Core focus across ChiLTERN (liver tumors), ITCC-P4 (preclinical platform), CLOSER (childhood leukemia), VAGABOND (paediatric cancers), TREL, and PanCareSurPass (survivorship).
ST ANNA KINDERKREBSFORSCHUNG VEREIN
Vienna-based pediatric cancer research institute specializing in preclinical oncology models, genomic diagnostics, and precision medicine for childhood cancers.
Their core work
St. Anna Children's Cancer Research Institute (CCRI) in Vienna is a dedicated pediatric cancer research center focused on improving diagnosis, treatment, and survival outcomes for children with cancer and rare diseases. They specialize in preclinical drug development, genomic profiling (NGS workflows), and translational research that bridges laboratory discoveries to clinical application in childhood leukemia, neuroblastoma, and solid tumors. Their work spans from molecular-level investigations — functional genomics, biomarker discovery, pharmacogenetics — to large-scale European efforts in standardizing precision medicine for pediatric oncology.
What they specialise in
ITCC-P4 built POC platforms using PDX, GEMM, and organoid models; VAGABOND validated target-drug combinations; PRIMAGE developed imaging biomarkers.
Instand-NGS4P focused on standardized NGS workflows for personalized therapy; FIND-seq interrogates non-coding DNA in leukemia; VAGABOND validates actionable genomic aberrations.
EJP RD (European Joint Programme on Rare Diseases), iDysChart (immune dysregulation charting), and ERICA (rare disease research coordination).
PRIMAGE developed predictive in-silico analytics for neuroblastoma/DIPG; PanCareSurPass implements digital Survivorship Passports with EHR interoperability.
How they've shifted over time
In the earlier period (2016–2019), St. Anna focused heavily on disease-specific preclinical research — building tumor models (PDX, organoids), studying neuroblastoma and DIPG through imaging biomarkers, and establishing pediatric cancer research networks. From 2020 onward, the focus shifted markedly toward genomic standardization, NGS workflow integration, pharmacogenetics, and digital infrastructure (e-reporting, e-medication, survivorship passports). This evolution reflects a move from discovery-stage research toward clinical implementation and diagnostic standardization.
St. Anna is moving from laboratory-based cancer biology toward standardized, digitally-integrated precision medicine pipelines ready for clinical deployment in pediatric oncology.
How they like to work
St. Anna operates exclusively as a consortium participant — across all 12 H2020 projects, they never served as coordinator. They consistently join large European consortia, having worked with 248 unique partners across 38 countries, indicating they are a valued specialist contributor rather than a project driver. This makes them a reliable, low-friction partner for coordinators seeking deep pediatric oncology expertise without competition for leadership roles.
With 248 unique consortium partners spanning 38 countries, St. Anna has one of the broadest collaboration networks in European pediatric cancer research. Their reach extends well beyond Europe — the CLOSER project explicitly bridges South America and Europe — though the core network centers on EU member states.
What sets them apart
St. Anna is one of very few research centers in Europe exclusively dedicated to childhood cancer, giving them unmatched depth in pediatric oncology that generalist cancer institutes cannot replicate. Their combination of preclinical model expertise (organoids, PDX, GEMM) with genomic diagnostics capability (NGS, pharmacogenetics, bioinformatics) makes them a one-stop partner for translating pediatric cancer research into clinical-grade tools. For consortium builders, they bring both the disease-specific knowledge and the technical infrastructure needed for precision medicine projects targeting childhood cancers.
Highlights from their portfolio
- ITCC-P4Largest funded project (EUR 102,811) building a comprehensive pediatric preclinical POC platform using PDX, GEMM, organoid, and biomarker approaches across solid and brain tumors.
- EJP RDMassive European Joint Programme on Rare Diseases connecting rare disease data, omics, FAIR principles, and patient empowerment — positions St. Anna at the intersection of pediatric cancer and rare disease policy.
- Instand-NGS4PRepresents St. Anna's strategic pivot into standardized NGS diagnostics, covering the full pipeline from preanalytics to bioinformatics under IVDR compliance for both pediatric and adult cancers.