D32 D33.3 D35.2
Conditions
Interventions
Group 1: Patients who have undergone radiotherapy, either as adjuvant or definitive treatment, for meningiomas, acoustic neuromas, or other benign neoplasms located in the brain are included in this s
Sponsors
LMU Klinikum, Klinik und Poliklinik für Strahlentherapie und Radioonkologie
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: ? Definitive or postoperative percutaneous radiotherapy ? Radiotherapeutic treatment of a benign neoplasm in the brain
Exclusion criteria
Exclusion criteria: Age < 18 years
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary objective is to analyze the extent of the radiation fields (especially planning target volume (PTV)), compare it among the different patient cases and correlate it with the survival data (e.g. overall survival (OS) or local control (LC)). | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary objectives include the recording of side effects such as the frequency of cerebral edema and radionecrosis and comparison with the dose distribution. To this end, an analysis of the radiation exposure of the organs at risk (e.g. brain, brain stem, optic nerves) and quality control with the corresponding constraints will be carried out. In addition, an analysis of the different irradiation techniques (e.g. 3D plan, VMAT) will be carried out and, in particular, the side effect profiles and the failure rate will be considered. | — |
Countries
Germany
Contacts
Public ContactSebastian Maier
LMU Klinikum, Klinik und Poliklinik für Strahlentherapie und Radioonkologie
Outcome results
None listed