Detection of residual B precursor lymphoblastic leukemia by uniform gating flow cytometry
Language English Country United States Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
19760767
DOI
10.1002/pbc.22261
Knihovny.cz E-resources
- MeSH
- Child MeSH
- Gene Rearrangement MeSH
- Remission Induction MeSH
- Humans MeSH
- Polymerase Chain Reaction MeSH
- Precursor B-Cell Lymphoblastic Leukemia-Lymphoma diagnosis genetics MeSH
- Prognosis MeSH
- Flow Cytometry * MeSH
- Receptors, Antigen, T-Cell genetics MeSH
- Neoplasm, Residual diagnosis genetics MeSH
- Check Tag
- Child MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Receptors, Antigen, T-Cell MeSH
BACKGROUND: Residual disease (RD) is an important prognostic factor in acute lymphoblastic leukemia (ALL). Flow cytometry (FC)-based RD detection is easy to perform, but interpretation requires expert analysis due to individual differences among patients. PROCEDURE: We focused at the design of standardized and reproducible RD monitoring in ALL. RD was investigated by a uniform gating strategy, which was designed internationally and tested in one center by Ig/TCR rearrangements. RESULTS: For each gate, positivity cutoff value was assigned using quantification of non-leukemic background. Comparing to Ig/TCR at 0.1% level, 80 of 103 specimens were correctly diagnosed by FC. The predictive value of FC RD at day 15 was then analyzed. In B lineage ALL, day 15 FC significantly correlated with Ig/TCR results at day 33 and/or week 12 (P < 0.01). No significant correlation was found in T lineage ALL. CONCLUSIONS: Thus, FC with preset uniform gating at day 15 predicts PCR-detectable MRD in B precursor ALL. Presented data may be used to define new polychromatic cytometric diagnostics of MRD including semiautomatic assessment. Pediatr Blood Cancer 2010; 54:62-70. (c) 2009 Wiley-Liss, Inc.
References provided by Crossref.org
High-resolution Antibody Array Analysis of Childhood Acute Leukemia Cells