Phase I trial of intrapleural docetaxel administered through an implantable catheter in subjects with a malignant pleural effusion. Academic Article uri icon

Overview

abstract

  • INTRODUCTION: Malignant pleural effusion (MPE) is a common complication in patients with advanced malignancy. This dose escalation phase I study was designed to determine the maximum tolerated dose of intrapleural docetaxel administered through an implantable catheter in subjects with MPE. METHODS: Subjects with MPE (n = 15) with median age of 64.6 years and an Eastern Cooperative Oncology Group performance status of 0 to 2 at baseline were enrolled into four single dose levels of docetaxel administered intrapleurally after drainage of the pleural effusion and insertion of an intrapleural catheter. The study determined the pharmacokinetic properties, clinical response, and toxicity profile of intrapleural docetaxel. RESULTS: All patients tolerated the therapy well and there were no significant toxicities. The majority of patients had a complete radiographic response. All patients receiving dose 100 mg/m2 or higher had a complete radiographic response. One dose-limiting toxicity was encountered in the dose 50 mg/m2. Pharmacokinetic data demonstrated peak plasma concentration of docetaxel between 30 minutes and 6 hours after infusion. Pleural exposure to docetaxel was 1000 times higher than systemic exposure. CONCLUSIONS: Single-dose intrapleural administration of doxetaxel is well tolerated in patients with MPE with minimal toxicity. The excellent clinical responses in this study after treatment with intrapleural doxetaxel suggest that further investigation is warranted.

authors

  • Jones, David
  • Taylor, Matthew D
  • Petroni, Gina R
  • Shu, Jianfen
  • Burks, Sandra G
  • Daniel, Thomas M
  • Gillenwater, Heidi H

publication date

  • January 1, 2010

Research

keywords

  • Antineoplastic Agents
  • Catheters, Indwelling
  • Pleural Effusion, Malignant
  • Taxoids

Identity

Scopus Document Identifier

  • 76149141215

Digital Object Identifier (DOI)

  • 10.1097/JTO.0b013e3181c07ddc

PubMed ID

  • 19884858

Additional Document Info

volume

  • 5

issue

  • 1