Abstracts/Presentation Description
Vanessa Tyrrell1;2, Chelsea Mayoh2;3, Paul Ekert2;3;4, Mark Cowley2;3, David Ziegler2;3;5, Marie Wong2;3, Paulette Barahona2, Mark Pinese2;3, Michelle Haber2;3, Rob Salomon2, Eliza Courtney2;5, Richard Lock2;3, Noemi Fuentes-Bolanos2;3;5, Glenn Marshall2;3;5, Meera Warby5, Toby Trahair2;3;5, Dong Anh Khuong Quang6;7, Claire Wakefield3, Katherine Tucker3;5;8, Kristine Barlow-Stewart2;9, Bhavna Padhye10, Loretta Lau2;3;5
1UNSW Sydney, School of Clinical Medicine, UNSW Medicine and Health, Sydney, Australia; 2Children’s Cancer Institute, Randwick, Australia; 3UNSW Sydney, School of Clinical Medicine, UNSW Medicine & Health, Sydney, Australia; 4Peter MacCallum Cancer Centre, Melbourne, Australia; 5Sydney Children’s Hospital, Randwick, Kids Cancer Centre, Randwick, Australia; 6The Royal Children’s Hospital Melbourne, Children’s Cancer Centre, Parkville, Australia; 7Murdoch Children’s Research Institute, Parkville, Australia; 8Prince Of Wales Hospital, Hereditary Cancer Clinic, Randwick, Australia; 9University of Sydney School of Medicine, Camperdown, Australia; 10The Children’s Hospital at Westmead, Cancer Centre for Children, Westmead, Australia
Precision medicine is revolutionising the way cancers are detected, characterised, and treated, by identifying targetable vulnerabilities by matching genomic profiling with molecularly targeted agents. The Zero Childhood Cancer (ZERO) national precision medicine program was launched, initially for children with the most aggressive cancers with a less than 30% chance of survival. ZERO utilises comprehensive molecular profiling, integrating germline and tumour whole genome sequencing, RNA sequencing and methylation profiling, and where possible, in vitro and in vivo testing of patient tumour cells for response to chemotherapeutic and novel targeted agents.
Between September 2017 and October 2023, 1000 children with high risk, rare, and undiagnosable cancers were enrolled on ZERO’s first national trial. Recent analyses of 384 consecutively enrolled high-risk child cancer patients, with >18 months of follow up, demonstrated that those receiving a precision-guided treatment (PGT), informed by comprehensive multiomic profiling, led to doubling (27% vs 11%) 2 year progression free survival when compared to standard-of-care cytotoxic therapies and a substantive 5 times higher when comparing PGT to that of an unguided novel therapy (a novel agent not chosen on the basis of molecular findings).
These findings demonstrate the power of multiomic profiling to improve outcomes for children with high-risk cancer. In November 2023, ZERO became available to all Australian children and young people diagnosed with cancer, irrespective of cancer type, stage, or risk, with over 1000 children enrolled in the first 12 months. ZERO is changing the model of care for Australian children with cancer, with the goal of guiding more effective treatment options and improving long-term outcomes for all children with cancer.