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Characterization of Cell-Free DNA Size Distribution in Osteosarcoma Patients. | LitMetric

AI Article Synopsis

  • Cell-free DNA (cfDNA) analysis can noninvasively predict outcomes in osteosarcoma by examining the size distribution of cfDNA fragments in patients compared to healthy donors.
  • A study involving 50 osteosarcoma patients found that their cfDNA fragments were significantly shorter than those of healthy individuals, offering a high rate of diagnostic accuracy (100% specificity and sensitivity).
  • The research concluded that shorter cfDNA fragments (≤150 bp) serve as important prognostic indicators and enhance the detection of mutations, potentially helping to identify patients with worse outcomes.

Article Abstract

Purpose: Cell-free DNA (cfDNA) analysis is a powerful tool for noninvasively predicting patient outcomes. We analyzed the size distribution of cfDNA and assessed its prognostic and diagnostic values in an osteosarcoma cohort.

Experimental Design: The fragment size distribution and level of cfDNA were analyzed in 15 healthy donors and 50 patients with osteosarcoma using automated capillary electrophoresis. The prognostic performance of cfDNA size analysis was assessed using univariate and multivariable analyses. By performing whole-genome sequencing of matched cfDNA and osteosarcoma tissue samples, we investigated the correlation between the size and mutation profiles of cfDNA and the mutation concordance between cfDNA and paired tissue tumors.

Results: The size of cfDNA fragments in patients with osteosarcoma was significantly shorter than in healthy donors, with the integrative analysis of size distribution and level of cfDNA achieving a high specificity and sensitivity of 100%. The short cfDNA fragment (150-bp cut-off) was an independent prognostic predictor in this osteosarcoma cohort [HR, 9.03; 95% confidence interval (CI), 1.13-72.20; P = 0.038]. Shortened cfDNA fragments were found to be a major source of mutations. Enrichment of cfDNA fragments with less than or equal to 150 bp by in silico size selection remarkedly improved the detection of copy-number variation signals up to 2.3-fold when compared with total cfDNA, with a higher concordance rate with matched osteosarcoma tissue.

Conclusions: This finding demonstrated the potential of cfDNA size profiling in the stratification of poor prognostic patients with osteosarcoma. The short fragments of cfDNA are a promising source for boosting the detection of significant mutations in osteosarcoma. See related commentary by Weiser et al., p. 2017.

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Source
http://dx.doi.org/10.1158/1078-0432.CCR-22-2912DOI Listing

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