A Phase II Study of KRN8602(MX2), a Novel Morpholino Anthracycline Derivative,in Patients with Recurrent Malignant Glioma |
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Authors: | Kuratsu Jun-Ichi Arita Norio Kurisu Kaoru Uozumi Toru Hayakawa Toru Ushio Yukitaka |
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Institution: | (1) Department of Neurosurgery, Faculty of Medicine, Kagoshima University, Kagoshima;(2) Department of Neurosurgery, Osaka University Medical School, Osaka;(3) Department of Neurosurgery, Hiroshima University, School of Medicine, Hiroshima;(4) Department of Neurosurgery, Hiroshima Prefectural Hospital, Hiroshima;(5) Department of Neurosurgery, Kumamoto University, School of Medicine, Kumamoto |
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Abstract: | KRN8602(MX2) is a newly developed morpholino-anthracycline that has been found to cross the blood–brain barrier and be distributed in brain tissue after intravenous administration and to be effective against human glioma cells and the intracerebrally transplanted tumors in vivo. In order to confirm these promising preclinical observations clinically, we performed a phase II trial of KRN8602 in patients with recurrent malignant glioma.The 44 patients enrolled received at least 2 cycles of KRN8602 35 mg/m2/day at 3–4 week intervals by intravenous bolus. Of the 44 patients, 37 could be evaluated for response, and 39 for toxicity. One patient with anaplastic astrocytoma had a complete response (1/37, 3%), and 2 patients with anaplastic astrocytoma and 1 with brain stem glioma had a partial response (3/37, 8%). The overall response rate was 11% (4/37). All patients who responded had received prior chemotherapy that included nitrosoureas. No response was observed in the patients with glioblastoma.Myelosuppression was moderately severe, with 72% of patients developing grade 3 or 4 leukopenia. Severe nausea/vomiting was observed in 31% of the patients. No severe cardiotoxicity was observed.The results indicate that KRN8602 has modest activity against recurrent malignant glioma with relatively severe, but manageable toxicity. It seems to be worthwhile to further assess the efficacy and toxicity of KRN8602 against malignant glioma, which is generally less sensitive to chemotherapy. |
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Keywords: | malignant glioma chemotherapy anthracyclines KRN8602(MX2) phase II study |
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