Minimal residual disease analysis by eight-color flow cytometry in relapsed childhood acute lymphoblastic leukemia
Jazyk angličtina Země Itálie Médium print-electronic
Typ dokumentu klinické zkoušky, časopisecké články, práce podpořená grantem
PubMed
26001791
PubMed Central
PMC4486228
DOI
10.3324/haematol.2014.116707
PII: haematol.2014.116707
Knihovny.cz E-zdroje
- MeSH
- B-lymfocyty účinky léků imunologie patologie MeSH
- CD antigeny genetika imunologie MeSH
- DNA-nukleotidylexotransferasa genetika imunologie MeSH
- exprese genu MeSH
- imunofenotypizace MeSH
- kojenec MeSH
- kostní dřeň účinky léků imunologie patologie MeSH
- lidé MeSH
- nádorové biomarkery genetika imunologie MeSH
- polymerázová řetězová reakce MeSH
- pre-B-buněčná leukemie diagnóza farmakoterapie genetika patologie MeSH
- předškolní dítě MeSH
- protinádorové látky terapeutické užití MeSH
- protoonkogenní proteiny c-bcl-2 genetika imunologie MeSH
- průtoková cytometrie metody MeSH
- recidiva MeSH
- reziduální nádor MeSH
- Check Tag
- kojenec MeSH
- lidé MeSH
- předškolní dítě MeSH
- Publikační typ
- časopisecké články MeSH
- klinické zkoušky MeSH
- práce podpořená grantem MeSH
- Názvy látek
- BCL2 protein, human MeSH Prohlížeč
- CD antigeny MeSH
- DNA-nukleotidylexotransferasa MeSH
- nádorové biomarkery MeSH
- protinádorové látky MeSH
- protoonkogenní proteiny c-bcl-2 MeSH
Multiparametric flow cytometry is an alternative approach to the polymerase chain reaction method for evaluating minimal residual disease in treatment protocols for primary acute lymphoblastic leukemia. Given considerable differences between primary and relapsed acute lymphoblastic leukemia treatment regimens, flow cytometric assessment of minimal residual disease in relapsed leukemia requires an independent comprehensive investigation. In the present study we addressed evaluation of minimal residual disease by flow cytometry in the clinical trial for childhood relapsed acute lymphoblastic leukemia using eight-color flow cytometry. The major challenge of the study was to reliably identify low amounts of residual leukemic cells against the complex background of regeneration, characteristic of follow-up samples during relapse treatment. In a prospective study of 263 follow-up bone marrow samples from 122 patients with B-cell precursor acute lymphoblastic leukemia, we tested various B-cell markers, adapted the antibody panel to the treatment protocol, and evaluated its performance by a blinded parallel comparison with the polymerase chain reaction data. The resulting eight-color single-tube panel showed a consistently high overall concordance (P<0.001) and, under optimal conditions, sensitivity similar to that of the reference polymerase chain reaction method. Overall, evaluation of minimal residual disease by flow cytometry can be successfully integrated into the clinical management of relapsed childhood acute lymphoblastic leukemia either as complementary to the polymerase chain reaction or as an independent risk stratification tool. ALL-REZ BFM 2002 clinical trial information: NCT00114348.
Department of Pediatric Oncology Hematology Charité Universitätsmedizin Berlin Germany
Laboratory of Pediatric Onco Hematology Department of Pediatrics University Hospital of Padova Italy
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ClinicalTrials.gov
NCT00114348