PET imaging of multidrug resistance in tumors using 18F-fluoropaclitaxel

Curr Top Med Chem. 2010;10(17):1792-8. doi: 10.2174/156802610792928077.

Abstract

The failure of solid tumors to respond to chemotherapy is a complicated and clinically frustrating issue. The ability to predict which tumors will respond to treatment could reduce the human and monetary costs of cancer therapy by allowing pro-active selection of a chemotherapeutic to which the tumor does not express resistance. PET/CT imaging with a radiolabeled form of paclitaxel, F-18 fluoropaclitaxel (FPAC), may be able to predict the uptake of paclitaxel in solid tumors, and as a substrate of P-glycoprotein, it may also predict which tumors exhibit multidrug resistance (MDR), a phenotype in which tumors fail to respond to a wide variety of chemically unrelated chemotherapeutic agents. This article reviews the synthetic, preclinical and early human data obtained during the development phase of this promising new radiopharmaceutical.

Publication types

  • Review

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / metabolism
  • Drug Resistance, Multiple
  • Drug Resistance, Neoplasm
  • Fluorine Radioisotopes* / chemistry
  • Humans
  • Neoplasms / diagnostic imaging*
  • Neoplasms / drug therapy
  • Paclitaxel / analogs & derivatives*
  • Paclitaxel / chemical synthesis
  • Paclitaxel / chemistry
  • Positron-Emission Tomography*

Substances

  • ATP Binding Cassette Transporter, Subfamily B, Member 1
  • Fluorine Radioisotopes
  • 4-fluoropaclitaxel
  • Paclitaxel