Tumor biology, biomarkers, and liquid biopsy in pediatric renal tumors

Author:

Walz Amy L.1,Maschietto Mariana2ORCID,Crompton Brian3,Evageliou Nicholas4,Dix David5,Tytgat Godelieve6ORCID,Gessler Manfred78ORCID,Gisselsson David9ORCID,Daw Najat C.10,Wegert Jenny8

Affiliation:

1. Division of Hematology, Oncology, Neuro‐Oncology, and Stem Cell Transplant Ann & Robert H. Lurie Children's Hospital of Chicago Chicago Illinois USA

2. Research Center Boldrini Children's Hospital Campinas São Paulo Brazil

3. Department of Pediatric Oncology Dana‐Farber/Harvard Cancer Center Dana Farber Cancer Institute Boston Massachusetts USA

4. Division of Oncology Children's Hospital of Philadelphia Philadelphia Pennsylvania USA

5. British Columbia Children's Hospital Vancouver British Columbia Canada

6. Princess Máxima Center for Pediatric Oncology CS Utrecht The Netherlands

7. Comprehensive Cancer Center Mainfranken Wuerzburg Germany

8. Theodor‐Boveri‐Institute/Biocenter Developmental Biochemistry University of Wuerzburg Wuerzburg Germany

9. Cancer Cell Evolution Unit Division of Clinical Genetics Department of Laboratory Medicine Lund University Lund Sweden

10. Division of Pediatrics The University of Texas MD Anderson Cancer Center Houston Texas USA

Abstract

AbstractThe expansion of knowledge regarding driver mutations for Wilms tumor (WT) and malignant rhabdoid tumor of the kidney (MRT) and various translocations for other pediatric renal tumors opens up new possibilities for diagnosis and treatment. In addition, there are growing data surrounding prognostic factors that can be used to stratify WT treatment to improve outcomes. Here, we review the molecular landscape of WT and other pediatric renal tumors as well as WT prognostic factors. We also review incorporation of circulating tumor DNA/liquid biopsies to leverage this molecular landscape, with potential use in the future for distinguishing renal tumors at the time of diagnosis and elucidating intratumor heterogeneity, which is not well evaluated with standard biopsies. Incorporation of liquid biopsies will require longitudinal collection of multiple biospecimens. Further preclinical research, identification and validation of biomarkers, molecular studies, and data sharing among investigators are crucial to inform therapeutic strategies that improve patient outcomes.

Funder

University of Texas MD Anderson Cancer Center

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

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