Ultra-low-input cell-free DNA sequencing for tumor detection and characterization in a real-world pediatric brain tumor cohort
Molecular profiling of pediatric central nervous system (CNS) tumors has important clinical utility for guiding diagnostic and therapeutic strategies. Cell-free DNA (cfDNA) from liquid biopsies has been used for minimally invasive tumor profiling and longitudinal disease assessment in adult oncology and pediatric hematology. However, in pediatric neuro-oncology, low cfDNA yields pose a major barrier to translating these assays from bench to bedside. Here, we implemented a low-coverage whole genome sequencing (lcWGS) assay for picogram-level cfDNA inputs and applied it to liquid biopsies from a sizeable, population-based, cross-entity pediatric CNS tumor cohort (n = 56 patients). Applying this protocol, cfDNA whole genome profiles were successfully acquired from all liquid biopsy samples (n = 61/61 serum, n = 56/56 CSF, 100%). Based on copy number variations (CNVs), circulating-tumor DNA (ctDNA) was detected in 2/61 serum (3%) and in 25/56 CSF (45%) samples across various brain tumor entities. The integration of cfDNA results with clinical data demonstrated the utility of CSF lcWGS as a biomarker assay at diagnosis to distinguish cancerous from non-cancerous pineal region lesions (n = 6 patients). Additionally, serial CSF assessment in n = 9 patients (n = 29 CSF samples) enabled minimally invasive disease monitoring, with the added value of molecular profile availability in n = 4/6 (67%) patients at relapse. Proof-of-concept data show the feasibility of serial CSF lcWGS to reveal tumor evolution, tumor heterogeneity and potential therapeutic vulnerabilities in a case of medulloblastoma and germ cell tumor. Our study underscores the clinical utility of a robust lcWGS-based liquid biopsy assay optimized for low-input samples. We identify use-cases for implementing liquid biopsies in the clinical management of pediatric CNS tumor patients and provide a strong rationale for integration into future trials.
Authors
- Kristiina Nordfors (ORCID: https://orcid.org/0000-0002-3680-4524)
- Ahmed El Damaty (ORCID: https://orcid.org/0000-0003-0146-8943)
- Olli Lohi (ORCID: https://orcid.org/0000-0001-9195-0797)
- Kristian W. Pajtler (ORCID: https://orcid.org/0000-0002-3562-6121)
- Fabian Rosing (ORCID: https://orcid.org/0000-0003-4749-2666)
- Florian Iser (ORCID: https://orcid.org/0009-0003-6514-817X)
- Markus Mieskolainen
- Stefan M. Pfister (ORCID: https://orcid.org/0000-0002-5447-5322)
- Tom T. Fischer (ORCID: https://orcid.org/0000-0002-2138-9102)
- Agnes M E Finster
- Tatjana Wedig
- Benedikt Brors (ORCID: https://orcid.org/0000-0001-5940-3101)
- Felix Sahm (ORCID: https://orcid.org/0000-0001-5441-1962)
- Paulina Schad (ORCID: https://orcid.org/0009-0007-0952-8396)
- Nathalie Schwarz
- Joonas Haapasalo (ORCID: https://orcid.org/0000-0002-6468-4937)
- Kendra K. Maaß (ORCID: https://orcid.org/0000-0001-9357-5038)
- Pitithat Puranachot (ORCID: https://orcid.org/0000-0002-6786-9240)
- Martin Sill (ORCID: https://orcid.org/0000-0001-7616-7665)
- Jochen Meyer (ORCID: https://orcid.org/0009-0000-8610-0077)
- Hannu Haapasalo (ORCID: https://orcid.org/0000-0003-4389-7391)
- Stefanie Volz
Institutions
- Tampere University (FI)
- German Cancer Research Center (DE)
- Heidelberg University (DE)
- University Hospital Heidelberg (DE)
- Chulabhorn Hospital (TH)
- National Center for Tumor Diseases (DE)
- Hopp Children's Cancer Center Heidelberg (DE)
- Tampere University Hospital (FI)
- Tampere University (FI)
- Fimlab (Finland) (FI)
- Heidelberg University (US)
Publication Details
- Journal
- Acta Neuropathologica Communications
- Published
- 2025-06-28
- DOI
- https://doi.org/10.1186/s40478-025-02024-w
- Citations
- 6
- Primary Topic
- Cancer Genomics and Diagnostics
- Type
- article
- Field-Weighted Citation Impact
- 5.62
Funders
- Deutsches Krebsforschungszentrum
- Bundesministerium für Bildung und Forschung
- Bundesministerium für Gesundheit
- Deutsche Krebshilfe
- Deutsche Kinderkrebsstiftung
- Tays
- Deutschen Konsortium für Translationale Krebsforschung