Accelerator-based BNCT for patients with recurrent glioblastoma: a multicenter phase II study

Author:

Kawabata Shinji1ORCID,Suzuki Minoru2,Hirose Katsumi3ORCID,Tanaka Hiroki2ORCID,Kato Takahiro3,Goto Hiromi4ORCID,Narita Yoshitaka5ORCID,Miyatake Shin-Ichi1ORCID

Affiliation:

1. Department of Neurosurgery, Osaka Medical and Pharmaceutical University, Takatsuki, Osaka, Japan

2. Institute for Integrated Radiation and Nuclear Science, Kyoto University, Kumatori, Osaka, Japan

3. Southern Tohoku BNCT Research Center, Koriyama, Fukushima, Japan

4. Department of Neurosurgery, Southern Tohoku Research Institute for Neuroscience, Koriyama, Fukushima, Japan

5. Department of Neurosurgery and Neuro-Oncology, National Cancer Center Hospital, Chuo-ku, Tokyo, Japan

Abstract

Abstract Background Boron neutron capture therapy (BNCT) utilizes tumor-selective particle radiation. This study aimed to assess the safety and efficacy of accelerator-based BNCT (AB-BNCT) using a cyclotron-based neutron generator (BNCT 30) and 10B-boronophenylalanine (SPM-011) in patients with recurrent malignant glioma (MG) (primarily glioblastoma [GB]). Methods This multi-institutional, open-label, phase II clinical trial involved 27 recurrent MG cases, including 24 GB cases, who were enrolled from February 2016 to June 2018. The study was conducted using the abovementioned AB-BNCT system, with 500 mg/kg SPM-011 (study code: JG002). The patients were bevacizumab-naïve and had recurrent MG after standard treatment. The primary endpoint was the 1-year survival rate, and the secondary endpoints were overall survival (OS) and progression-free survival (PFS). Results were compared to those of a previous Japanese domestic bevacizumab trial for recurrent GB (JO22506). Results The 1-year survival rate and median OS of the recurrent GB cases in this trial were 79.2% (95% CI: 57.0–90.8) and 18.9 months (95% CI: 12.9–not estimable), respectively, whereas those of JO22506 were 34.5% (90% CI: 20.0–49.0) and 10.5 months (95% CI: 8.2–12.4), respectively. The median PFS was 0.9 months (95% CI: 0.8–1.0) by the RANO criteria. The most prominent adverse event was brain edema. Twenty-one of 27 cases were treated with bevacizumab following progressive disease. Conclusions AB-BNCT demonstrated acceptable safety and prolonged survival for recurrent MG. AB-BNCT may increase the risk of brain edema due to re-irradiation for recurrent MG; however, this appears to be controlled well with bevacizumab.

Funder

Stella Pharma Corporation

Sumitomo Heavy Industries, Ltd

Publisher

Oxford University Press (OUP)

Subject

Electrical and Electronic Engineering,Building and Construction

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