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Updated: Feb 11, 2026

Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
Published on: April 4, 2018
Complementary Roles of Next-Generation Flow and Next-Generation Sequencing for Measurable Residual Disease Assessment
Min-Seung Park1, Dae Jin Lim2,3, Hee-Jin Kim2
1Department of Laboratory Medicine, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, Korea.
Next-generation flow (NGF)-MRD and next-generation sequencing (NGS)-MRD assays are vital for multiple myeloma (MM) monitoring. Combined MRD negativity predicts better progression-free survival, highlighting the importance of both assays.
Area of Science:
- Hematology
- Oncology
- Molecular Diagnostics
Background:
- Measurable residual disease (MRD) assays are crucial for prognosis and treatment guidance in multiple myeloma (MM).
- Comparing next-generation flow (NGF)-MRD and next-generation sequencing (NGS)-MRD assays is essential for optimizing patient management.
Purpose of the Study:
- To compare the diagnostic performance and clinical utility of NGF-MRD and NGS-MRD assays in MM patients.
- To evaluate the prognostic value of MRD detection by both NGF and NGS methods.
Main Methods:
- Evaluated 55 bone marrow samples from 41 MM patients for MRD.
- NGF-MRD performed on fresh samples; NGS-MRD performed on archived DNA using LymphoTrack® IGH FR1 assay.
Main Results:
- MRD detection rates were 43.6% for NGF-MRD and 29.1% for NGS-MRD, with 67.3% concordance.
- Combined MRD negativity by both assays was associated with significantly better 3-year progression-free survival (75.9%) compared to MRD positivity (40.0%, P=0.035).
- Revised International Staging System stage III and combined MRD positivity were strongly associated with PFS.
Conclusions:
- Both NGF-MRD and NGS-MRD play critical, complementary roles in monitoring MM.
- Isolated MRD positivity by either method can indicate disease progression, emphasizing the value of both assays.
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