80% of childhood cancer survivors experience long-term effects from their treatment.

More children and adolescents are surviving cancer than ever before. This is a major health success. But for many survivors and families, cancer and its treatment can have lifelong health, emotional, social and practical impacts.
Australia has dedicated clinicians, services, researchers and community organisations working to support survivors. The challenge now is to connect that expertise, strengthen the evidence, and turn what we learn into care thatis consistent, equitable and sustainable.
Diagnosed with cancer in Australia every year
Under age 50 lives with a history of cancer diagnosed during childhood
Experience at least one long-term health problem
Report financial strain from direct medical expenses
Experience significant employment disruptions
As adults, are not in paid employment, globally
Survivorship begins at diagnosis and continues through every stage of life.
Some survivors may need lifelong monitoring for late effects of cancer or treatment. Others may need support to navigate transitions between paediatric and adult health services, manage emotional wellbeing, continue education or work, or coordinate care across multiple providers.
No two experiences are the same. That is why survivorship care must be informed by a survivor’s diagnosis, treatment history, individual risks and changing needs over time.
Important survivorship work is already happening in hospitals, health services, research institutions and community organisations across Australia. However, the available support is not consistent across locations, services or life stages.
Australia does not yet have a comprehensive national approach to support lifelong, risk-based follow-up for childhood and adolescent cancer survivors.
International guidance helps clinicians understand potential health risks after cancer treatment. But it does not, by itself, an important question - which models of care work best for different survivors and families in Australia?
A coordinated research agenda can help Australia move from fragmented pathways to evidence-informed survivorship care that is fairer, more connected and built to last.
Research that:
• Develops and strengthens national best-practice approaches to survivorship and supportive care for children, adolescents and young adults with cancer.
• Tests and implements early interventions, digital tools and new approaches that improve long-term quality of life and the experience of survivors and families.
• Builds the evidence needed to guide policy, service planning and practical improvements across the health system.
Children’s Cancer CoLab is working with survivors, families, clinicians, researchers and sector partners to strengthen childhood and adolescent cancer survivorship research in Australia.
Our focus is on generating practical evidence that can improve lifelong follow-up, supportive care and quality of life.
This work builds on CoLab’s existing survivorship initiatives, including survivor and family consultation, the Survivorship Reference Group, the National Landscape and Economic Assessment, and Cancer Australia’s development of the first national Optimal Care Pathway for Children with Cancer.
A united sector call for survivorship to be a core part of every cancer care plan, roadmap and research agenda

We welcome applications from researchers and clinicians whose work aligns with our current priorities. All proposals are reviewed for scientific merit, clinical impact, strategic alignment, and real-world impact on patients, survivors, and families.