This media release was provided by Count Me In.
Count Me In, a non-profit research initiative, has launched the Brain Cancer Project, a patient-partnered effort that enables anyone in the USA and Canada who has ever been diagnosed with a primary brain cancer to collaborate in a research project aimed at accelerating discoveries for this disease.
The Brain Cancer Project will partner with patients through social media and advocacy groups in order to generate data that represents the spectrum of people affected by this disease. While the project is open to patients who are 18 or older, it will expand to include paediatric patients in the future. All data will be freely available to the global biomedical community.
In the United States, approximately 17,000 people die from brain cancer every year, making this one of the top 10 causes of cancer deaths in the United States, according to statistics from the National Cancer Institute. Approximately 166,000 people are living with brain cancer in the US, and more than 23,000 were newly diagnosed in 2018. Both diagnosis and survival rates for brain cancer vary a great deal among patients, and researchers still do not fully understand why.
Minderoo Foundation, a philanthropic organisation based in Perth, Australia and established by Andrew Forrest AO and Nicola Forrest AO, is a key partner in this new project. Their generous financial support to this project underscores Minderoo Foundation’s commitment to increasing the availability of patient data and accelerating cancer research.
“Minderoo Foundation is incredibly excited about the potential of this new collaboration with
Count Me In,” Mr. Forrest said.
“Brain cancer remains a frightening diagnosis that we know far too little about. This collaboration will help expand CMI’s efforts in patient-partnered cancer research and, importantly, launch critical laboratory work to map the genetic vulnerabilities of various brain cancers. This new paradigm has the potential to unlock understanding, spark new, collaborative strategies for treatment and empower thousands of people to join this patient-led research revolution.”
“We want to do everything humanly possible to develop better treatments for people with brain
cancer. Through this initiative, we will extend our understanding of the molecular changes that
occur throughout the spectrum of brain cancers,” said Patrick Wen, MD, Director of the Center For Neuro-Oncology at Dana-Farber Cancer Institute and Professor of Neurology at Harvard Medical School.
Patients diagnosed with a primary brain cancer, such as glioblastoma, astrocytoma, or oligodendroglioma, can join the project. To participate, patients first fill out a survey covering demographic information and cancer history as well as a research consent form.
Afterwards, they receive a kit in the mail for collecting a saliva sample so that researchers can compare the patient’s genetic information with tumor DNA. Some participants may receive a blood collection kit as well.
The project will generate anonymised genomic, clinical, and patient-reported data that will be shared as a comprehensive dataset with the entire research community in order to accelerate the development of future therapies. The data will be made available to enable researchers globally via scientific web portals to access and learn from it, so as to fuel their research programs and accelerate discoveries in cancer research. The team will release new batches of data on a regular basis.
The Brain Cancer Project was built with an advisory council comprised of patients and caregivers and builds on the infrastructure, processes, successes, and lessons learned from four other patient-partnered cancer research projects launched by Count Me In: the Metastatic Breast Cancer Project, the Angiosarcoma Project, the Metastatic Prostate Cancer Project, and the Esophageal and Stomach Cancer Project, which combined have almost 7,000 registered patients.
In addition, input was gathered from scientists, clinicians, and advocacy partners to ensure that the project encompasses a wide variety of the brain cancer community. The project is proud to have the American Brain Tumor Association, the National Brain Tumor Society, Accelerate Brain Cancer Cure, and Oligo Nation as advocacy partners. All Count Me In projects share a core commitment of partnering closely with patients to speed both drug discovery and biological understanding of cancer.
“Brain cancer is an insidious threat: the nature of the disease infiltrates areas of the brain responsible for language, memory, personality, motor function, and more. In short, brain cancer threatens to rob patients of who they are. The Count Me In Brain Cancer Project equips patients with an avenue to proactively face this disease by locking arms with researchers and taking action in a meaningful way. On a community level, the Count Me In Brain Cancer project promises to reveal new insights about this devastating disease; on a personal level, Count Me In recognizes the value of individual patients standing up and taking action. Few things are more rewarding than recognising the value of individuals to move mountains though partnership,” said Adam Hayden, Project Advisory Council member.
“As with our previous projects, patients and advocates have had an important voice in every
aspect of the BCProject’s development and design,” said Corrie Painter, Broad Institute Associate Director of Operations and Scientific Outreach, who plays key roles in all CMI projects.
“Their perspectives and advice have been immensely valuable in teaching us how best
to approach and partner with patients with this disease, and making sure that our efforts
Established by Andrew and Nicola Forrest in 2001, we are a modern philanthropic organisation seeking to break down barriers, innovate and drive positive, lasting change. Minderoo Foundation is proudly Australian, with eight key initiatives spanning from ocean research and ending slavery, to collaboration in cancer and community projects.