Evidence map›Paper›PMID 27105079›Full record

ArticleLeukemia & lymphoma2016

Immunophenotypic and diagnostic characterization of angioimmunoblastic T-cell lymphoma by advanced flow cytometric technology.

Sanam Loghavi, Sa A Wang, L Jeffrey Medeiros, Jeffrey L Jorgensen, Xin Li, Zijun Y Xu-Monette, Roberto N Miranda, Ken H Young

Open access · greenAbstract read
In one paragraph

Article in Leukemia & lymphoma, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

16 citing papers in PubMed, 58 citations in OpenAlex.

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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

8 authors at 1 institution in 1 country.

Sanam Loghavia Department of Hematopathology , The University of Texas, MD Anderson Cancer Center , Houston , TX , USA.
Sa A Wanga Department of Hematopathology , The University of Texas, MD Anderson Cancer Center , Houston , TX , USA.
L Jeffrey Medeirosa Department of Hematopathology , The University of Texas, MD Anderson Cancer Center , Houston , TX , USA.
Jeffrey L Jorgensena Department of Hematopathology , The University of Texas, MD Anderson Cancer Center , Houston , TX , USA.
Xin Lia Department of Hematopathology , The University of Texas, MD Anderson Cancer Center , Houston , TX , USA.
Zijun Y Xu-Monettea Department of Hematopathology , The University of Texas, MD Anderson Cancer Center , Houston , TX , USA.
Roberto N Mirandaa Department of Hematopathology , The University of Texas, MD Anderson Cancer Center , Houston , TX , USA.
Ken H Younga Department of Hematopathology , The University of Texas, MD Anderson Cancer Center , Houston , TX , USA.
The University of Texas MD Anderson Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
P4 -TARGETING MULTIPLE MYELOMA BY COMBINING CDK INHIBITORS AND BCL-2 ANTAGONISTSP50CA142509 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KWAK, LARRY W · 2010 to 2014
$11.1M
Convergence of MicroRNAs and p53 Signaling in Multiple Myeloma: Environmental CoR01CA138688 · NCI · UNIVERSITY OF LOUISVILLE · PI LI, YONG · 2009 to 2017
$2.9M
UT M.D. Anderson Cancer Center Lymphoma SPOREP50CA136411 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KWAK, LARRY W · 2009 to 2011
$1.5M
Deep Sequencing of Small Regulatory RNAs in Diffuse Large B cell LymphomaRC1CA146299 · NCI · SCRIPPS RESEARCH INSTITUTE, THE · PI XIAO, CHANGCHUN · 2009 to 2010
$1000k
NCI NIH HHS P30 CA016672NCI NIH HHS P50 CA136411NCI NIH HHS P50 CA142509NCI NIH HHS R01 CA138688NCI NIH HHS RC1 CA146299
6 · The paper itself

Abstract

Angioimmunoblastic T-cell lymphoma (AITL) often shows systemic symptoms related to immune dysregulation and cytokine production. Biopsy usually harbors few malignant cells in an abundant reactive background, which can be diagnostically challenging in cases with small biopsies. This study was performed to assess the value of flow cytometry (FC) and to determine the immunophenotypic alterations in 155 samples from 38 patients with AITL. FC detected an aberrant T-cell population in 97 of 155 samples that represented 0.5-90% of lymphocytes. Blood was involved in 11 of 16 patients. The most frequent immunophenotypic aberrancies included loss of CD3; altered T-cell receptor expression and aberrant CD10 expression. Altered CD3 expression was more frequently seen in peripheral blood (PB) and bone marrow (BM), whereas aberrant CD10 expression was more common in lymph node (LN). AITL cells often exhibit abnormal CD4

Indexed as

ImmunophenotypingAdultAgedAged, 80 and overBiomarkersBone Marrow CellsFemaleFlow CytometryGene Rearrangement, T-LymphocyteHumansLymph NodesLymphoma, T-CellMaleMiddle AgedNeoplasm StagingReceptors, Antigen, T-CellBiomarkersReceptors, Antigen, T-CellAITLangioimmunoblasticCD10CD3CHOPflow cytometryT-cell lymphomaTCR

Identifiers

PMID27105079
PMCPMC5142610
OpenAlexW2339514676

What OpenQuestion holds

Textmetadata
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.