Literature DB >> 3512115

Phase I study of cyclohexylamine and lysine salt of mafosfamide.

R Abele, M S Aapro, J M Haefliger, P Alberto.   

Abstract

Mafosfamide is a new oxazaphosphorine that breaks down spontaneously into 4-hydroxy-cyclophosphamide. A phase I trial with cyclohexylamine and lysine salts of mafosfamide was carried out in 16 patients, using weekly IV perfusion. Dose-limiting toxicities were not hematological, but consisted in the development of severe pain along the vein during administration. A particular mucosal syndrome with sneezing and conjunctivitis was seen only after administration of the lysine salt. The dose of 700 mg/m2 per week represents the maximum tolerated dose with this weekly schedule.

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Year:  1986        PMID: 3512115     DOI: 10.1007/bf00256173

Source DB:  PubMed          Journal:  Cancer Chemother Pharmacol        ISSN: 0344-5704            Impact factor:   3.333


  3 in total

1.  Comparative pharmacologic study in vitro and in vivo with cyclophosphamide (NSC-26271), cyclophosphamide metabolites, and plain nitrogen mustard compounds.

Authors:  N Brock
Journal:  Cancer Treat Rep       Date:  1976-04

2.  Experimental toxicology of ASTA Z 7557 (INN mafosfamide).

Authors:  J Pohl; P Hilgard; W Jahn; H J Zechel
Journal:  Invest New Drugs       Date:  1984       Impact factor: 3.850

3.  Antineoplastic activity of ASTA Z 7557 (NSC-345842, INN mafosfamide) on transplantable murine tumors.

Authors:  G Atassi; P Hilgard; J Pohl
Journal:  Invest New Drugs       Date:  1984       Impact factor: 3.850

  3 in total
  1 in total

Review 1.  Bone marrow purging with mafosfamide--a critical survey.

Authors:  H Sindermann; M Peukert; P Hilgard
Journal:  Blut       Date:  1989-11
  1 in total

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