Imaging biological activity of a glioblastoma treated with an individual patient-tailored, experimental therapy regimen

J Neurooncol. 2009 Jul;93(3):425-30. doi: 10.1007/s11060-008-9790-3. Epub 2009 Jan 29.

Abstract

Purpose: To monitor the metabolic effects of an individual patient-tailored, experimental glioma therapy regimen that included repetitive multiple neurosurgical resections, radiosurgical interventions, and an adjuvant maintenance therapy based on the tyrosine kinase inhibitor imatinib in combination with the chemotherapeutic agent hydroxyurea (HU).

Procedures: Therapeutic effects were monitored in a 26-year-old male patient with a glioblastoma multiforme by multimodal imaging using sequential L: -[methyl-(11)C]-methionine positron emission tomography (MET-PET) and MRI. The normalized MET uptake and volume of the metabolically active tumor were assessed sequentially.

Results: The individual patient-tailored, experimental glioma therapy caused a continuous decline of metabolically active tumor volume, associated with clinical remission over a period of more than two years.

Conclusions: MET-PET seems to be useful for monitoring patient-tailored, experimental glioma therapy regimens, especially when patients are treated with a multi-step therapeutic regimen. Monitoring and guidance of those experimental therapy regimens by MET-PET in a larger patient group are needed to confirm its clinical value.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Benzamides
  • Brain Neoplasms / diagnostic imaging*
  • Brain Neoplasms / therapy*
  • Combined Modality Therapy
  • Cranial Irradiation
  • Glioblastoma / diagnostic imaging*
  • Glioblastoma / therapy*
  • Humans
  • Hydroxyurea / administration & dosage
  • Imatinib Mesylate
  • Male
  • Neurosurgical Procedures
  • Piperazines / administration & dosage
  • Positron-Emission Tomography
  • Pyrimidines / administration & dosage

Substances

  • Benzamides
  • Piperazines
  • Pyrimidines
  • Imatinib Mesylate
  • Hydroxyurea