Evidence map›Paper›PMID 39093388›Full record

ArticleJournal of hematopathology2024

Quantification of the median fluorescence intensity of CD3 and CD4 in mycosis fungoides/Sezary syndrome versus non-neoplastic control cases in peripheral blood.

Fei Fei, Nivaz Brar, Melissa Beth Herring, Joshua R Menke, Jean Oak, Sebastian Fernandez-Pol

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Article in Journal of hematopathology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
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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

6 authors.

Fei FeiDepartment of Pathology, Stanford University School of Medicine, Stanford, CA, 94305, USA.
Nivaz BrarDepartment of Pathology, Stanford University School of Medicine, Stanford, CA, 94305, USA.
Melissa Beth HerringDepartment of Pathology, Stanford University School of Medicine, Stanford, CA, 94305, USA.
Joshua R MenkeDepartment of Pathology, Stanford University School of Medicine, Stanford, CA, 94305, USA.
Jean OakDepartment of Pathology, Stanford University School of Medicine, Stanford, CA, 94305, USA.
Sebastian Fernandez-PolDepartment of Pathology, Stanford University School of Medicine, Stanford, CA, 94305, USA. sfernand@stanford.edu.ORCID http://orcid.org/0000-0002-0428-0199

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Peripheral blood involvement by MF/SS has significant implications for prognosis and treatment. Flow cytometry is commonly used to assess MF/SS by analyzing the ratio of CD26- and/or CD7-CD4 + T cells and assessment of immunophenotypic abnormalities. However, distinguishing normal from abnormal cells is not always easy. In this study, we aimed to establish quantitative thresholds to better distinguish normal CD4 + T cells from neoplastic CD4 + T cells. A retrospective analysis of flow cytometry data was performed on 30 MF/SS patients with a detectable abnormal T cell population (positive), 63 patients with suspected or confirmed cutaneous involvement without a detectable abnormal T cell population (negative), and 60 healthy controls (control). CD3 and CD4 median fluorescence intensity (MFI) was normalized to internal control subsets. Among the positive cases, 50% had CD3 expression outside ± 2 SD from the mean of the negative and control group in the CD4 + CD26- subset. The corresponding specificity of this threshold was 94%. The ± 2 SD threshold showed a sensitivity of 57% and a specificity of 94% for the CD3 intensity among the CD7-negative subset. For CD4 intensity, the ± 2 SD threshold had a sensitivity of 33.3% and specificity of 95% for the CD26-negative subset and a sensitivity of 37% and specificity of 95% for the CD7-negative subset. In our study, although changes in CD3 and CD4 intensity greater than ± 2 SD were specific for MF/SS, more subtle differences in the intensity of CD3 and CD4 should not be used as the sole abnormality to make a diagnosis of circulating MF/SS.

Indexed as

CD3 ComplexCD4 AntigensCD4-Positive T-LymphocytesFlow CytometryMycosis FungoidesSezary SyndromeAdultAgedAged, 80 and overCase-Control StudiesFemaleHumansImmunophenotypingMaleMiddle AgedRetrospective StudiesCD3 ComplexCD4 AntigensMycosis fungoidesPeripheral bloodSezary syndrome

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Registered trials

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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.