Effects of levamisole (NSC-177023) and tetramisole (NSC-102063) in experimental tumor systems.

Cancer chemotherapy reports Pub Date : 1975-07-01
R K Johnson, D P Houchens, M R Gaston, A Goldin
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Abstract

Levamisole and tetramisole had no antitumor effect against the following transplantable syngeneic murine tumors: L1210 leukemia, P388 leukemia, B16 melanoma, Madison 109 lung tumor, and Lewis lung carcinoma. In the Lewis lung carcinoma system there was no effect on primary tumor growth, metastasis, or survival. Tetramisole had a variable effect on the growth of rhabdomyosarcomas and the survival of BALB/c mice following intramuscular inoculation of Moloney sarcoma virus. In two experiments treatment with tetramisole either prior to or following inoculation of Moloney sarcoma virus increased the number of mice with tumor regression as opposed to progressive tumor growth, incrneased the number of long-term survivors, and prolonged the lifespan of mice that died of tumor. In two further tests neither levamisole nor tetramisole had an effect in this system. In mice immunosuppressed with cyclophosphamide prior to virus inoculation, there was not effect of treatment with levamisole or tetramisole.

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左旋咪唑(NSC-177023)和四曲咪唑(NSC-102063)在实验性肿瘤系统中的作用。
左旋咪唑和四曲咪唑对L1210白血病、P388白血病、B16黑色素瘤、Madison 109肺癌和Lewis肺癌等可移植的同基因小鼠肿瘤无抗肿瘤作用。在Lewis肺癌系统中,对原发肿瘤的生长、转移或生存没有影响。四曲咪唑对肌肉注射莫洛尼肉瘤病毒后横纹肌肉瘤的生长和BALB/c小鼠的存活有不同的影响。在两项实验中,在接种莫洛尼肉瘤病毒之前或之后用四咪唑治疗,增加了肿瘤消退(而不是肿瘤进行性生长)的小鼠数量,增加了长期幸存者的数量,延长了死于肿瘤的小鼠的寿命。在进一步的两项试验中,左旋咪唑和四咪唑对该系统均无影响。在病毒接种前用环磷酰胺免疫抑制的小鼠中,用左旋咪唑或四曲咪唑治疗没有效果。
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PORFIROMYCIN. Phase I study of 5-azacytidine (NSC-102816) using 24-hour continuous infusion for 5 days. Bleomycin (NSC-125066) and CCNU (NSC-79037) in the combination chemotherapy of mopp-resistant hodgkin's disease. Combination chemotherapy with 5-fluorouracil (NSC-19893), methotrexate (NSC-740), and prednisolone (NSC-9900) (FAP protocol) for hepatoma. Cyclophosphamide (NSC-26271) maintenance therapy after a second remission of childhood acute lymphoblastic leukemia: comparative clinical trial (standard dose versus intermittent high dose versus cyclophosphamide plus cytosine arabinoside (NSC-63878)).
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