Systemic exposure of oxaliplatin and docetaxel in gastric cancer patients with peritonitis carcinomatosis treated with intraperitoneal hyperthermic chemotherapy

W J Koemans, R T van der Kaaij, E C E Wassenaar, C Grootscholten, H Boot, D Boerma, M Los, O Imhof, J H M Schellens, H Rosing, A D R Huitema, J W van Sandick

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

In the PERISCOPE I study, gastric cancer patients with limited peritoneal dissemination were treated with systemic chemotherapy followed by (sub)total gastrectomy, cytoreductive surgery and hyperthermic intraperitoneal chemotherapy (HIPEC) with 460 mg/m2 hyperthermic oxaliplatin followed by normothermic docetaxel in escalating doses (0, 50, 75 mg/m2). In total, 25 patients completed the study protocol. Plasma samples were collected before the start of the HIPEC procedure, after oxaliplatin washing, after docetaxel washing and the following morning. Median peak plasma concentrations were 5.5∗10-3 mg/ml for oxaliplatin, 89∗10-6 mg/ml for docetaxel (dose 50 mg/m2) and 113∗10-6 mg/ml for docetacel (dose 75 mg/m2). The following morning median plasma concentrations were 32% and 4% of the measured peak concentrations for oxaliplatin and docetaxel, respectively. For both cytostatic agents, no correlation was found between intraperitoneal fluid concentration and peak plasma concentration. High doses oxaliplatin and docetaxel can be given intraperitoneally without causing potentially toxic systemic concentrations.

Original languageEnglish
Pages (from-to)486-489
Number of pages4
JournalEuropean Journal of Surgical Oncology
Volume47
Issue number2
Early online date5 Aug 2020
DOIs
Publication statusPublished - Feb 2021

Keywords

  • Docetaxel
  • Gastric cancer
  • Hyperthermic intraperitoneal chemotherapy
  • Oxaliplatin
  • Perfusion
  • Plasma concentration

Fingerprint

Dive into the research topics of 'Systemic exposure of oxaliplatin and docetaxel in gastric cancer patients with peritonitis carcinomatosis treated with intraperitoneal hyperthermic chemotherapy'. Together they form a unique fingerprint.

Cite this