Phase I and pharmacokinetic study of photodynamic therapy for high-grade gliomas using a novel boronated porphyrin

J Clin Oncol. 2001 Jan 15;19(2):519-24. doi: 10.1200/JCO.2001.19.2.519.

Abstract

Purpose: To determine the recommended dose, toxicity profile, and pharmacokinetics of a novel boronated porphyrin (BOPP) for photodynamic therapy (PDT) of intracranial tumors.

Patients and methods: BOPP was administered alone in increasing doses (0.25, 0.5, 1.0, 2.0, 4.0, or 8.0 mg/kg) preoperatively in patients with intracranial tumors undergoing postresection PDT until dose-limiting toxicity (DLT) was observed.

Results: Twenty-nine assessable patients with intracranial tumors received BOPP intravenously 24 hours before surgery. The recommended dose was 4 mg/kg. Dose escalation was limited by thrombocytopenia. The most common nonhematologic toxicity was skin photosensitivity. Pharmacokinetic parameters showed increased area under the plasma concentration-time curve and maximum concentration with increased dose. Tumor BOPP concentrations also increased with increased dose.

Conclusion: BOPP at a dose of 4 mg/kg was well tolerated. DLT was thrombocytopenia, and photosensitivity was the only other toxicity of note. The efficacy of PDT using BOPP requires further exploration.

Publication types

  • Clinical Trial
  • Clinical Trial, Phase I

MeSH terms

  • Adult
  • Aged
  • Area Under Curve
  • Brain Neoplasms / drug therapy*
  • Drug Administration Schedule
  • Female
  • Glioblastoma / drug therapy*
  • Humans
  • Male
  • Middle Aged
  • Photochemotherapy*
  • Protoporphyrins / pharmacokinetics
  • Protoporphyrins / therapeutic use*
  • Radiation-Sensitizing Agents / pharmacokinetics
  • Radiation-Sensitizing Agents / therapeutic use*
  • Tissue Distribution

Substances

  • Protoporphyrins
  • Radiation-Sensitizing Agents
  • boron protoporphyrin