Feasibility of Salvage Re-irradiation With Stereotactic Radiotherapy for Recurrent Glioma Using CyberKnife.


Journal

Anticancer research
ISSN: 1791-7530
Titre abrégé: Anticancer Res
Pays: Greece
ID NLM: 8102988

Informations de publication

Date de publication:
Jun 2019
Historique:
received: 29 04 2019
revised: 12 05 2019
accepted: 17 05 2019
entrez: 10 6 2019
pubmed: 10 6 2019
medline: 18 6 2019
Statut: ppublish

Résumé

To evaluate the toxicity and efficacy of re-irradiation with salvage stereotactic radiotherapy (SRT) for recurrent glioma using CyberKnife. This study retrospectively investigated 35 patients with 48 recurrent grade 2-4 gliomas who received SRT between 1998 and 2011. Six patients (17.1%) had grade 2 gliomas, nine (25.7%) had grade 3 gliomas, and 20 (57.1%) had glioblastomas; all initially underwent surgery and conventional radiotherapy. The median initial and subsequent radiotherapy doses were 60 and 26 Gy, respectively. After a median follow-up period of 9.0 months, the only toxicity of grade 2 or more was radiation-induced brain necrosis in four patients (11.4%). The median overall and progression-free survival periods following re-irradiation were 9.0 and 3.0 months, respectively. Univariate analysis revealed that performance status at salvage re-irradiation was a significant predictor of progression-free survival. Salvage re-irradiation using CyberKnife is feasible, with an acceptable toxicity profile, for patients with recurrent glioma.

Identifiants

pubmed: 31177132
pii: 39/6/2935
doi: 10.21873/anticanres.13423
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2935-2940

Informations de copyright

Copyright© 2019, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.

Auteurs

Kana Adachi (K)

Department of Radiation Oncology, Toyonaka Municipal Hospital, Toyonaka, Japan.

Kazuhiko Hayashi (K)

Department of Radiation Oncology, Osaka University Graduate School of Medicine, Suita, Japan k.hayashi@osaka-himak.or.jp.
Osaka Heavy Ion Therapy Center, Osaka, Japan.

Naoki Kagawa (N)

Department of Neurosurgery, Osaka University Graduate School of Medicine, Suita, Japan.

Manabu Kinoshita (M)

Department of Neurosurgery, Osaka University Graduate School of Medicine, Suita, Japan.

Iori Sumida (I)

Department of Radiation Oncology, Osaka University Graduate School of Medicine, Suita, Japan.

Yuichi Akino (Y)

Department of Radiation Oncology, Osaka University Graduate School of Medicine, Suita, Japan.

Hiroya Shiomi (H)

Department of Radiation Oncology, Osaka University Graduate School of Medicine, Suita, Japan.

Keisuke Tamari (K)

Department of Radiation Oncology, Osaka University Graduate School of Medicine, Suita, Japan.

Osamu Suzuki (O)

Department of Radiation Oncology, Osaka University Graduate School of Medicine, Suita, Japan.

Ryuichi Hirayama (R)

Department of Neurosurgery, Osaka University Graduate School of Medicine, Suita, Japan.

Noriyuki Kijima (N)

Department of Neurosurgery, Osaka University Graduate School of Medicine, Suita, Japan.

Fumiaki Isohashi (F)

Department of Radiation Oncology, Osaka University Graduate School of Medicine, Suita, Japan.

Yuji Seo (Y)

Department of Radiation Oncology, Osaka University Graduate School of Medicine, Suita, Japan.

Keisuke Otani (K)

Department of Radiation Oncology, Osaka University Graduate School of Medicine, Suita, Japan.

Haruhiko Kishima (H)

Department of Neurosurgery, Osaka University Graduate School of Medicine, Suita, Japan.

Kazuhiko Ogawa (K)

Department of Radiation Oncology, Osaka University Graduate School of Medicine, Suita, Japan.

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Classifications MeSH