Evidence map›Paper›PMID 26487586›Full record

ArticleAnnals of oncology : official journal of the European Society for Medical Oncology2016

Comprehensive serum cytokine analysis identifies IL-1RA and soluble IL-2Rα as predictors of event-free survival in T-cell lymphoma.

M Gupta, M Stenson, M O'Byrne, M J Maurer, T Habermann, J R Cerhan, G W Weiner, T E Witzig

Open access · bronzeAbstract read
In one paragraph

Article in Annals of oncology : official journal of the European Society for Medical Oncology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

23 citing papers in PubMed, 39 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 4 institutions in 1 country.

M GuptaDivision of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester gupta.mamta@mayo.edu.
M StensonDivision of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester.
M O'ByrneDepartment of Health Sciences Research, Mayo Clinic, Rochester, USA.
M J MaurerDepartment of Health Sciences Research, Mayo Clinic, Rochester, USA.
T HabermannDivision of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester.
J R CerhanDepartment of Health Sciences Research, Mayo Clinic, Rochester, USA.
G W WeinerDepartment of Internal Medicine, University of Iowa College of Medicine, Iowa City, USA.
T E WitzigDivision of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester.
Mayo Clinic in Florida · USWinnMed · USMayo Clinic · USUniversity of Iowa · US

Funding

Viral VectorP30CA086862 · NCI · UNIVERSITY OF IOWA · PI Douglas Robert Spitz · 2000 to 2026
$70.0M
The Role of Monocytes in non-Hodgkin LymphomaP50CA097274 · NCI · UNIVERSITY OF IOWA · PI WEINER, GEORGE J. · 2002 to 2021
$45.7M
Molecular Epidemiology of NHL and CLLR01CA092153 · NCI · MAYO CLINIC ROCHESTER · PI CERHAN, JAMES R · 2003 to 2012
$6.7M
Signal transduction inhibitor therapy for LymphomaR01CA127433 · NCI · MAYO CLINIC ROCHESTER · PI WITZIG, THOMAS E. · 2007 to 2011
$1.7M
NCI NIH HHS P50 CA97274NCI NIH HHS R01 CA127433NCI NIH HHS R01 CA92153
6 · The paper itself

Abstract

backgroundT-cell malignancies are heterogeneous in their clinical presentation and pathology, and have a poor prognosis. New biomarkers are needed to predict prognosis and to provide insights into signal pathways used by these cells. The goal of this study was to evaluate pretreatment serum cytokines in patients with newly diagnosed T-cell neoplasms and correlate with clinical outcome. PATIENTS AND

methodsWe evaluated 30 cytokines in pretreatment serum from 68 untreated patients and 14 normal controls. Significantly elevated cytokines were correlated with patterns of abnormalities, event-free survival (EFS) and overall survival (OS).

resultsOur data demonstrated significantly elevated levels (versus controls) of seven cytokines-epidermal growth factor (EGF), IL-6, IL-12, interferon gamma-induced protein (IP)-10, soluble interleukin (sIL)-2Rα, monokine induced by gamma interferon (MIG), and IL-1RA-in all T-cell neoplasms (P < 0.05). In the angioimmunoblastic subset, all seven cytokines except IP-10 and in the peripheral T-cell lymphoma (TCL)-not otherwise specified subset, only IP-10, sIL-2Rα, MIG, and IL-8 were statistically elevated compared with control. Of these, elevated cytokines all but EGF were predictive of an inferior EFS; IL-1RA, sIL-2Rα, and MIG predicted an inferior OS. In a multivariate analysis, sIL-2Rα [hazard ratio (HR) = 3.95; 95% confidence interval (CI) 1.61-8.38] and IL-1RA (HR = 3.28; 95% CI 1.47-7.29) levels remained independent predictors of inferior EFS. TCL cell lines secreted high levels of sIL-2Rα and expressed the IL-2Rα surface receptor.

conclusionsThis report describes the cytokines relevant to prognosis in patients with untreated TCL and provides the rationale to include serum IL-1RA and sIL-2Rα as biomarkers in future trials. Inhibition of these cytokines may also be of therapeutic benefit.

Indexed as

AdultAgedAged, 80 and overBiomarkers, TumorCase-Control StudiesCell Line, TumorDisease-Free SurvivalFemaleHumansInterleukin 1 Receptor Antagonist ProteinInterleukin-2 Receptor alpha SubunitKaplan-Meier EstimateLymphoma, T-CellMaleMiddle AgedPrognosisBiomarkers, TumorInterleukin 1 Receptor Antagonist ProteinInterleukin-2 Receptor alpha SubunitAITLcytokinesIL-1RAPTCL-NOSsIL-2RαT-cell lymphoma

Identifiers

PMID26487586
PMCPMC4684152
OpenAlexW1751498211

What OpenQuestion holds

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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.