brain tumor glioblastoma
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Written informed consent; Adults (18 years or older); Diagnosed with IDH-wildtype glioblastoma, as confirmed by pathology including molecular analysis post resection/biopsy; Referred to the outpatient clinic of the Dept. of Radiotherapy to undergo standard treatment with radiotherapy (30x2 Gy or 15x2.67 Gy or 10x3.4 Gy);
Exclusion criteria
Exclusion criteria: Contraindication for (3 Tesla) MRI; Contraindication for use of gadolinium-based contrast agent (e.g. subject having renal deficiency or known allergy); Referred for treatment of recurrent glioblastoma; Previous radiotherapy to the brain; Unable to give informed consent;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pattern of failure and dose to organs at risk by the radiotherapy plan based on the 1.5-cm CTV and the theoretical plan created with the CTVbio. | — |
Secondary
| Measure | Time frame |
|---|---|
| • The differences in tumor recurrence coverage and size between the CTVbio (based on all three aMRI-scans) and CTVs based on individual or other combinations of aMRI, i.e. based on two or one aMRI-scan(s). • The difference in mean and maximum signal intensity on the individual aMRI-scans between the tumor recurrence site and the contralateral normal-appearing white matter. | — |
Countries
Netherlands
Contacts
Erasmus MC, Universitair Medisch Centrum Rotterdam