CClinicalTrials.gg
CompletedNCT05402241IRD-GBMUpdated May 23, 2024

IRD at Admission Predicts Survival of GBM Patients - a Prospective Pilot Study

An observational study in Glioblastoma Multiforme, sponsored by University of Manitoba. Completed at 2 sites in Canada. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-05-23.

Sponsored by University of Manitoba · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
52
Ages
18 Years and older
Sex
All
01

Study summary

Glioblastomas (GBM) are the most common primary malignant brain tumor with a very high recurrence rate and an average survival of 14 months. Identifying an imaging biomarker to predict recurrence is critical. Using a special MRI technique called diffusion weighted imaging (DWI), a recent retrospective study described isolated restricted diffusion (IRD) foci. The presence of IRD was found in 40% of patients with GBM on index imaging and was associated with longer survival. IRD foci are not currently identified as having a tumor focus and are not included in treatment strategies and guidelines. These findings need to be confirmed in a prospective study. The investigators propose a prospective pilot study to establish the incidence of IRD on the index imaging of patients with GBM. The investigators will collect surgical samples from these foci to establish the histological and molecular signature to confirm GBM in these newly identified foci. The results from this pilot study will guide the planning of a larger well powered multicenter study that will help establish IRD as an imaging biomarker in the GBM management guidelines, which will help improve the outcomes in patients with GBM.

Read the detailed description

Glioblastomas (GBM) are the most common type of primary malignant brain tumor with a very high rate of recurrence. The average survival of patients with GBM is 14 months, and the 5-year survival rate is approximately 4 to 5%. Identifying an imaging biomarker to predict recurrence is critical. Using a special MRI technique called diffusion weighted imaging (DWI), the investigators recently described a focus of isolated restricted diffusion (IRD) in a retrospective study. Presence of IRD was found in 40% of patients with GBM on index imaging and was associated with longer survival. The foci of IRD are not currently identified as having a tumor focus and are not included in treatment strategies and guidelines. The results from this pilot study will help plan for a larger well powered multicenter study that will help establish IRD as an imaging biomarker in the GBM management guidelines. The investigators hypothesize that IRD foci when present, are foci of GBM and when untreated, will be the site of recurrence.

This pilot study will use a prospective cohort study design, to establish the incidence of IRD on the index imaging of participants with GBM. Surgical samples will be collected from these foci to establish the histological and molecular signature to confirm GBM in these newly identified foci. The study population will include patients that present with newly diagnosed with GBM. All newly diagnosed GBM participants will be screened for the study using the study inclusion and exclusion criteria. After the standard of care MRI/DWI is done and reviewed, eligible participants will be approached by the research team, for discussion of the study and potential consent for participation. All participants will undergo further treatment and management as per institutional standard including the clinical and imaging follow up. Each MRI will be screened by experienced neuro-radiologists to identify the presence of isolated restricted diffusion foci. In those participants with isolated restricted diffusion foci on MRI, the neurosurgeon (on for the day) will assess the feasibility and safety of targeted biopsy from this focus. The targeted biopsy will only be considered when it is deemed safe and feasible based on the location and surgical approach, which will be determined by the neurosurgeon. This will reduce any undue risk for research purposes. The biopsy samples will undergo standard of care laboratory histopathological and molecular testing to establish the pathological and molecular signatures of these tumors. The neuropathologic examination will be performed by neuropathologists. Informed consent will be obtained from the patients to participate in the study.

The aim of this study is to establish a new imaging biomarker and to determine its association with known molecular alterations in GBM. The investigators will also explore the incidence of isolated restricted diffusion in GBM participants, the number of IRD foci that proceed to contrast enhancement on follow up, the true number of IRD foci, and the survival pattern of the study participants with isolated restricted diffusion.

02

Conditions studied

  • Glioblastoma Multiforme

Browse trials for

Keywords

  • Glioblastoma, Multiforme
  • Isolated Restricted Diffusion foci
03

In context

Glioblastoma

1,920 studies on the registry are indexed under Glioblastoma; 450 are open to participants now.

This study's enrollment of 52 is below the median of 60 across 188 observational studies indexed under Glioblastoma.

Browse Glioblastoma studies →

Lead sponsor

University of Manitoba is the lead sponsor of 542 studies on the registry; 87 are open to participants now.

Of its 12 completed or terminated interventional studies of FDA-regulated products, 5 (42%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

newly diagnosed patients with GBM

Inclusion criteria

  • At least 18 years old
  • Patients with suspected GBM on initial MRI of brain
  • MRI scans with isolated restricted diffusion foci noted

Exclusion criteria

Exclusion Criteria:

  • Participants who are pregnant
  • Known contraindication to MRI contrast agent, e.g., allergy or anaphylactic reaction
  • Known end-stage renal disease
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
52 participants (actual)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Incidence of isolated restricted diffusion (IRD) in GBM patients

    proportion of GBM participants with IRD

    Time frame: Upon completion of the study, which will be approximately 2 years

  2. Incidence of IRD foci proceeding to contrast enhancement on 3 month follow up

    proportion of participants that have contrast enhancement on 3 month follow-up

    Time frame: through completion of the study approximately 2 years

  3. Incidence of IRD foci proceeding to contrast enhancement on 6 month follow up

    proportion of participants that have contrast enhancement on 6 month on follow-up

    Time frame: through completion of the study approximately 2 years

  4. Incidence of IRD foci that are from the GMB foci

    proportion of IRD foci that originate from the GBM foci

    Time frame: through completion of the study, approximately 2 years

  5. relationship of molecular alteration with GBM foci and the IRD

    descriptive analysis

    Time frame: Upon completion of the study approximately 2 years

  6. Survival patterns of GBM participants with IRD

    mortality

    Time frame: Upon completion of the study approximately 2 years

07

Study locations

2 sites
  • Health Sciences Centre
    Winnipeg MB, Manitoba R3A 1R9, Canada
  • University of Manitoba
    Winnipeg, Manitoba R3E 3P5, Canada
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 23, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05402241
Lead sponsor
University of Manitoba
Collaborators
CancerCare Manitoba
Responsible party
Sponsor
First posted
Jun 2, 2022
Start date
Oct 21, 2021
Primary completion
Nov 15, 2023
Completion
Nov 15, 2023
Last update
May 23, 2024

Study contacts

Jai Shankar, MD
principal investigator · University of Manitoba

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2024. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion