Evidence map›Paper›PMID 21472850›Full record

ArticleCytometry. Part B, Clinical cytometry2011

Improved ZAP-70 assay using two clones, multiple methods of analysis and clinical correlation.

Heba A Degheidy, David J Venzon, Mohammed Z H Farooqui, Fatima Abbasi, Diane C Arthur, Wyndham H Wilson, Adrian Wiestner, M A Stetler-Stevenson, Gerald E Marti

Open access · hybridAbstract read
In one paragraph

Article in Cytometry. Part B, Clinical cytometry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 27% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Combined normal donor and CLL: Single tube ZAP-70 analysis.Cytometry. Part B, Clinical cytometry · 2012
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Heba A DegheidyDivision of Cellular, Tissue and Gene Therapies, Center for Biologics Evaluation and Research, Food & Drug Administration, 8800 Rockville Pike, Bethesda, MD 20892, USA.
David J Venzon
Mohammed Z H Farooqui
Fatima Abbasi
Diane C Arthur
Wyndham H Wilson
Adrian Wiestner
M A Stetler-Stevenson
Gerald E Marti
Center for Biologics Evaluation and Research · USNational Heart Lung and Blood Institute · USNational Institutes of Health · US

Funding

Tumor microenvironment in CLL and MCL: pathogenesis, targets, and therapyZIAHL002346 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI WIESTNER, ADRIAN U · 2009 to 2025
$29.8M
Flow Cytometric Analysis of Benign and Malignant TumorsZICSC009372 · NCI · DIVISION OF CLINICAL SCIENCES - NCI · PI WANG, HAO-WEI · 2009 to 2025
$29.6M
Office of Collaborative BiostatisticsZIDSC007202 · NCI · DIVISION OF CLINICAL SCIENCES - NCI · PI CHOO-WOSOBA, HYOYOUNG · 2009 to 2025
$14.5M
Therapeutic Strategies and Molecular Correlates in Aggressive B-cell LymphomasZIASC006741 · NCI · DIVISION OF CLINICAL SCIENCES - NCI · PI WILSON, WYNDHAM H · 2009 to 2025
$10.4M
Flow Cytometric Evaluation of BiomarkersZICBC011104 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI WANG, HAO-WEI · 2009 to 2025
$8.6M
Cytogenetic Studies of B-cell Chronic Lymphocytic Leukemia (B-CLL)ZIASC010282 · NCI · DIVISION OF CLINICAL SCIENCES - NCI · PI ARTHUR, DIANE C · 2009 to 2016
$1.1M
Intramural NIH HHS ZIA HL002346
6 · The paper itself

Abstract

introductionIn a companion methodological study, we compared two anti-ZAP-70 clones (1E7.2 AF 488 and SBZAP PE) and four selected methods of analysis. Clinical correlations are required for validation.

methodsMulticolor flow-cytometric evaluation of ZAP-70, CD38, CD69, CD26, CD49d, and CD27 was tested in 45 untreated-CLL patients. Four methods of ZAP-70 expression analysis and a scoring system were designed. A correlation analysis between ZAP-70 score, immunoglobulin heavy chain variable (IGHV) mutational status, fluorescence in situ hybridization, and these biomarkers was undertaken.

resultsThere is a strong correlation between ZAP-70 expression and IGHV mutational status. The scoring system for a single reagent (P = 0.0006 or 0.0002) favors the use of multiple methods of analysis. The combined score was substantially equivalent (P = 0.0003). There was also a correlation with del 13q14 (P = 0.017) and trisomy12 (P = 0.011). A correlation for CD38 and ZAP-70 score was seen using both 1E7.2 AF488 and SBZAP PE when ≥20% or ≥7% cutoff was used. A positive correlation was seen for CD49d expression using both reagents. CD26 showed a correlation with ZAP-70 expression, but it was dependent upon the method of analysis. CD69 and CD27 showed no statistically significant correlation.

conclusionIn our study population, ZAP-70 expression is the better predictor of the IGHV mutational status. The correlation analysis confirms that the use of four methods of analysis with a single reagent or both reagents is superior to the use of a single method of analysis. The routine use of CD38, CD49d, and CD26 will require standardization.

Indexed as

Immunoglobulin Heavy ChainsLeukemia, Lymphocytic, Chronic, B-CellZAP-70 Protein-Tyrosine KinaseAgedAged, 80 and overAntibodies, MonoclonalAntigens, SurfaceBiomarkers, TumorFemaleFlow CytometryGene ExpressionHumansImmunoassayIn Situ Hybridization, FluorescenceMaleMiddle AgedAntibodies, MonoclonalAntigens, SurfaceBiomarkers, TumorImmunoglobulin Heavy ChainsZAP-70 Protein-Tyrosine Kinase

Identifiers

PMID21472850
PMCPMC3407415
OpenAlexW2125746336

What OpenQuestion holds

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LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.