Circulating tumour DNA is a promising biomarker for risk stratification of central chondrosarcoma with IDH1/2 and GNAS mutations

Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

DOI

  • Iben Lyskjær
  • Christopher Davies, University College London, Royal National Orthopaedic Hospital NHS Trust
  • ,
  • Anna Christina Strobl, University College London, Royal National Orthopaedic Hospital NHS Trust
  • ,
  • Joanna Hindley, Royal National Orthopaedic Hospital NHS Trust
  • ,
  • Steven James, Royal National Orthopaedic Hospital NHS Trust
  • ,
  • Radhesh K. Lalam, Royal National Orthopaedic Hospital NHS Trust
  • ,
  • William Cross, University College London
  • ,
  • Geoff Hide, Newcastle upon Tyne Hospitals NHS Foundation Trust
  • ,
  • Kenneth S. Rankin, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle University
  • ,
  • Lee Jeys, Royal National Orthopaedic Hospital NHS Trust
  • ,
  • Roberto Tirabosco, Royal National Orthopaedic Hospital NHS Trust
  • ,
  • Jonathan Stevenson, Royal National Orthopaedic Hospital NHS Trust
  • ,
  • Paul O’Donnell, University College London, Royal National Orthopaedic Hospital NHS Trust
  • ,
  • Paul Cool, The Robert Jones and Agnes Hunt Orthopaedic and District Hospital NHS Trust, Keele University
  • ,
  • Adrienne M. Flanagan, University College London, Royal National Orthopaedic Hospital NHS Trust
  • ,
  • Genomics England Research Consortium

Chondrosarcoma (CS) is a rare tumour type and the most common primary malignant bone cancer in adults. The prognosis, currently based on tumour grade, imaging and anatomical location, is not reliable, and more objective biomarkers are required. We aimed to determine whether the level of circulating tumour DNA (ctDNA) in the blood of CS patients could be used to predict outcome. In this multi-institutional study, we recruited 145 patients with cartilaginous tumours, of which 41 were excluded. ctDNA levels were assessed in 83 of the remaining 104 patients, whose tumours harboured a hotspot mutation in IDH1/2 or GNAS. ctDNA was detected pre-operatively in 31/83 (37%) and in 12/31 (39%) patients postoperatively. We found that detection of ctDNA was more accurate than pathology for identification of high-grade tumours and was associated with a poor prognosis; ctDNA was never associated with CS grade 1/atypical cartilaginous tumours (ACT) in the long bones, in neoplasms sited in the small bones of the hands and feet or in tumours measuring less than 80 mm. Although the results are promising, they are based on a small number of patients, and therefore, introduction of this blood test into clinical practice as a complementary assay to current standard-of-care protocols would allow the assay to be assessed more stringently and developed for a more personalised approach for the treatment of patients with CS.

Original languageEnglish
JournalMolecular Oncology
Volume15
Issue12
Pages (from-to)3679-3690
Number of pages12
ISSN1574-7891
DOIs
Publication statusPublished - Dec 2021
Externally publishedYes

Bibliographical note

© 2021 The Authors. Molecular Oncology published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies.

    Research areas

  • chondrosarcoma, circulating tumour DNA, GNAS, IDH1, IDH2, prognosis

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