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   <subfield code="a">Preventive effects of interleukin 1 β for ACNU-induced myelosuppression in malignant brain tumors: the experimental and preliminary clinical studies</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Satoshi Tanaka, Sadaharu Tabuchi, Kenji Watanabe, Haruo Takigawa, Keiichi Akatsuka, Hideharu Numata, Yasuo Hokama, Tomokatsu Hori]</subfield>
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   <subfield code="a">Summary: The effect of recombinant human interleukin 1 β (rHuIL-1 β) on myelosuppression induced by 3-[(4-amino-2-methyl-5-pyrimidynyl)methyl]-1-(2-chloroethyl)-1-nitrosourea hydrochloride (ACNU) was studied. In in vivo study using BALB/c mice, pretreatment with 1 µ g/mouse of rHuIL-1 β as a single intraperitoneal (i.p.) injection had a significant preventive effect on thrombocytopenia as well as granulocytopenia induced by ACNU at an intravenous dose of 60 mg/kg. Facilitated recovery by rHuIL-1 β administered seven days after injection of high-dose ACNU was also observed. Experimental combination immunochemotherapy with high-dose ACNU and rHuIL-1 β was performed in nude mice inoculated with human glioblastoma subcutaneously. The elongation of the survival time of the tumor bearing nude mice was also observed in combined use of high dose ACNU with rHuIL-1 β. Seven patients with malignant brain tumors received intravenous 2.5-3 mg/kg ACNU. All patients were subcutaneously injected with 2 × 104-U or more rHuIL-1 β twice a week or daily. The mean nadir of leukocyte, granulocyte, and thrombocyte counts of the 7 patients received 2.5-3 mg/kg ACNU were significantly higher than in matched historical controls. In combination with rHuIL-1 β, it may be possible to use chemotherapeutic agents at a relatively high dose.</subfield>
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