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Analysis of pseudoprogression after proton or photon therapy of 99 patients with low grade and anaplastic glioma()

BACKGROUND AND PURPOSE: Proton therapy is increasingly used to treat primary brain tumors. There is concern for higher rates of pseudoprogression (PsP) after protons compared to photons. The purposes of this study are to compare the rate of PsP after proton vs. photon therapy for grade II and III gl...

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Autores principales: Bronk, Julianna K., Guha-Thakurta, Nandita, Allen, Pamela K., Mahajan, Anita, Grosshans, David R., McGovern, Susan L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5862685/
https://www.ncbi.nlm.nih.gov/pubmed/29594248
http://dx.doi.org/10.1016/j.ctro.2018.01.002
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author Bronk, Julianna K.
Guha-Thakurta, Nandita
Allen, Pamela K.
Mahajan, Anita
Grosshans, David R.
McGovern, Susan L.
author_facet Bronk, Julianna K.
Guha-Thakurta, Nandita
Allen, Pamela K.
Mahajan, Anita
Grosshans, David R.
McGovern, Susan L.
author_sort Bronk, Julianna K.
collection PubMed
description BACKGROUND AND PURPOSE: Proton therapy is increasingly used to treat primary brain tumors. There is concern for higher rates of pseudoprogression (PsP) after protons compared to photons. The purposes of this study are to compare the rate of PsP after proton vs. photon therapy for grade II and III gliomas and to identify factors associated with the development of PsP. MATERIALS AND METHODS: Ninety-nine patients age >18 years with grade II or III glioma treated with photons or protons were retrospectively reviewed. Demographic data, IDH and 1p19q status, and treatment factors were analyzed for association with PsP, progression free survival (PFS), and overall survival (OS). RESULTS: Sixty-five patients were treated with photons and 34 with protons. Among those with oligodendroglioma, PsP developed in 6/42 photon-treated patients (14.3%) and 4/25 proton-treated patients (16%, p = 1.00). Among those with astrocytoma, PsP developed in 3/23 photon-treated patients (13%) and 1/9 proton-treated patients (11.1%, p = 1.00). There was no difference in PsP rate based on radiation type, radiation dose, tumor grade, 1p19q codeletion, or IDH status. PsP occurred earlier in oligodendroglioma patients treated with protons compared to photons, 48 days vs. 131 days, p < .01. On multivariate analyses, gross total resection (p = .03, HR = 0.48, 95%CI = 0.25–0.93) and PsP (p = .04, HR = 0.22, 95% CI = 0.05–0.91) were associated with better PFS; IDH mutation was associated with better OS (p < .01, HR = 0.22, 95%CI = 0.08–0.65). CONCLUSIONS: Patients with oligodendroglioma but not astrocytoma develop PsP earlier after protons compared to photons. PsP was associated with better PFS.
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spelling pubmed-58626852018-03-28 Analysis of pseudoprogression after proton or photon therapy of 99 patients with low grade and anaplastic glioma() Bronk, Julianna K. Guha-Thakurta, Nandita Allen, Pamela K. Mahajan, Anita Grosshans, David R. McGovern, Susan L. Clin Transl Radiat Oncol Article BACKGROUND AND PURPOSE: Proton therapy is increasingly used to treat primary brain tumors. There is concern for higher rates of pseudoprogression (PsP) after protons compared to photons. The purposes of this study are to compare the rate of PsP after proton vs. photon therapy for grade II and III gliomas and to identify factors associated with the development of PsP. MATERIALS AND METHODS: Ninety-nine patients age >18 years with grade II or III glioma treated with photons or protons were retrospectively reviewed. Demographic data, IDH and 1p19q status, and treatment factors were analyzed for association with PsP, progression free survival (PFS), and overall survival (OS). RESULTS: Sixty-five patients were treated with photons and 34 with protons. Among those with oligodendroglioma, PsP developed in 6/42 photon-treated patients (14.3%) and 4/25 proton-treated patients (16%, p = 1.00). Among those with astrocytoma, PsP developed in 3/23 photon-treated patients (13%) and 1/9 proton-treated patients (11.1%, p = 1.00). There was no difference in PsP rate based on radiation type, radiation dose, tumor grade, 1p19q codeletion, or IDH status. PsP occurred earlier in oligodendroglioma patients treated with protons compared to photons, 48 days vs. 131 days, p < .01. On multivariate analyses, gross total resection (p = .03, HR = 0.48, 95%CI = 0.25–0.93) and PsP (p = .04, HR = 0.22, 95% CI = 0.05–0.91) were associated with better PFS; IDH mutation was associated with better OS (p < .01, HR = 0.22, 95%CI = 0.08–0.65). CONCLUSIONS: Patients with oligodendroglioma but not astrocytoma develop PsP earlier after protons compared to photons. PsP was associated with better PFS. Elsevier 2018-01-12 /pmc/articles/PMC5862685/ /pubmed/29594248 http://dx.doi.org/10.1016/j.ctro.2018.01.002 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Bronk, Julianna K.
Guha-Thakurta, Nandita
Allen, Pamela K.
Mahajan, Anita
Grosshans, David R.
McGovern, Susan L.
Analysis of pseudoprogression after proton or photon therapy of 99 patients with low grade and anaplastic glioma()
title Analysis of pseudoprogression after proton or photon therapy of 99 patients with low grade and anaplastic glioma()
title_full Analysis of pseudoprogression after proton or photon therapy of 99 patients with low grade and anaplastic glioma()
title_fullStr Analysis of pseudoprogression after proton or photon therapy of 99 patients with low grade and anaplastic glioma()
title_full_unstemmed Analysis of pseudoprogression after proton or photon therapy of 99 patients with low grade and anaplastic glioma()
title_short Analysis of pseudoprogression after proton or photon therapy of 99 patients with low grade and anaplastic glioma()
title_sort analysis of pseudoprogression after proton or photon therapy of 99 patients with low grade and anaplastic glioma()
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5862685/
https://www.ncbi.nlm.nih.gov/pubmed/29594248
http://dx.doi.org/10.1016/j.ctro.2018.01.002
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