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Minimal residual disease analysis by eight-color flow cytometry in relapsed childhood acute lymphoblastic leukemia
L. Karawajew, M. Dworzak, R. Ratei, P. Rhein, G. Gaipa, B. Buldini, G. Basso, O. Hrusak, WD. Ludwig, G. Henze, K. Seeger, A. von Stackelberg, E. Mejstrikova, C. Eckert,
Jazyk angličtina Země Itálie
Typ dokumentu klinické zkoušky, časopisecké články, práce podpořená grantem
Grantová podpora
NT13462
MZ0
CEP - Centrální evidence projektů
Digitální knihovna NLK
Plný text - Článek
Zdroj
NLK
Directory of Open Access Journals
od 1994
Free Medical Journals
od 1994
Freely Accessible Science Journals
od 1994
PubMed Central
od 2009
Europe PubMed Central
od 2009
Open Access Digital Library
od 1994-01-01
ROAD: Directory of Open Access Scholarly Resources
od 1996
- 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
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
Citace poskytuje Crossref.org
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