Cancer Council Queensland shared on LinkedIn:
“Did you know…?
One of the world’s very few databases dedicated to recording childhood cancer is managed right here, at CCQ, Viertel Cancer Research Centre?
The Australian Childhood Cancer Registry contains 26,350 records of every child diagnosed with cancer in Australia since 1983.
Each year, about 900 children aged 0-14 will be diagnosed with cancer and our researchers collect and manage their clinical and treatment information for the Registry.
These data pave the way for more research and new studies that are essential for improving outcomes for children affected by cancer.
September is the global Childhood Cancer Awareness Month, organised by Childhood Cancer International and International Society of Paediatric Oncology – SIOP.
While childhood cancer is rare – making up only about 1% of all cancers – its numbers are gradually increasing.
Our research into childhood cancers, including our management of the Australian Childhood Cancer Registry, is focused on understanding why, improving survival rates, tailoring services and offering the support young people and their families need.”
Natalie Bradford, Professor in Childhood Cancer and Palliative Care, Director of Paediatric Palliative Care Centre of Research Excellence, added on LinkedIn:
“I am super proud to be leading the Childhood Cancer Research Group at CCQ, Viertel Cancer Research Centre, progressing this important work with our fabulous team, including Peter Baade, Louise Marquart, Charly McIntyre, James Retell, Leisa O’Neill, Sheree Rye and supported by our Advisory Group, including Kate Cantrell.
This Gold September is a time to raise awareness of childhood cancer and the need to cure more and care for all.”
You can also read: Children with cancer do not need sympathy. They need systems that work – Gevorg Tamamyan
