS, STS were older (P = .0001), less frequently presented with isolated seizures (P < .0001), more frequently presented with cognitive dysfunction (P < .0001), had larger tumors (P = .= .003), a higher proliferative index (P = .= .0003), and a higher number of chromosomal arm abnormalities (P = .= .02). Regarding treatment, STS less frequently underwent a surgical resection than CS (P = .= .0001) and were more frequently treated with chemotherapy alone (P = .= .009) or with radiotherapy plus temozolomide (P = .= .05). Characteristics independently associated with STS in multivariate analysis were cognitive dysfunction, a number of mitosis > 8, and the absence of tumor resection. Based on cognitive dysfunction, type of surgery, and number of mitosis, patients could be classified into groups of standard (18%) and high (62%) risk of <5 year survival. CONCLUSION: The present study suggests that although STS poor outcome appears to largely result from a more advanced disease at diagnosis, surgical resection may be particularly important in this population. Oxford University Press 2022-03-05 /pmc/articles/PMC9074983/ /pubmed/35522558 http://dx.doi.org/10.1093/oncolo/oyac023 Text en © The Author(s) 2022. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Neuro-Oncology Garnier, Louis Vidal, Chrystelle Chinot, Olivier Cohen-Jonathan Moyal, Elisabeth Djelad, Apolline Bronnimann, Charlotte Bekaert, Lien Taillandier, Luc Frenel, Jean-Sébastien Langlois, Olivier Colin, Philippe Menei, Philippe Dhermain, Frédéric Carpentier, Catherine Gerazime, Aurélie Curtit, Elsa Figarella-Branger, Dominique Dehais, Caroline Ducray, François Characteristics of Anaplastic Oligodendrogliomas Short-Term Survivors: A POLA Network Study |
title | Characteristics of Anaplastic Oligodendrogliomas Short-Term Survivors: A POLA Network Study |
title_full | Characteristics of Anaplastic Oligodendrogliomas Short-Term Survivors: A POLA Network Study |
title_fullStr | Characteristics of Anaplastic Oligodendrogliomas Short-Term Survivors: A POLA Network Study |
title_full_unstemmed | Characteristics of Anaplastic Oligodendrogliomas Short-Term Survivors: A POLA Network Study |
title_short | Characteristics of Anaplastic Oligodendrogliomas Short-Term Survivors: A POLA Network Study |
title_sort | characteristics of anaplastic oligodendrogliomas short-term survivors: a pola network study |
topic | Neuro-Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9074983/ https://www.ncbi.nlm.nih.gov/pubmed/35522558 http://dx.doi.org/10.1093/oncolo/oyac023 |
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