Relapsed rhabdoid tumours and other non-nephroblastoma childhood and adolescent kidney tumours: perspectives from the HARMONICA collaboration
Document Type
Journal Article
Publication Date
1-2-2026
Journal
Nature reviews. Urology
DOI
10.1038/s41585-025-01117-4
Abstract
Paediatric kidney tumours are generally associated with a favourable survival rate. Most children are diagnosed with Wilms tumour, which has a 90% long-term survival rate with conventional front-line and salvage therapies. However, treatments and outcomes of children with relapsed non-Wilms tumours, such as malignant rhabdoid tumour of the kidney, renal-cell carcinoma (including renal medullary carcinoma), clear-cell sarcoma of the kidney, anaplastic sarcoma of the kidney and congenital mesoblastic nephroma are not well defined. Several of these non-Wilms tumours include unfavourable prognostic subtypes. Currently available data on non-Wilms tumours support advancing studies that pivot from conventional strategies towards disease-specific, biologically driven novel treatments to improve outcomes for each of these rare childhood kidney tumours.
APA Citation
Ortiz, Michael V.; Wens, Francis S.; Hong, Andrew L.; Quarello, Paola; Verschuur, Arnauld C.; Tracy, Elisabeth T.; Daw, Najat C.; Dome, Jeffrey S.; Walz, Amy L.; Sprokkerieft, Julia; Tytgat, Godelieve A.; Kentsis, Alex; Libes-Bander, Jaime; Schoettler, Peter J.; Perotti, Daniela; Drost, Jarno; Venkatramani, Rajkumar; Geller, James I.; and van den Heuvel-Eibrink, Marry M., "Relapsed rhabdoid tumours and other non-nephroblastoma childhood and adolescent kidney tumours: perspectives from the HARMONICA collaboration" (2026). GW Authored Works. Paper 8629.
https://hsrc.himmelfarb.gwu.edu/gwhpubs/8629
Department
Pediatrics