Clinical trial · Interventional
UNIty-Based MR-Linac Guided AdapTive RadiothErapy for High GraDe Glioma: a Phase 2 Trial
UNIty-Based MR-Linac Guided AdapTive RadiothErapy for High GraDe Glioma: a Phase 2 Trial (UNITED Trial)
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Glioblastoma (GBM) is a high grade glioma (brain tumor) that is treated with surgery or biopsy followed by radiotherapy (RT) given daily over 3 or 6 weeks with or without an oral chemotherapy. Radiation is targeted to the visible residual tumor on magnetic resonance imaging (MRI) images plus a large margin of 15 to 30 mm to account for possible cancer cells outside the visible tumor and for potential growth or shifts in tumor position throughout the prolonged RT course. Standard RT uses MRI to create a reference plan (with large margins) and treats that same volume every day. This exposes a large amount of healthy brain tissue to radiation leading to toxicity and reduced quality of life. A new technology, the MR-Linac, combines an MRI scanner and a Linac (radiation delivery machine) into one unit. This allows for "adaptive" RT by obtaining an updated MRI scan each day just prior to treatment, adapting the RT plan to take into account any changes in the tumor or the patient's anatomy on that given day. This allows for a smaller (5 mm) margin on the visible tumor as its position can be tracked daily. The goal of this study is to use adaptive RT with small margins to demonstrate that the local control of the visible tumor is not compromised compared to the large volumes used with standard non-adaptive RT, while determining whether smaller margins lead to decreased radiation toxicity and therefore improved quality of life by minimizing radiation exposure.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Glioblastoma Multiforme | Glioblastoma | CURATED_BROADER | 0.80 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Reduced margin adaptive radiotherapy | Radiation | — | UNRESOLVED |
Design
Arms and outcomes
Arms (0)
[]Primary outcomes (1)
- measure
- Imaging-detected tumor recurrence at the edge of the radiation volume ("marginal" failure)
- timeFrame
- Within 1 year from end of radiation
- description
- The presence of tumor on contrast-enhanced MRI between 1-2 cm from the edge of the treated radiation volume (commonly known as a marginal failure) within 1 year from radiation.
Secondary outcomes (5)
- measure
- Tumor volume changes during RT
- timeFrame
- 6 weeks
- description
- Change in gross tumor volume (%) from start to end of RT
- measure
- Acute radiation toxicity based on RTOG/EORTC Common Toxicity Criteria
- timeFrame
- 6 weeks
- description
- Grades 1-4 toxicity during RT in the following categories: skin, CNS, eye, ear, and hematological
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Patients aged 18 years and older * Histopathologically confirmed malignant glioma of the brain, Grade 4 (GBM) * Eligible for RT in 15 or 30 fractions with or without chemotherapy (temozolamide) * Expected survival greater than 12 weeks * WHO performance status less than or equal to 2 * Able to converse and answer questionnaires in English language * Has a maximum final planning volume less than 150 cm3 Exclusion Criteria: * Contraindications to MRI examination as per standard MRI screening policy * Contraindication to Gadolinium-based contrast media * Unable to lie flat in a supine position for 30 minutes * Poor baseline kidney function with an eGFR \< 60 mL/min * Unable to tolerate immobilization in a head thermoplastic mask * Patients \>140 kg and/or a circumference \>60cm * Previous cranial irradiation * Infratentorial tumour extent, multifocal of leptomeningeal disease * Unable to give informed consent
References
Publications (2)
- DERIVEDDetsky JS, Chan AW, Moore-Palhares D, Safavi AH, Perry J, Fat MJL, Atenafu EG, Das S, Lipsman N, Heyn C, Maralani P, Czarnota GJ, Ruschin M, Keller B, Lau A, Chen H, Myrehaug SD, Soliman H, Tseng CL, Sahgal A. MRI-guided adaptive radiotherapy for high grade glioma (UNITED): a single-centre, single-arm, non-inferiority, phase 2 trial. Lancet Oncol. 2026 Jun;27(6):729-737. doi: 10.1016/S1470-2045(26)00088-4. Epub 2026 May 14. PMID 42134380
- DERIVEDLawrence LSP, Chan RW, Chen H, Stewart J, Ruschin M, Theriault A, Myrehaug S, Detsky J, Maralani PJ, Tseng CL, Soliman H, Jane Lim-Fat M, Das S, Stanisz GJ, Sahgal A, Lau AZ. Diffusion-weighted imaging on an MRI-linear accelerator to identify adversely prognostic tumour regions in glioblastoma during chemoradiation. Radiother Oncol. 2023 Nov;188:109873. doi: 10.1016/j.radonc.2023.109873. Epub 2023 Aug 26. PMID 37640160