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    Liquid biopsies for residual disease and recurrence

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    Author
    Moss, Esther
    Keyword
    MRD
    RDR
    Clinical trials
    ctDNA
    Residual disease and recurrence
    Solid tumors
    Date
    2021-12-10
    
    Metadata
    Show full item record
    DOI
    10.1016/j.medj.2021.11.001
    Publisher's URL
    https://www.cell.com/med/fulltext/S2666-6340(21)00375-5?_returnURL=https%3A%2F%2Flinkinghub.elsevier.com%2Fretrieve%2Fpii%2FS2666634021003755%3Fshowall%3Dtrue
    Abstract
    Detection of minimal residual disease in patients with cancer, who are in complete remission with no cancer cells detectable, has the potential to improve recurrence-free survival through treatment selection. Studies analyzing circulating tumor DNA (ctDNA) in patients with solid tumors suggest the potential to accurately predict and detect relapse, enabling treatment strategies that may improve clinical outcomes. Over the past decade, assays for ctDNA detection in plasma samples have steadily increased in sensitivity and specificity. These are applied for the detection of residual disease after treatment and for earlier detection of recurrence. Novel clinical trials are now assessing how assays for "residual disease and recurrence" (RDR) may influence current treatment paradigms and potentially change the landscape of risk classification for cancer recurrence. In this review, we appraise the progress of RDR detection using ctDNA and consider the emerging role of liquid biopsy in the monitoring and management of solid tumors.
    Citation
    Wan, J. C. M., Mughal, T. I., Razavi, P., Dawson, S. J., Moss, E. L., Govindan, R., Tan, I. B., Yap, Y. S., Robinson, W. A., Morris, C. D., Besse, B., Bardelli, A., Tie, J., Kopetz, S., & Rosenfeld, N. (2021). Liquid biopsies for residual disease and recurrence. Med (New York, N.Y.), 2(12), 1292–1313. https://doi.org/10.1016/j.medj.2021.11.001
    Type
    Article
    URI
    http://hdl.handle.net/20.500.12904/16656
    Collections
    Cancer

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