Abstract

Liquid biopsies are emerging as an alternative source for pediatric cancer biomarkers with potential applications during all stages of patient care, from diagnosis to long-term follow-up. While developments within this field are reported, these mainly focus on dedicated items such as a specific liquid biopsy matrix, analyte, and/or single tumor type. To the best of our knowledge, a comprehensive overview is lacking. Here, we review the current state of liquid biopsy research for the most common non-central nervous system pediatric solid tumors. These include neuroblastoma, renal tumors, germ cell tumors, osteosarcoma, Ewing sarcoma, rhabdomyosarcoma and other soft tissue sarcomas, and liver tumors. Within this selection, we discuss the most important or recent studies involving liquid biopsy-based biomarkers, anticipated clinical applications, and the current challenges for success. Furthermore, we provide an overview of liquid biopsy-based biomarker publication output for each tumor type based on a comprehensive literature search between 1989 and 2023. Per study identified, we list the relevant liquid biopsy-based biomarkers, matrices (e.g., peripheral blood, bone marrow, or cerebrospinal fluid), analytes (e.g., circulating cell-free and tumor DNA, microRNAs, and circulating tumor cells), methods (e.g., digital droplet PCR and next-generation sequencing), the involved pediatric patient cohort, and proposed applications. As such, we identified 344 unique publications. Taken together, while the liquid biopsy field in pediatric oncology is still behind adult oncology, potentially relevant publications have increased over the last decade. Importantly, steps towards clinical implementation are rapidly gaining ground, notably through validation of liquid biopsy-based biomarkers in pediatric clinical trials.

Details

Title
A comprehensive overview of liquid biopsy applications in pediatric solid tumors
Author
Janssen, Ferdinand W. 1   VIAFID ORCID Logo  ; Lak, Nathalie S. M. 1 ; Janda, Claudia Y. 1 ; Kester, Lennart A. 1 ; Meister, Michael T. 2   VIAFID ORCID Logo  ; Merks, Johannes H. M. 3   VIAFID ORCID Logo  ; van den Heuvel-Eibrink, Marry M. 4   VIAFID ORCID Logo  ; van Noesel, Max M. 3 ; Zsiros, Jozsef 1   VIAFID ORCID Logo  ; Tytgat, Godelieve A. M. 5 ; Looijenga, Leendert H. J. 6   VIAFID ORCID Logo 

 Princess Máxima Center, Utrecht, the Netherlands (GRID:grid.487647.e) 
 Princess Máxima Center, Utrecht, the Netherlands (GRID:grid.487647.e); Oncode Institute, Utrecht, the Netherlands (GRID:grid.499559.d) 
 Princess Máxima Center, Utrecht, the Netherlands (GRID:grid.487647.e); University of Utrecht, Division of Imaging and Oncology, University Medical Center Utrecht, Utrecht, the Netherlands (GRID:grid.5477.1) (ISNI:0000000120346234) 
 Princess Máxima Center, Utrecht, the Netherlands (GRID:grid.487647.e); University of Utrecht, Wilhelmina Children’s Hospital-Division of CHILDHEALTH, University Medical Center Utrech, Utrecht, the Netherlands (GRID:grid.5477.1) (ISNI:0000000120346234) 
 Princess Máxima Center, Utrecht, the Netherlands (GRID:grid.487647.e); University of Utrecht, Department of Genetics, University Medical Center Utrecht, Utrecht, the Netherlands (GRID:grid.5477.1) (ISNI:0000000120346234) 
 Princess Máxima Center, Utrecht, the Netherlands (GRID:grid.487647.e); University of Utrecht, Department of Pathology, University Medical Center Utrecht, Utrecht, the Netherlands (GRID:grid.5477.1) (ISNI:0000000120346234) 
Pages
172
Publication year
2024
Publication date
2024
Publisher
Nature Publishing Group
ISSN
2397768X
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
3087605041
Copyright
© The Author(s) 2024. corrected publication 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.