Actively Recruiting

Age: 18Years +
All Genders
NCT05326334

THERApeutic Outcomes Related to Gut microBIOME in Glioblastoma (GBM) Patients Receiving Chemo-radiation (THERABIOME-GBM)

Led by Ottawa Hospital Research Institute · Updated on 2023-04-18

20

Participants Needed

1

Research Sites

339 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This is a pilot or feasibility study to test the study plan and to find out whether enough participants will join a larger study and accept the study procedures. Eligible participants (adults with newly diagnosed glioblastoma multiforme \[GBM\] and had a good tumour resection \[\>= 70% of initial tumour volume\] and plan to receive 6 weeks of chemoradiation followed by up to 6 months of chemotherapy) are asked to donate their own stool samples at 4 different time points during their treatment course. Participants will also complete a 7-day diet diary and two questionnaires about their health-related quality of life. Glioblastoma multiforme (GBM) is the most common and aggressive form of primary brain cancer in adults. The current best evidence-proven treatment for GBM includes maximum safe tumour resection, brain radiation over a 6-week period given with chemotherapy pills called temozolomide (Brand name: Temodal or Temodar), followed by approximately 6 months / cycles of temozolomide. Despite these treatments, the average life expectancy is generally less than 2 years. Researchers are recognizing that the immune system has an important role in directing the effectiveness of chemotherapy, radiation, and newer therapies such as immunotherapies. Some immunotherapies have been quite successful in improving cancer control and survival in other cancers like melanoma (an aggressive skin cancer), but when these drugs were given to patients with GBM, there appeared to only be a small effect. Therefore, finding ways to make existing and new treatments work better should be a priority. Recent scientific studies have shown that the bacteria that make up our stool, often referred to as the gut microbiome, play a major role in regulating the immune system. For example, researchers were able to make patients with melanoma who previously did not respond to immunotherapy become responsive to the treatment after receiving a stool transplant from responders to immunotherapy. This provides proof of concept that we could modify the body's immune environment to favour cancer killing by changing a person's gut bacteria environment. The role of the gut bacteria in patients with brain cancer is poorly understood as very few studies have been published about it in this population. We believe that understanding the composition of the gut microbiome and how it relates to the effectiveness and side effects of treatments in GBM patients will be an important first step to understanding how we can modify the gut microbiome to improve outcomes for patients living with GBM.

CONDITIONS

Official Title

THERApeutic Outcomes Related to Gut microBIOME in Glioblastoma (GBM) Patients Receiving Chemo-radiation (THERABIOME-GBM)

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with newly diagnosed WHO grade 4 glioblastoma, IDH-1 R132H wild type
  • Maximum safe resection (≥70% of initial tumor volume resected)
  • Age 18 years or older
  • Eastern Cooperative Oncology Group (ECOG) performance status 0 to 1, or ECOG 2 if on ≤8 mg/day dexamethasone (or equivalent)
  • Plan to receive 60 Gy radiation with temozolomide within 12 weeks of surgery
  • Patient or substitute decision maker able to provide written informed consent
Not Eligible

You will not qualify if you...

  • Having metastatic or secondary cancer that could affect study outcomes
  • Receiving additional systemic therapies or clinical interventions for glioblastoma other than temozolomide and radiation as described
  • Inability to provide stool samples for the study
  • Any medical or psychological condition that prevents participation as judged by the investigator
  • Patients on new standard care treatments can be included only at investigator discretion if also enrolled in control arm of therapeutic studies

AI-Screening

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Trial Site Locations

Total: 1 location

1

The Ottawa Hospital Cancer Centre

Ottawa, Ontario, Canada, K1H 8L6

Actively Recruiting

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Research Team

T

Terry L. Ng, MD

CONTACT

V

Vimoj Nair, MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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