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Hitting the Mark: Introducing state-of-the-art MRI for precision radiotherapy of glioblastoma

Hitting the Mark: Introducing state-of-the-art MRI for precision radiotherapy of glioblastoma - MOSAIC

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON55947
Enrollment
36
Registered
2023-07-28
Start date
2024-01-03
Completion date
Unknown
Last updated
2025-09-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

brain tumor glioblastoma

Interventions

Four advanced MRI techniques (qBOLD, ASL, DSC and CEST) will be investigated in this research. These techniques provide information on various biological aspects. qBOLD in combination with ASL provide

Sponsors

Erasmus MC, Universitair Medisch Centrum Rotterdam
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

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

MeasureTime 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

MeasureTime 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

Public ContactA.M. Mendez Romero

Erasmus MC, Universitair Medisch Centrum Rotterdam

a.mendezromero@erasmusmc.nl0107035792

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)