Simultaneous boost radiotherapy versus conventional dose radiotherapy for patients with newly diagnosed glioblastoma: a multi-institutional analysis

Author:

Takano Seiya,Tomita NatsuoORCID,Kuno Mayu,Niwa Masanari,Torii Akira,Takaoka Taiki,Kita Nozomi,Okazaki Dai,Yamamoto Shintaro,Kawai Tatsuya,Sugie Chikao,Ogawa Yasutaka,Matsumoto Kenichi,Uchiyama Kaoru,Otsuka Shinya,Matsui Tooru,Miyakawa Akifumi,Mizuno Tomoki,Iida Masato,Tanikawa Motoki,Mase Mitsuhito,Hiwatashi Akio

Abstract

AbstractWe compared survival outcomes of high-dose concomitant boost radiotherapy (HDCBRT) and conventional dose radiotherapy (CRT) for newly diagnosed glioblastoma (GB). Patients treated with intensity-modulated radiation therapy for newly diagnosed GB were included. In HDCBRT, specific targets received 69, 60, and 51 Gy in 30 fractions, while 60 Gy in 30 fractions was administered with a standard radiotherapy method in CRT. Overall survival (OS) and progression-free survival (PFS) were compared using the Log-rank test, followed by multivariate Cox analysis. The inverse probability of treatment weighting (IPTW) method was also applied to each analysis. Among 102 eligible patients, 45 received HDCBRT and 57 received CRT. With a median follow-up of 16 months, the median survival times of OS and PFS were 21 and 9 months, respectively. No significant differences were observed in OS or PFS in the Kaplan–Meier analyses. In the multivariate analysis, HDCBRT correlated with improved OS (hazard ratio, 0.49; 95% confidence interval, 0.27–0.90; P = 0.021), and this result remained consistent after IPTW adjustments (P = 0.028). Conversely, dose suppression due to the proximity of normal tissues and IMRT field correlated with worse OS and PFS (P = 0.008 and 0.049, respectively). A prospective study with a stricter protocol is warranted to validate the efficacy of HDCBRT for GB.

Funder

Grant-in-Aid for Research in Nagoya City University

Publisher

Springer Science and Business Media LLC

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