There are so many ways you can help make a difference in the lives of patients and families today.
Our 2020 Research Symposium is set for Saturday, May, featuring a full slate of speakers who will explore various aspects of research in finding a cause and a cure for brain tumours.
Dr. Emily Walker – Brain Tumour Registry of Canada
Dr. John Kelly – Glioblastoma Initiating Stem Cells
Lori Boomer – Taite Boomer Foundation
Dr. Aru Narendran – Pediatric Cancer Vaccines
Dr. Michael Blough – Initiation and Progression of Glioblastoma
There is no cost to the event, which is open to the public. Anyone affected by a brain tumour who has an interest in learning more about research is welcome. Because this is an online symposium, spaces are limited. Please sign up early to reserve your spot. Register online here.
37 years ago, Pam and Rolando Del Maestro co-founded Brain Tumour Foundation of Canada and over the years have fostered students in the field of brain tumour research by providing them with varied opportunities to present their ideas and engage with physicians and researchers in the field of neuro-oncology and neuroscience.
Brain Tumour Foundation of Canada thanks our co-founders Pam and Rolando Del Maestro for establishing this visionary opportunity.
Since the awards were established in 2017, seven teams have been awarded monetary prizes ranging between $500-$1,000. Congratulations to the recipients.
In 2019 we expanded the Research Grant program to include feature grants.
Grants of up to $50,000 will be available for research taking place within Canada to improve the quality of life for patients, survivors and caregivers across Canada affected by a brain tumour.
In 2019 the Feature Grant was focused on improving quality of life for patients, survivors and caregivers across Canada affected by a brain tumour.
In 2020 we shifted focus to pediatric brain tumours, providing hope and action for our most vulnerable population.
Kids need to do more than survive brain cancer. They deserve to thrive. That’s the aim of the most significant research grant in our history, made possible thanks to the generosity of donors.
Medulloblastoma is the most common childhood brain cancer. Because of kids’ growing brains and bodies, chemotherapy and radiation are detrimental to their ongoing development. Those who do survive a brain cancer diagnosis are often left with devastating side effects that change their lives forever. Children treated with chemotherapy or radiation are eight times more likely to develop severe health problems, especially as they age into their 20s and 30s. The higher the dose of drugs and the more extensive the radiation, the more problems are to emerge. The impact of brain cancer treatments can include: blindness, fertility issues, hearing loss, learning and emotional disabilities, memory deficits, stunted puberty or hormone problems, the list goes on.
Thanks to a brain tumour research grant funded in 2014, renowned researcher, Dr. Michael Taylor, was the first to discover that medulloblastoma wasn’t just one form of brain cancer, but four distinct types — each with their own DNA footprint, and therefore potential treatment needs.
Now Dr. Taylor and his team of researchers want to know how each type of medulloblastoma changes in response to treatment, and how to develop personalized care for every child diagnosed. This means the most aggressive treatments are only used on the most aggressive brain cancers, saving children from life-changing side effects or secondary diseases.
Dr. Taylor and his team have now completed the first year of this five–year research project. Thanks to the first year of research, we now know that there are at least ten different sub-types of medulloblastoma, with a much higher degree of differences between tumours than first identified.
By identifying the precise degrees of difference between medulloblastoma types, Dr. Taylor and his team aim to classify these differences, so treatment is focused specifically to a patient’s needs. Dr. Taylor’s completed research will provide better, less toxic treatments to patients with lower-risk medulloblastoma.
Dr Taylor and his team have now identified 12 subtypes of medulloblastoma. They have also discovered that each subtype is completely different at the time of recurrence, so another resection is needed to determine the new type. This also means that a new treatment might be necessary for the new subtype. Dr Taylor and his team continue to work on what those treatment types should be. More to come…
In 2018, Dr. Taylor and his team published a breakthrough study that showed, for the first time, that medulloblastoma can also spread through the blood. Most deaths associated with medulloblastoma are caused by metastatic disease, where the tumour has spread to a new site in the brain. For decades, researchers believed that medulloblastoma spread through the cerebrospinal fluid. This surprising discovery completely changes our understanding of how medulloblastoma spreads and opens up new avenues for diagnosis and treatment.
Thanks to the generosity of donors, as well a partnership with the Canadian Cancer Society and matching funds from Brain Canada, the fundraising goal of $1.25 million dollars has been reached, meaning that this project will be fully funded. While the funding for this project is now complete, the research continues. We look forward to updating you all on the work that Dr. Taylor is doing and the impact that this is having for patients!
Research on brain tumours depends on the availability of human brain tissues. Although other research models have been developed, none completely reproduce the pathophysiology of human brain tumours. This is why Brain Tumour Foundation of Canada funds the Brain Tumour Tissue Bank. This ‘bank’ provides the raw materials essential for basic brain tumour research.
The Brain Tumour Tissue Bank collects, processes and catalogues brain tumour tissue samples and ships them across Canada and around the world. Over 1,000 cases have been catalogued since the tissue bank opened in 1991, resulting in a library of several thousand frozen brain tumor specimens, which are available to researchers upon request.
“The BTTB is an outstanding and necessary resource for the Canadian Brain Tumour Community. It is only with ongoing support from the BTFC that it will continue to flourish. I will continue to use and support the BTTB on a cost recovery basis and recommend the tumour bank to other Canadian neuro-oncology researchers, especially those with few if any local options to procure brain tumour tissues.”
Dr. David Eisenstat, MD, MA, FRCPC Director of Neuro-Oncology: Adult and Pediatric; CancerCare Manitoba,; Winnipeg, MB. Dr. Eisenstat is a member of the Professional Advisory Group for Brain Tumour Foundation of Canada.
For more information about current samples or for a quick search about what is available, please contact Marcela White at firstname.lastname@example.org.
This short video shows the Brain Tumour Tissue Bank and explains the process of collecting and processing the tissue that is so critical for research.
Brain Tumour Foundation of Canada partners with the Brain Tumor Funders’ Collaborative to extend the impact of research dollars.
Five North American funding organizations make up the Brain Tumor Funders’ Collaborative. The organization includes Brain Tumour Foundation of Canada along with five other non-profit, philanthropic and advocacy organizations from the United States. By working together we can accelerate progress in brain tumor research. The groups have worked together to fund two previous initiatives (details below) and are now exploring a third joint project. When this is finalized, the projects details, and any applicable calls for applications will be posted here.
The members of the Brain Tumour Funders’ Collaborative are:
In January 2019 the BTFC announced $3 million in grants to four multi-institutional teams of researchers and clinicians studying immunotherapy in primary brain tumours. Read the Press Release here.
The four funded projects will examine vaccination strategies, the tumour’s micro-environment, anti-tumour T-cells, and personalized immunotherapy approaches. They were selected during a multi-stage review process from more than 79 responses to the BTFC call for proposals.
The following institutions will be receiving $750,000 BTFC grants over the next three years:
Active vaccination and the timing of checkpoint blockade dictate effective immunotherapy for glioblastoma
David Geffen School of Medicine at UCLA
Project Manager: Robert Prins
Harnessing the brain tumour immune-microenvironment to enhance therapeutic efficacy
Project Manager: Daniela Quail
Interrogating anti-tumor T-cells To develop adoptive cell transfer (ACT) Immunotherapy for pediatric high-grade gliomas
UPMC Children’s Hospital of Pittsburgh
Project Manager: Gary Kohanbash
Three dimensional immuno-genomics approach to personalized neoantigen-based immunotherapy
University of California, San Francisco
Project Manager: Joseph Costello