Improved flow cytometric detection of minimal residual disease in childhood acute lymphoblastic leukemia

被引:0
作者
B Denys
A J van der Sluijs-Gelling
C Homburg
C E van der Schoot
V de Haas
J Philippé
R Pieters
J J M van Dongen
V H J van der Velden
机构
[1] Erasmus MC,Department of Immunology
[2] University Medical Center,Department of Clinical Chemistry
[3] Microbiology and Immunology,Department of Experimental Immunohematology
[4] Ghent University Hospital,Department of Pediatric Oncology/Hematology
[5] Dutch Childhood Oncology Group,undefined
[6] Sanquin,undefined
[7] Erasmus MC-Sophia Childrens Hospital,undefined
来源
Leukemia | 2013年 / 27卷
关键词
acute lymphoblastic leukemia; childhood; minimal residual disease; flow cytometry; real-time quantitative PCR;
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摘要
Most current treatment protocols for acute lymphoblastic leukemia (ALL) include minimal residual disease (MRD) diagnostics, generally based on PCR analysis of rearranged antigen receptor genes. Although flow cytometry (FCM) can be used for MRD detection as well, discordant FCM and PCR results are obtained in 5–20% of samples. We evaluated whether 6-color FCM, including additional markers and new marker combinations, improved the results. Bone marrow samples were obtained from 363 ALL patients at day 15, 33 and 78 and MRD was analyzed using 6-color (218 patients) or 4-color (145 patients) FCM in parallel to routine PCR-based MRD diagnostics. Compared with 4-color FCM, 6-color FCM significantly improved the concordance with PCR-based MRD data (88% versus 96%); particularly the specificity of the MRD analysis improved. However, PCR remained more sensitive at levels <0.01%. MRD-based risk groups were similar between 6-color FCM and PCR in 68% of patients, most discrepancies being medium risk by PCR and standard risk by FCM. Alternative interpretation of the PCR data, aimed at prevention of false-positive MRD results, changed the risk group to standard risk in half (52%) of these discordant cases. In conclusion, 6-color FCM significantly improves MRD analysis in ALL but remains less sensitive than PCR-based MRD-diagnostics.
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页码:635 / 641
页数:6
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