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Antineoplastic activity of ASTA Z 7557 (INN mafosfamide) in transplanted and autochthonous experimental rodent tumors.

作者信息

Zeller W J, Berger M R, Matys R, Schuhmacher J

出版信息

Invest New Drugs. 1984;2(2):175-80. doi: 10.1007/BF00232348.

DOI:10.1007/BF00232348
PMID:6469512
Abstract

The antineoplastic activities of ASTA Z 7557 and cyclophosphamide (CPA) were compared in advanced transplanted AKR lymphoma by determining the optimal dose using single dose and twofold applications. Autochthonous DMBA-induced leukemias and MNU-induced mammary carcinomas were treated with fractionated doses over 3 and 5 weeks, respectively. In the respective optimal dosages ASTA Z 7557 exhibited an antitumor effect comparable to that of CPA in all three models. The results obtained by treatment of the autochthonous models indicate that Z 7557 seems to have advantages over CPA in the treatment of malignancies with impaired bone marrow function as for instance acute leukemias and in fractionated dose schedules.

摘要

相似文献

1
Antineoplastic activity of ASTA Z 7557 (INN mafosfamide) in transplanted and autochthonous experimental rodent tumors.
Invest New Drugs. 1984;2(2):175-80. doi: 10.1007/BF00232348.
2
Antineoplastic activity of ASTA Z 7557 (NSC-345842, INN mafosfamide) on transplantable murine tumors.ASTA Z 7557(NSC - 345842,国际非专利药品名称马磷酰胺)对可移植性小鼠肿瘤的抗肿瘤活性。
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本文引用的文献

1
Chemotherapy of autochthonous leukemias induced by 7,12-dimethylbenz(a)anthracene in Long Evans rats.7,12-二甲基苯并(a)蒽诱导的长 Evans 大鼠自发性白血病的化疗
J Cancer Res Clin Oncol. 1980;96(2):157-62. doi: 10.1007/BF00405500.
2
A Ga-68-labeled tetrabromophthalein (Ga-68 BP-IDA) for positron imaging of hepatobiliary function: concise communication.一种用于肝胆功能正电子成像的镓-68标记四溴酚酞(镓-68 BP-IDA):简要通讯
J Nucl Med. 1983 Jul;24(7):593-602.
3
Chemically induced autochthonous tumor models in experimental chemotherapy.
实验性化疗中的化学诱导自发肿瘤模型
Behring Inst Mitt. 1984 May(74):201-8.
4
A comparative study of therapeutic activity, myelotoxicity and DNA damage in the bone marrow of mice after cyclophosphamide and ASTA Z 7557 (INN mafosfamide).环磷酰胺和ASTA Z 7557(国际非专利药品名称:马磷酰胺)对小鼠骨髓治疗活性、骨髓毒性及DNA损伤的比较研究
Invest New Drugs. 1984;2(2):181-6. doi: 10.1007/BF00232349.
5
Induction of leukemia in rat by pulse doses of 7,12-dimethylbenz(a)anthracene.脉冲剂量的7,12-二甲基苯并(a)蒽诱发大鼠白血病
Proc Natl Acad Sci U S A. 1966 Jan;55(1):74-81. doi: 10.1073/pnas.55.1.74.
6
Therapeutic efficacy of cyclophosphamide as a function of its metabolism.环磷酰胺的治疗效果与其代谢的关系。
Cancer Res. 1972 Mar;32(3):535-42.
7
Some studies of the active intermediates formed in the microsomal metabolism of cyclophosphamide and isophosphamide.一些关于环磷酰胺和异环磷酰胺微粒体代谢过程中形成的活性中间体的研究。
Biochem Pharmacol. 1974 Jan 1;23(1):115-29. doi: 10.1016/0006-2952(74)90318-9.
8
Clinical pharmacology of cyclophosphamide.环磷酰胺的临床药理学
Cancer Res. 1973 Feb;33(2):226-33.
9
The effect of phenobarbital on cyclophosphamide antitumor activity.苯巴比妥对环磷酰胺抗肿瘤活性的影响。
Cancer Res. 1976 Aug;36(8):2785-9.