Efficacy of radioactive hypoxia-targeting therapeutic agent 64Cu-ATSM on recurrent malignant glioma: a study protocol for a phase-III, investigator-sponsored, randomized controlled trial

Previously, we conducted the phase I study of 64Cu-ATSM, which is Cu-diacetyl-bis (N4-methylthiosemicarbazone) radiolabeled with Cu-64, for patients with brain tumors and determined the maximum tolerated dose. We started a subsequent multicenter, randomized, open-label phase III study to evaluate the efficacy of 64Cu-ATSM as an investigator-initiated registration-directed trial for recurrent or residual malignant glioma (protocol No. NCCH2301, STEP-64). Patients will be randomized to either the control or study arm (64Cu-ATSM). A large-scale randomized trial seems difficult to perform for patients with brain tumors because of small sample sizes. Therefore, we designed a small randomized trial with 56 patients. Furthermore, as a pragmatic approach in the control arm, physicians can choose treatments depending on the patient's condition among the clinically available options, where the drugs used are not regarded as investigational. The trial was registered in the Japan Registry of Clinical Trials as jRCT2031240090.

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Publication Details

Journal
Japanese Journal of Clinical Oncology
Published
2025-02-27
DOI
https://doi.org/10.1093/jjco/hyaf026
Citations
2
Primary Topic
Glioma Diagnosis and Treatment
Type
article
Field-Weighted Citation Impact
3.25

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article

Efficacy of radioactive hypoxia-targeting therapeutic agent 64Cu-ATSM on recurrent malignant glioma: a study protocol for a phase-III, investigator-sponsored, randomized controlled trial

Taro Shibata, Ryo Sadachi, Shunsuke Yanagisawa, Masako Inaba et al.
2 citations
Japanese Journal of Clinical Oncology
Glioma Diagnosis and Treatment
3.25
article

Efficacy of radioactive hypoxia-targeting therapeutic agent 64Cu-ATSM on recurrent malignant glioma: a study protocol for a phase-III, investigator-sponsored, randomized controlled trial

Taro Shibata, Ryo Sadachi, Shunsuke Yanagisawa, Masako Inaba, Makoto Ohno, Natsuko Okita, Kimiteru Ito, Hiroki Matsumoto, Kenta Anjo, Yoshitaka Narita, Yukari Nagasaka, Kenichi Nakamura, Yukie Yoshii, Yayoi Ando, Hiroaki Kurihara, Masahiko Ichimura
article en
2 citations

Abstract

Previously, we conducted the phase I study of 64Cu-ATSM, which is Cu-diacetyl-bis (N4-methylthiosemicarbazone) radiolabeled with Cu-64, for patients with brain tumors and determined the maximum tolerated dose. We started a subsequent multicenter, randomized, open-label phase III study to evaluate the efficacy of 64Cu-ATSM as an investigator-initiated registration-directed trial for recurrent or residual malignant glioma (protocol No. NCCH2301, STEP-64). Patients will be randomized to either the control or study arm (64Cu-ATSM). A large-scale randomized trial seems difficult to perform for patients with brain tumors because of small sample sizes. Therefore, we designed a small randomized trial with 56 patients. Furthermore, as a pragmatic approach in the control arm, physicians can choose treatments depending on the patient's condition among the clinically available options, where the drugs used are not regarded as investigational. The trial was registered in the Japan Registry of Clinical Trials as jRCT2031240090.

Japanese Journal of Clinical OncologyVol. 55(5)
Kanagawa Prefectural Hospital Organization (JP), National Cancer Centre Japan (JP), National Cancer Center (US), Mizutani Foundation for Glycoscience (JP), Japan Clinical Cancer Research Organization (JP), National Cancer Research Institute (GB), The University of Tokyo (JP)
Japan Agency for Medical Research and Development
Good health and well-being
Openalex Percentile: Top 10%
Glioma Diagnosis and Treatment
3.25
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