Pharmacokinetics and excretion of 14C-Plitidepsin in patients with advanced cancer

L van Andel*, S Fudio, H Rosing, S Munt, B Miguel-Lillo, I González, M M Tibben, N de Vries, A H M de Vries Schultink, J H M Schellens, J H Beijnen

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Plitidepsin (Aplidin®) is a marine-derived anticancer compound currently investigated in phase III clinical trials. This article describes the distribution, metabolism and excretion of this novel agent and it mainly aims to identify the major routes of elimination. Six subjects were enrolled in a mass balance study during which radiolabelled plitidepsin was administered as a 3-h intravenous infusion. Blood samples were taken and urine and faeces were collected. Total radioactivity (TRA) analysis using Liquid Scintillation Counting (LSC) was done to determine the amount of radioactivity excreted from the body and plitidepsin concentrations in whole blood, plasma and urine were determined by validated liquid chromatography-tandem mass spectrometry (LC-MS/MS) assays. In total, a mean of 77.4% of the administered radioactivity was excreted over a time period of 20 days, of which 71.3% was recovered in faeces and 6.1% was found in urine. The majority excreted in urine was accounted for by unchanged plitidepsin, with only 1.5% of the total administered dose explained by metabolites in urine. Faeces, on the other hand contained low levels of parent compound, which means that most of the TRA excreted in faeces was accounted for by metabolites. TRA levels were 3.7 times higher in whole blood compared to plasma. Plitidepsin was widely distributed and plasma clearance was low. This study shows that red blood cells are a major distribution compartment and that the biliary route is the main route of total radioactivity excretion.

Original languageEnglish
Pages (from-to)589-598
Number of pages10
JournalInvestigational New Drugs
Volume35
Issue number5
DOIs
Publication statusPublished - Oct 2017
Externally publishedYes

Keywords

  • Administration, Oral
  • Aged
  • Carbon Radioisotopes/pharmacokinetics
  • Depsipeptides/pharmacokinetics
  • Feces/chemistry
  • Female
  • Humans
  • Infusions, Intravenous/methods
  • Male
  • Middle Aged
  • Neoplasms/metabolism
  • Peptides, Cyclic
  • Tissue Distribution

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