Lost in third space: altered tyrosine-kinase inhibitor pharmacokinetics in a patient with malignant ascites

Cancer Chemother Pharmacol. 2022 Feb;89(2):271-274. doi: 10.1007/s00280-021-04377-0. Epub 2021 Dec 1.

Abstract

Background: Pazopanib and sunitinib are oral tyrosine kinase inhibitors (TKI) approved for the treatment of renal cell carcinoma. For both oncolytics, a clear target trough concentration level in plasma has been defined above which improved clinical efficacy can be expected. However, many factors can alter TKI exposure, including disease characteristics.

Case: A 79-year old male with metastatic papillary renal cell carcinoma and malignant ascites was treated with pazopanib. Initially, treatment with pazopanib at adequate trough concentrations resulted in regression of ascites. After a 6-month puncture-free interval, paracenteses were again required and the plasma trough concentration of pazopanib had decreased to 5 mg/L without any dose adjustments. Despite a dose increase, pazopanib levels remained subtherapeutic and could not prevent new paracenteses. Pazopanib concentrations in the drained ascites fluid were comparable to plasma concentrations and remained high also after treatment discontinuation. This observation suggests that the ascites compartment may act as a third space in which pazopanib accumulates. During subsequent treatment with sunitinib, a similar distribution over ascites fluid was observed.

Conclusion: Presence of ascites or pleural effusion in patients treated with TKIs may lead to subtherapeutic plasma exposure, which may hamper treatment efficacy. Measuring TKIs plasma concentrations regularly during treatment is essential to identify patients with subtherapeutic exposure.

Keywords: Exposure; Malignant ascites; Pazopanib; Pharmacokinetics; Sunitinib.

Publication types

  • Case Reports

MeSH terms

  • Aged
  • Ascites / drug therapy*
  • Carcinoma, Renal Cell / drug therapy*
  • Carcinoma, Renal Cell / pathology
  • Dose-Response Relationship, Drug
  • Humans
  • Indazoles / administration & dosage
  • Indazoles / pharmacokinetics
  • Kidney Neoplasms / drug therapy*
  • Kidney Neoplasms / pathology
  • Male
  • Protein Kinase Inhibitors / administration & dosage
  • Protein Kinase Inhibitors / pharmacokinetics*
  • Pyrimidines / administration & dosage
  • Pyrimidines / pharmacokinetics
  • Sulfonamides / administration & dosage
  • Sulfonamides / pharmacokinetics
  • Sunitinib / administration & dosage
  • Sunitinib / pharmacokinetics
  • Treatment Outcome

Substances

  • Indazoles
  • Protein Kinase Inhibitors
  • Pyrimidines
  • Sulfonamides
  • pazopanib
  • Sunitinib