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Untersuchungen Zur Verlaufskontrolle Bei Re-Bestrahlung Von Glioblastompatienten Mittels Kombinierter [18F]FET-PET-Kernspintomographie


N/A
18 Years
75 Years
Open (Enrolling)
Both
Glioblastoma, Nervous System Neoplasms, Central Nervous System Neoplasms, Astrocytoma, Glioma, Neoplasms, Neuroepithelial, Neuroectodermal Tumors, Neoplasms by Histologic Type, Neoplasms, Nerve Tissue

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Trial Information

Untersuchungen Zur Verlaufskontrolle Bei Re-Bestrahlung Von Glioblastompatienten Mittels Kombinierter [18F]FET-PET-Kernspintomographie


For glioblastoma (GBM) patients it has been proven that a [18F]FET-PET scan is very helpful
especially in target volume definition and after the treatment, in turn, the combination of
MRI and [18F]FET-PET is diagnostically most useful to distinguish between radiation necrosis
and a real progressive disease.

The response to therapy is based on the newly formulated Revised Assessment in
Neuro-Oncology (RANO) criteria. Kinetic and static [18F]FET-PET scans are useful to
supplement this modality and its own prognostic value concerning relapsing patients will be
examined.

The special feature of this study is the use of both modalities in parallel, allowing
simultaneous acquisition of morphological changes, functional and molecular imaging.

Secondary methodological issues are dealt with, such as the relationship between contrast
uptake, perfusion and [18F]FET uptake. In this regard, the hybrid imaging may serve for
hypothesis generation, as in parallel in a unique way of contrast enhancement and tracer
kinetics can be investigated (simultaneous contrast-enhanced analysis and tracer
application).

In particular, FET kinetics are examined in more detail (for example, differences between
increasing and decreasing kinetics) to find ways of how to use certain MRI sequences for
better visualization of viable tumor tissue and vice versa .


Inclusion Criteria:



- 18 - 75 years old

- histologically or magnetic resonance imaging proven recurrent glioblastoma

- re-irradiation possible

- willing and able to give free informed consent

Exclusion Criteria:

- not willing or able to give free informed consent

- pregnancy

- claustrophobia

- metallic objects or implanted medical devices in the body

Type of Study:

Observational

Study Design:

Observational Model: Cohort, Time Perspective: Prospective

Principal Investigator

Maximilian Niyazi, MD, MSc

Investigator Role:

Principal Investigator

Investigator Affiliation:

Ludwig-Maximilians - University of Munich

Authority:

Germany: Federal Institute for Drugs and Medical Devices

Study ID:

361-11

NCT ID:

NCT01579253

Start Date:

April 2012

Completion Date:

Related Keywords:

  • Glioblastoma
  • Nervous System Neoplasms
  • Central Nervous System Neoplasms
  • Astrocytoma
  • Glioma
  • Neoplasms, Neuroepithelial
  • Neuroectodermal Tumors
  • Neoplasms by Histologic Type
  • Neoplasms, Nerve Tissue
  • Recurrent glioblastoma
  • Radiotherapy
  • PET-MRI
  • FET-PET
  • Astrocytoma
  • Neoplasms
  • Glioblastoma
  • Glioma
  • Neoplasms by Histologic Type
  • Neoplasms, Nerve Tissue
  • Nervous System Neoplasms
  • Central Nervous System Neoplasms
  • Neuroectodermal Tumors
  • Neoplasms, Neuroepithelial

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