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doi: 10.1038/leu.2017.29
pmid: 28104919
pmc: PMC5629369
handle: 10366/136897 , 10261/169262 , 20.500.12530/41487 , 1887/116066
doi: 10.1038/leu.2017.29
pmid: 28104919
pmc: PMC5629369
handle: 10366/136897 , 10261/169262 , 20.500.12530/41487 , 1887/116066
Flow cytometry has become a highly valuable method to monitor minimal residual disease (MRD) and evaluate the depth of complete response (CR) in bone marrow (BM) of multiple myeloma (MM) after therapy. However, current flow-MRD has lower sensitivity than molecular methods and lacks standardization. Here we report on a novel next generation flow (NGF) approach for highly sensitive and standardized MRD detection in MM. An optimized 2-tube 8-color antibody panel was constructed in five cycles of design-evaluation-redesign. In addition, a bulk-lysis procedure was established for acquisition of ⩾107 cells/sample, and novel software tools were constructed for automatic plasma cell gating. Multicenter evaluation of 110 follow-up BM from MM patients in very good partial response (VGPR) or CR showed a higher sensitivity for NGF-MRD vs conventional 8-color flow-MRD -MRD-positive rate of 47 vs 34% (P=0.003)-. Thus, 25% of patients classified as MRD-negative by conventional 8-color flow were MRD-positive by NGF, translating into a significantly longer progression-free survival for MRD-negative vs MRD-positive CR patients by NGF (75% progression-free survival not reached vs 7 months; P=0.02). This study establishes EuroFlow-based NGF as a highly sensitive, fully standardized approach for MRD detection in MM which overcomes the major limitations of conventional flow-MRD methods and is ready for implementation in routine diagnostics.
Adult, Male, Neoplasm, Residual, Plasma Cells, Cell Count, Sensitivity and Specificity, EMC MM-02-72-01, Immunophenotyping, Specimen Handling, Multiple myeloma, Antibody Specificity, Next generation flow, Humans, Aged, Aged, 80 and over, Minimal residual disease, Equipment Design, Middle Aged, Flow Cytometry, Treatment Outcome, Oncology, Original Article, Female, Multiple Myeloma, Software
Adult, Male, Neoplasm, Residual, Plasma Cells, Cell Count, Sensitivity and Specificity, EMC MM-02-72-01, Immunophenotyping, Specimen Handling, Multiple myeloma, Antibody Specificity, Next generation flow, Humans, Aged, Aged, 80 and over, Minimal residual disease, Equipment Design, Middle Aged, Flow Cytometry, Treatment Outcome, Oncology, Original Article, Female, Multiple Myeloma, Software
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 583 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 0.1% | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 1% | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 0.1% |
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