Literature DB >> 8431974

Phase I clinical study of LL-D49194 alpha 1 with retrospective pharmacokinetic investigations in mice and humans. The EORTC ECTG.

J Cassidy1, M A Graham, W Ten Bokkel Huinink, C McDaniel, A Setanoians, E M Rankin, D J Kerr, S B Kaye.   

Abstract

LL-D49194 alpha 1 is a new cytotoxic antibiotic selected for clinical phase I study because of its impressive pre-clinical anti-tumour activity and its low toxicity profile in experimental animals. A total of 15 patients were treated in centres in Glasgow and Amsterdam at doses ranging from 0.25 to 4 mg/m2. One minor response was noted in a patient with colonic carcinoma. The study was suspended following the discovery of unexpected cardiotoxicity. As this toxicity was not consistent with the standard (EORTC) European Organisation for Research and Treatment of Cancer toxicology profile, we chose to investigate the pharmacokinetics of LL-D49194 alpha 1 in mice and humans in more detail to try to explain this phenomenon. A major difference in plasma protein binding was discovered between mice and patients, with a suggestion of non-linear kinetics being noted at higher doses in humans. It is likely that these differences in drug handling account for the unexpected and serious toxicity encountered in this trial.

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 8431974     DOI: 10.1007/bf00686154

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


  3 in total

1.  The pharmacokinetics and toxicity of the anthrapyrazole anti-cancer drug CI-941 in the mouse: a guide for rational dose escalation in patients.

Authors:  M A Graham; D R Newell; B J Foster; A H Calvert
Journal:  Cancer Chemother Pharmacol       Date:  1989       Impact factor: 3.333

2.  Pharmacokinetically guided dose escalation in phase I clinical trials. Commentary and proposed guidelines. EORTC Pharmacokinetics and Metabolism Group.

Authors: 
Journal:  Eur J Cancer Clin Oncol       Date:  1987-07

3.  Preclinical and phase I studies with rhizoxin to apply a pharmacokinetically guided dose-escalation scheme.

Authors:  M A Graham; D Bissett; A Setanoians; T Hamilton; D J Kerr; R Henrar; S B Kaye
Journal:  J Natl Cancer Inst       Date:  1992-04-01       Impact factor: 13.506

  3 in total
  1 in total

1.  Component-based syntheses of trioxacarcin A, DC-45-A1 and structural analogues.

Authors:  Thomas Magauer; Daniel J Smaltz; Andrew G Myers
Journal:  Nat Chem       Date:  2013-09-08       Impact factor: 24.427

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.