Measurable Residual Disease Monitoring in Lymphoma
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cancer Research,Oncology,Hematology
Link
https://link.springer.com/content/pdf/10.1007/s11899-023-00715-6.pdf
Reference102 articles.
1. Cheson BD, et al. Recommendations for initial evaluation, staging, and response assessment of Hodgkin and non-Hodgkin lymphoma: the Lugano classification. J Clin Oncol. 2014;32:3059–67. https://doi.org/10.1200/jco.2013.54.8800.
2. Ansell SM, Armitage JO. Positron emission tomographic scans in lymphoma: convention and controversy. Mayo Clin Proc. 2012;87:571–80. https://doi.org/10.1016/j.mayocp.2012.03.006.
3. Scherer F, et al. High-throughput sequencing for noninvasive disease detection in hematologic malignancies. Blood. 2017;130:440–52. https://doi.org/10.1182/blood-2017-03-735639.
4. Taylor SC, Laperriere G, Germain H. Droplet digital PCR versus qPCR for gene expression analysis with low abundant targets: from variable nonsense to publication Quality Data. Sci Rep. 2017:7. https://doi.org/10.1038/s41598-017-02217-x.
5. •Ching T, et al. Analytical evaluation of the CLONOSEQ assay for establishing measurable (minimal) residual disease in acute lymphoblastic leukemia, chronic lymphocytic leukemia, and multiple myeloma. BMC Cancer. 2020;20 https://doi.org/10.1186/s12885-020-07077-9. Provides evidence for the justification of using ClonoSeq for MRD monitoring in a variety of hematologic malignancies. This was the first FDA approved NGS-based assay for this indication and remains a commonly utilized tool for this purpose.
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