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Physiological MRI for precision radiotherapy of IDH-wildtype glioblastoma

Conditions
brain tumor
glioblastoma
10029211
Registration Number
NL-OMON51604
Lead Sponsor
Erasmus MC, Universitair Medisch Centrum Rotterdam
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Not specified
Target Recruitment
10
Inclusion Criteria

• Informed consent;
• Adults (18 years or older);
• diagnosed with IDH-wildtype GBM, as confirmed by pathology including
molecular analysis post resection/biopsy;
• referred to outpatient clinic of the Department of Radiotherapy to undergo
standard treatment with high-dose RT.
• Patients eligible for 30x2Gy or 15x2.67Gy

Exclusion Criteria

• Contraindication for MRI
• Contraindication for use of gadolinium-based contrast agent (i.e. subject
having renal deficiency)
• Unable to give informed consent

Study & Design

Study Type
Observational invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>Equal prediction of pattern of failure (locations of tumour recurrence) based<br /><br>on the physiological CTV compared to the standard CTV used for radiotherapy<br /><br>planning, with the physiological CTV being smaller in volume. </p><br>
Secondary Outcome Measures
NameTimeMethod
<p>NA</p><br>
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