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ACT-16 THE POTENTIAL OF HYPOFRACTIONATED RADIOTHERAPY AND BEVACIZUMAB FOR GLIOBLASTOMA TREATMENT

INTRODUCTION: First-line bevacizumab (BEV) is now available as a treatment option for glioblastoma (GBM) patients with severe clinical conditions in Japan. However, the survival benefits remain controversial. As we have emphasized the combined effect of BEV and radiation therapy, the strategies; 1)...

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Autores principales: Hata, Nobuhiro, Mizoguchi, Masahiro, Kuga, Daisuke, Hatae, Ryusuke, Sangatsuda, Yuhei, Akagi, Yojiro, Amemiya, Takeo, Fujioka, Yutaka, Takigawa, Kosuke, Yoshitake, Tadamasa, Yoshimoto, Koji, Iihara, Koji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7213105/
http://dx.doi.org/10.1093/noajnl/vdz039.065
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author Hata, Nobuhiro
Mizoguchi, Masahiro
Kuga, Daisuke
Hatae, Ryusuke
Sangatsuda, Yuhei
Akagi, Yojiro
Amemiya, Takeo
Fujioka, Yutaka
Takigawa, Kosuke
Yoshitake, Tadamasa
Yoshimoto, Koji
Iihara, Koji
author_facet Hata, Nobuhiro
Mizoguchi, Masahiro
Kuga, Daisuke
Hatae, Ryusuke
Sangatsuda, Yuhei
Akagi, Yojiro
Amemiya, Takeo
Fujioka, Yutaka
Takigawa, Kosuke
Yoshitake, Tadamasa
Yoshimoto, Koji
Iihara, Koji
author_sort Hata, Nobuhiro
collection PubMed
description INTRODUCTION: First-line bevacizumab (BEV) is now available as a treatment option for glioblastoma (GBM) patients with severe clinical conditions in Japan. However, the survival benefits remain controversial. As we have emphasized the combined effect of BEV and radiation therapy, the strategies; 1) first-line add-on BEV to TMZ-radiation for unresectable GBMs and 2) re-irradiation using IMRT under BEV administration for recurrent GBMs, have been positively applied. To elucidate these potential survival benefits, we retrospectively analyzed survival in GBM patients. METHODS: We analyzed survival in 101 patients with IDH-wild type GBM treated from 2006 to 2018. PFS and OS were assessed in two subgroups (TMZ and TMZ-BEV eras), and the correlations of prognostic factors with survival were evaluated. RESULTS: After BEV approval, OS prolongation tendency (median OS: 14.9 vs. 22.1 months; P = 0.52) was observed, and this tendency was clearer in unresectable cases (10.1 vs 16.1 m P = 0.38). Subanalysis showed a significant prolongation of prognosis in the MGMT unmethylated group (12.2 vs 16.7 m; P = 0.04). In 10 patients of recurrent GBMs receiving BEV combined re-irradiation, adverse events of Grade 3 or higher did not occur. All patients showed PR (N=5) or CR (N=5) after treatment. The mPFS and mOS from the recurrence were 4.3 and 9.4 months, however, no local relapse was observed at their second recurrences. CONCLUSIONS: Our treatment strategy has improved the outcome of high-risk cases after BEV approval. These results implied that hypofractionated radiotherapy under BEV administration might be an efficient treatment protocol as a first-line for high-risk cases, such as after partial excision and MGMT unmethylation.
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spelling pubmed-72131052020-07-07 ACT-16 THE POTENTIAL OF HYPOFRACTIONATED RADIOTHERAPY AND BEVACIZUMAB FOR GLIOBLASTOMA TREATMENT Hata, Nobuhiro Mizoguchi, Masahiro Kuga, Daisuke Hatae, Ryusuke Sangatsuda, Yuhei Akagi, Yojiro Amemiya, Takeo Fujioka, Yutaka Takigawa, Kosuke Yoshitake, Tadamasa Yoshimoto, Koji Iihara, Koji Neurooncol Adv Abstracts INTRODUCTION: First-line bevacizumab (BEV) is now available as a treatment option for glioblastoma (GBM) patients with severe clinical conditions in Japan. However, the survival benefits remain controversial. As we have emphasized the combined effect of BEV and radiation therapy, the strategies; 1) first-line add-on BEV to TMZ-radiation for unresectable GBMs and 2) re-irradiation using IMRT under BEV administration for recurrent GBMs, have been positively applied. To elucidate these potential survival benefits, we retrospectively analyzed survival in GBM patients. METHODS: We analyzed survival in 101 patients with IDH-wild type GBM treated from 2006 to 2018. PFS and OS were assessed in two subgroups (TMZ and TMZ-BEV eras), and the correlations of prognostic factors with survival were evaluated. RESULTS: After BEV approval, OS prolongation tendency (median OS: 14.9 vs. 22.1 months; P = 0.52) was observed, and this tendency was clearer in unresectable cases (10.1 vs 16.1 m P = 0.38). Subanalysis showed a significant prolongation of prognosis in the MGMT unmethylated group (12.2 vs 16.7 m; P = 0.04). In 10 patients of recurrent GBMs receiving BEV combined re-irradiation, adverse events of Grade 3 or higher did not occur. All patients showed PR (N=5) or CR (N=5) after treatment. The mPFS and mOS from the recurrence were 4.3 and 9.4 months, however, no local relapse was observed at their second recurrences. CONCLUSIONS: Our treatment strategy has improved the outcome of high-risk cases after BEV approval. These results implied that hypofractionated radiotherapy under BEV administration might be an efficient treatment protocol as a first-line for high-risk cases, such as after partial excision and MGMT unmethylation. Oxford University Press 2019-12-16 /pmc/articles/PMC7213105/ http://dx.doi.org/10.1093/noajnl/vdz039.065 Text en © The Author(s) 2019. Published by Oxford University Press, the Society for Neuro-Oncology and the European Association of Neuro-Oncology. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://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. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Abstracts
Hata, Nobuhiro
Mizoguchi, Masahiro
Kuga, Daisuke
Hatae, Ryusuke
Sangatsuda, Yuhei
Akagi, Yojiro
Amemiya, Takeo
Fujioka, Yutaka
Takigawa, Kosuke
Yoshitake, Tadamasa
Yoshimoto, Koji
Iihara, Koji
ACT-16 THE POTENTIAL OF HYPOFRACTIONATED RADIOTHERAPY AND BEVACIZUMAB FOR GLIOBLASTOMA TREATMENT
title ACT-16 THE POTENTIAL OF HYPOFRACTIONATED RADIOTHERAPY AND BEVACIZUMAB FOR GLIOBLASTOMA TREATMENT
title_full ACT-16 THE POTENTIAL OF HYPOFRACTIONATED RADIOTHERAPY AND BEVACIZUMAB FOR GLIOBLASTOMA TREATMENT
title_fullStr ACT-16 THE POTENTIAL OF HYPOFRACTIONATED RADIOTHERAPY AND BEVACIZUMAB FOR GLIOBLASTOMA TREATMENT
title_full_unstemmed ACT-16 THE POTENTIAL OF HYPOFRACTIONATED RADIOTHERAPY AND BEVACIZUMAB FOR GLIOBLASTOMA TREATMENT
title_short ACT-16 THE POTENTIAL OF HYPOFRACTIONATED RADIOTHERAPY AND BEVACIZUMAB FOR GLIOBLASTOMA TREATMENT
title_sort act-16 the potential of hypofractionated radiotherapy and bevacizumab for glioblastoma treatment
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7213105/
http://dx.doi.org/10.1093/noajnl/vdz039.065
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