ctDNA monitoring shows promise but faces genomic hurdles in sarcoma subtypes
The study reports on the evolving clinical utility of circulating tumor DNA (ctDNA) across multiple sarcoma subtypes, including gastrointestinal stromal tumor, leiomyosarcoma, rhabdomyosarcoma, osteosarcoma, and Ewing sarcoma. Investigators note that while technical advances have improved rare ctDNA detection in other cancers, sarcoma genomic complexity and heterogeneity continue to pose significant analytical challenges. The review outlines current evidence for ctDNA applications in monitoring recurrence and guiding therapy, emphasizing that standardized analytical workflows and rigorous validation will be required before liquid biopsy can be integrated into routine sarcoma diagnostics.
The original study
Current Evidence for Circulating Tumor DNA in Sarcoma: Challenges and Opportunities for Clinical Application.
- Authors
- Goodsell KE, Carter JA, Abrams HR, Mogal H, Loggers ET, Sharib J
- Journal
- Journal of surgical oncology
- Type
- Journal Article, Review
- PMID
- 42437510
Original abstract
Sarcomas represent a diverse group of mesenchymal tumors with high rates of recurrence after resection. While recent technical advances have enabled the detection of rare circulating tumor DNA (ctDNA) in other malignancies, the complexity and heterogeneity of sarcoma genomics have historically limited ctDNA in these cancers. This narrative review highlights the rapidly evolving evidence supporting potential clinical applications of ctDNA in common sarcoma subtypes including gastrointestinal stromal tumor, leiomyosarcoma, rhabdomyosarcoma, osteosarcoma, and Ewing sarcoma.