Viewing Study NCT06180434



Ignite Creation Date: 2024-05-06 @ 7:55 PM
Last Modification Date: 2024-10-26 @ 3:16 PM
Study NCT ID: NCT06180434
Status: RECRUITING
Last Update Posted: 2023-12-22
First Post: 2023-12-12

Brief Title: Short Term Outcomes After PRoton and PhotoN RadiOtherapy for IDH Mutated Grade 2 and 3 Gliomas
Sponsor: Erasmus Medical Center
Organization: Erasmus Medical Center

Study Overview

Official Title: Short Term Outcomes After PRoton and PhotoN RadiOtherapy for IDH Mutated Grade 2 and 3 Gliomas
Status: RECRUITING
Status Verified Date: 2024-10
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: SOPRANO
Brief Summary: Rationale

Proton beam therapy has recently become available for the treatment of patients with WHO grade 2 and 3 IDH mutated IDHmt glioma in the Netherlands The dose distributions associated with proton therapy have substantially reduced the volume of the normal brain irradiated with low and intermediate radiotherapy doses Whether this impacts rates of progressive disease or safety issues and how this compares with a similar population treated with photon therapy is currently unknown

Objective

To investigate short term outcomes after proton and photon radiotherapy for grade 2 and 3 IDHmt glioma
Detailed Description: Patients with grade 2 and 3 IDHmt glioma treated with proton therapy in Holland PTC Maastro and UMC Groningen and referred Erasmus MC Haaglanden MC LUMC Amsterdam UMC Verbeeten Institute Maastro UMC Groningen and Leuven University Hospital between 1st of January 2018 and the 30th of June 2022 The outcomes will be compared to those from patients with grade 2 and 3 IDHmt glioma treated with photon therapy in the same institutes and during the same period of time The applied clinical target volume CTV margins and the chemotherapy are preferably similar for proton and photon therapy

Retrospective data will be collected from the electronic records of each participating institute For the primary outcome data will be collected on interventions radiotherapy surgery chemotherapy medication for either tumor progression or toxicity after radiotherapy This will be used to calculate next intervention free survival as primary outcome

For the secondary outcomes data on survival disease progression pseudoprogression and toxicity will be used to calculate overall survival progression free survival and pseudoprogression free survival as well as toxicity incidence

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None