Building a Pediatric CNS Tumor Liquid Biopsy Program: Overcoming Barriers to Expand Access and Collaboration

Abstract Background Circulating tumor DNA (ctDNA) analysis has emerged as a promising tool for the management of pediatric central nervous system (CNS) tumors. However, implementation remains concentrated to a relatively limited number of specialized centers with established clinical research infrastructure and sequencing expertise. Many pediatric neuro-oncology programs face substantial barriers to developing similar capabilities, limiting broader participation in and contribution to liquid biopsy research. Methods We describe the development of a pediatric CNS ctDNA program at a quaternary children's hospital with limited research infrastructure and genomic testing capabilities. Key elements include protocol development, Institutional Review Board approval, patient identification and enrollment, longitudinal blood and cerebrospinal fluid (CSF) collection workflows, specimen processing and storage procedures, and partnerships for molecular sequencing and analysis. Results Fifty-seven patients were enrolled over four years, resulting in collection of 417 longitudinal blood and cerebrospinal fluid samples. Standardized workflows for enrollment, specimen collection, processing, storage, and clinical annotation were successfully implemented. Strategic funding facilitated stability of a sample biorepository. Successful implementation required coordination among a multidisciplinary team spanning clinical care, research operations, laboratory sciences, and institutional administration. Conclusions Development of a pediatric CNS tumor liquid biopsy program is feasible at institutions without extensive pre-existing liquid biopsy infrastructure. Structural, operational and cultural barriers can be overcome by establishing standardized collection workflows, multidisciplinary collaboration, and external partnerships. Our experience provides a practical framework for other centers seeking to participate in pediatric CNS tumor liquid biopsy research.

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Publication Details

Journal
Neuro-Oncology Pediatrics
Published
2026-10-16
DOI
https://doi.org/10.1093/neuped/wuag056
Primary Topic
Cancer Genomics and Diagnostics
Type
article
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article

Building a Pediatric CNS Tumor Liquid Biopsy Program: Overcoming Barriers to Expand Access and Collaboration

Sharvari Mankame, Floris P Barthel, Jason Scott Hauptman, Kazuhiro Sabet et al.
Neuro-Oncology Pediatrics
Cancer Genomics and Diagnostics
article

Building a Pediatric CNS Tumor Liquid Biopsy Program: Overcoming Barriers to Expand Access and Collaboration

Sharvari Mankame, Floris P Barthel, Jason Scott Hauptman, Kazuhiro Sabet, Benjamin Posorske, David F. Carpentieri, Michael E. Berens, Ross Mangum, Peter A. Chiarelli, Lisa Keller, Shea Gallus, Mario Dias Abrantes, Samantha Bouchal Shockness, Roxanne Sandoval, Edrick Villalobos, Tina Xue
article en

Abstract

Abstract Background Circulating tumor DNA (ctDNA) analysis has emerged as a promising tool for the management of pediatric central nervous system (CNS) tumors. However, implementation remains concentrated to a relatively limited number of specialized centers with established clinical research infrastructure and sequencing expertise. Many pediatric neuro-oncology programs face substantial barriers to developing similar capabilities, limiting broader participation in and contribution to liquid biopsy research. Methods We describe the development of a pediatric CNS ctDNA program at a quaternary children's hospital with limited research infrastructure and genomic testing capabilities. Key elements include protocol development, Institutional Review Board approval, patient identification and enrollment, longitudinal blood and cerebrospinal fluid (CSF) collection workflows, specimen processing and storage procedures, and partnerships for molecular sequencing and analysis. Results Fifty-seven patients were enrolled over four years, resulting in collection of 417 longitudinal blood and cerebrospinal fluid samples. Standardized workflows for enrollment, specimen collection, processing, storage, and clinical annotation were successfully implemented. Strategic funding facilitated stability of a sample biorepository. Successful implementation required coordination among a multidisciplinary team spanning clinical care, research operations, laboratory sciences, and institutional administration. Conclusions Development of a pediatric CNS tumor liquid biopsy program is feasible at institutions without extensive pre-existing liquid biopsy infrastructure. Structural, operational and cultural barriers can be overcome by establishing standardized collection workflows, multidisciplinary collaboration, and external partnerships. Our experience provides a practical framework for other centers seeking to participate in pediatric CNS tumor liquid biopsy research.

Neuro-Oncology Pediatrics
Translational Genomics Research Institute (US), Center for Cancer and Blood Disorders (US), Phoenix Children's Hospital (US), Mayo Clinic in Arizona (US), Mayo Clinic Hospital (US), Mayo Clinic in Florida (US), A.T. Still University (US)
Good health and well-being, Partnerships for the goals
Openalex Percentile: Top 18%
Cancer Genomics and Diagnostics
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