New Insights from Long-Term Clinical Use of Circulating Tumor DNA-Based Minimal Residual Disease Monitoring in Translocation-Associated Sarcomas
- Sophie Joch 1, Maria Anna Smolle 2, Karl Kashofer 3, Andrea Thüringer 3, Joanna Szkandera 4, Martin Benesch 5, Amin El-Heliebi 6,7, Bernadette Liegl-Atzwanger 3, Andreas Leithner 2, Markus G Seidel 5,8
- 1Division of Paediatric Haematology-Oncology, Department of Paediatrics and Adolescent Medicine, Medical University of Graz, Graz, Austria, sophie.joch@gmail.com.
- 2Department of Orthopaedics and Trauma, Medical University of Graz, Graz, Austria.
- 3Institute of Pathology, Medical University of Graz, Graz, Austria.
- 4Division of Oncology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
- 5Division of Paediatric Haematology-Oncology, Department of Paediatrics and Adolescent Medicine, Medical University of Graz, Graz, Austria.
- 6Division of Cell Biology, Histology and Embryology, Gottfried Schatz Research Center, Medical University of Graz, Graz, Austria.
- 7European Liquid Biopsy Society (ELBS), Hamburg, Germany.
- 8Styrian Children's Cancer Research Unit for Cancer and Inborn Errors of the Blood and Immunity in Children, Medical University of Graz, Graz, Austria.
- 0Division of Paediatric Haematology-Oncology, Department of Paediatrics and Adolescent Medicine, Medical University of Graz, Graz, Austria, sophie.joch@gmail.com.
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View abstract on PubMed
Summary
This summary is machine-generated.Monitoring circulating tumor DNA (ctDNA) effectively detects recurrence in translocation-associated sarcomas. While highly specific, ctDNA monitoring should complement imaging for complete recurrence detection.
Area Of Science
- Oncology
- Molecular Diagnostics
- Biomarker Research
Background
- Circulating tumor DNA (ctDNA) is increasingly used to monitor disease activity in translocation-associated tumors.
- Limited studies exist on the clinical application of ctDNA for monitoring minimal residual disease (MRD).
- This study assesses ctDNA's clinical utility as an MRD biomarker in translocation-associated sarcomas.
Purpose Of The Study
- To evaluate the clinical applicability of ctDNA for monitoring minimal residual disease (MRD).
- To correlate ctDNA levels with disease progression and recurrence in translocation-associated sarcomas.
- To determine the efficacy of ctDNA in early recurrence detection during patient follow-up.
Main Methods
- Retrospective analysis of 285 ctDNA samples from 34 patients with translocation-associated sarcoma.
- Correlation of ctDNA levels with clinical course and imaging data.
- Longitudinal blood sample collection over a median of 97 weeks (range: 7-398 weeks).
Main Results
- Significant association found between ctDNA levels and disease course (remission vs. progressive disease, p = 0.001).
- ctDNA levels were consistently higher in patients with multilocular recurrence (n=14) compared to unilocular recurrence (n=3).
- ctDNA remained undetectable in 3 cases of unilocular recurrence.
Conclusions
- ctDNA monitoring offers highly specific, additional information for early recurrence detection in translocation-associated sarcomas.
- ctDNA monitoring can be integrated into clinical practice for patient follow-up.
- Combined ctDNA quantification and conventional imaging are recommended for comprehensive MRD monitoring, as ctDNA alone may miss some unilocular recurrences.
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