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Seizure reduction is a prognostic marker in low-grade glioma patients treated with temozolomide

We aimed to analyze the value of seizure reduction and radiological response as prognostic markers of survival in patients with low-grade glioma (LGG) treated with temozolomide (TMZ) chemotherapy. We retrospectively reviewed adult patients with a progressive LGG and uncontrolled epilepsy in two hosp...

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Autores principales: Koekkoek, Johan A. F., Dirven, Linda, Heimans, Jan J., Postma, Tjeerd J., Vos, Maaike J., Reijneveld, Jaap C., Taphoorn, Martin J. B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4718947/
https://www.ncbi.nlm.nih.gov/pubmed/26547911
http://dx.doi.org/10.1007/s11060-015-1975-y
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author Koekkoek, Johan A. F.
Dirven, Linda
Heimans, Jan J.
Postma, Tjeerd J.
Vos, Maaike J.
Reijneveld, Jaap C.
Taphoorn, Martin J. B.
author_facet Koekkoek, Johan A. F.
Dirven, Linda
Heimans, Jan J.
Postma, Tjeerd J.
Vos, Maaike J.
Reijneveld, Jaap C.
Taphoorn, Martin J. B.
author_sort Koekkoek, Johan A. F.
collection PubMed
description We aimed to analyze the value of seizure reduction and radiological response as prognostic markers of survival in patients with low-grade glioma (LGG) treated with temozolomide (TMZ) chemotherapy. We retrospectively reviewed adult patients with a progressive LGG and uncontrolled epilepsy in two hospitals (VUmc Amsterdam; MCH The Hague), who received chemotherapy with TMZ between 2002 and 2014. End points were a ≥50 % seizure reduction and MRI response 6, 12 and 18 months (mo) after the start of TMZ, and their relation with progression-free survival (PFS) and overall survival (OS). We identified 53 patients who met the inclusion criteria. Seizure reduction was an independent prognostic factor for both PFS (HR 0.38; 95 % CI 0.19–0.73; p = 0.004) and OS (HR 0.39; 95 % CI 0.18–0.85; p = 0.018) after 6mo, adjusting for age and histopathological diagnosis, as well as after 12 and 18mo. Patients with an objective radiological response showed a better OS (median 87.5mo; 95 % CI 62.0–112.9) than patients without a response (median 34.4mo; 95 % CI 26.1–42.6; p = 0.046) after 12mo. However, after 6 and 18mo OS was similar in patients with and without a response on MRI. Seizure reduction is an early and consistent prognostic marker for survival after treatment with TMZ, that seems to precede the radiological response. Therefore, seizure reduction may serve as a surrogate marker for tumor response. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11060-015-1975-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-47189472016-01-27 Seizure reduction is a prognostic marker in low-grade glioma patients treated with temozolomide Koekkoek, Johan A. F. Dirven, Linda Heimans, Jan J. Postma, Tjeerd J. Vos, Maaike J. Reijneveld, Jaap C. Taphoorn, Martin J. B. J Neurooncol Clinical Study We aimed to analyze the value of seizure reduction and radiological response as prognostic markers of survival in patients with low-grade glioma (LGG) treated with temozolomide (TMZ) chemotherapy. We retrospectively reviewed adult patients with a progressive LGG and uncontrolled epilepsy in two hospitals (VUmc Amsterdam; MCH The Hague), who received chemotherapy with TMZ between 2002 and 2014. End points were a ≥50 % seizure reduction and MRI response 6, 12 and 18 months (mo) after the start of TMZ, and their relation with progression-free survival (PFS) and overall survival (OS). We identified 53 patients who met the inclusion criteria. Seizure reduction was an independent prognostic factor for both PFS (HR 0.38; 95 % CI 0.19–0.73; p = 0.004) and OS (HR 0.39; 95 % CI 0.18–0.85; p = 0.018) after 6mo, adjusting for age and histopathological diagnosis, as well as after 12 and 18mo. Patients with an objective radiological response showed a better OS (median 87.5mo; 95 % CI 62.0–112.9) than patients without a response (median 34.4mo; 95 % CI 26.1–42.6; p = 0.046) after 12mo. However, after 6 and 18mo OS was similar in patients with and without a response on MRI. Seizure reduction is an early and consistent prognostic marker for survival after treatment with TMZ, that seems to precede the radiological response. Therefore, seizure reduction may serve as a surrogate marker for tumor response. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11060-015-1975-y) contains supplementary material, which is available to authorized users. Springer US 2015-11-07 2016 /pmc/articles/PMC4718947/ /pubmed/26547911 http://dx.doi.org/10.1007/s11060-015-1975-y Text en © The Author(s) 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Clinical Study
Koekkoek, Johan A. F.
Dirven, Linda
Heimans, Jan J.
Postma, Tjeerd J.
Vos, Maaike J.
Reijneveld, Jaap C.
Taphoorn, Martin J. B.
Seizure reduction is a prognostic marker in low-grade glioma patients treated with temozolomide
title Seizure reduction is a prognostic marker in low-grade glioma patients treated with temozolomide
title_full Seizure reduction is a prognostic marker in low-grade glioma patients treated with temozolomide
title_fullStr Seizure reduction is a prognostic marker in low-grade glioma patients treated with temozolomide
title_full_unstemmed Seizure reduction is a prognostic marker in low-grade glioma patients treated with temozolomide
title_short Seizure reduction is a prognostic marker in low-grade glioma patients treated with temozolomide
title_sort seizure reduction is a prognostic marker in low-grade glioma patients treated with temozolomide
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4718947/
https://www.ncbi.nlm.nih.gov/pubmed/26547911
http://dx.doi.org/10.1007/s11060-015-1975-y
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