About this trial
To improve outcomes for childhood cancer patients through the implementation of precision medicine.
Eligibility criteria
Qualifiers
Age < 18 years Note: Individual patients aged 19 - 25 years old with a pediatric cancer, e.g., neuroblastoma, may be enrolled after discussion with, and at the discretion of, the Study Chair or their delegate.
Life expectancy >6 weeks at time of enrolment
Consent i. Signed and dated informed consent for study enrolment from participant aged ≥ 18 years or from parent/guardian of participant aged <18 years. ii. Separate signed and dated informed consent for understanding the role of germline testing and choice for the return of germline results.
Disqualifiers
None
Trial design
Treatments tested in this trial
- Whole Genome Sequencing
- RNA seq
- DNA Methylation
- Targeted Panel Sequencing
- High Throughput Sequencing (in vitro)
- Patient Derived Xenograft (PDX)(in vivo)
- Liquid Biopsy
Treatment groups
13
Treatment groupsSee each treatment group below.
Sponsors and collaborators
Australian & New Zealand Children's Haematology/Oncology Group
Lead sponsor
Children's Cancer Institute (CCI)
Collaborator
Minderoo Foundation
Collaborator
Medical Research Future Fund
Collaborator