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scopus: 7004449804

Brandely, M.

( M. Brandely)


patient f 60008 level pharmacokinetic cancer study vinorelbine triptolide grade blood 18 mg /m dose level cohort apoptosi concentration administration day 1 number toxicity therapy cycle caspase -3 activity liver activation nf-jb plasma table range liver dysfunction phase fi rst cycle journal treatment infusion subset dose levels analysis european effect cancer 4 5 bioavailability 12 mg /m caspase pharmacokinetic parameters fl ow cytometry activity parameter sample dysfunction lymphocytes lymphocyte subsets monocyte plasma concentrations liver impairment route days 1 aucinf death cohort iii response recherche pierre fabre auc 0–9 h lymphocyte pathway cytokine conversion 0.5 tumour fi gures t 1/2z cancer cells cohorts i increase 7.5 cytotoxic therapy clearance mechanism leukocyte pharmacodynamic chemotherapy




2 Most Recent Publications

Mild to moderate liver dysfunction does not require dose reduction of oral or intravenous vinorelbine: Results of a pharmacokinetic study (Article)
Kitzen, J.J.E.M. Puozzo, C. Jonge, M.J.A. de Brandely, M. Verweij, J.
2010-01-01
Phase I dose-escalation study of F60008, a novel apoptosis inducer, in patients with advanced solid tumours (Article)
Kitzen, J.J.E.M. Jonge, M.J.A. de Lamers, C.H.J. Eskens, F.A.L.M. Biessen, D. van der Doorn, L. van Steeg, J. ter Brandely, M. Puozzo, C. Verweij, J.
2009-07-01