Evidence map›Paper›PMID 40313965›Full record

Trial reportFrontiers in immunology2025

Influence of polyfunctional Tbet

Yeong Jer Lim, Andrew D Duckworth, Kim Clarke, Paul Kennedy, Indrani Karpha, Melanie Oates, Matthew Gornall, Nagesh Kalakonda, Joseph R Slupsky, Andrew R Pettitt

Registry-linked trialAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01678430 (A Randomised Investigation of Alternative Ofatumumab-containing Regimens in Less Fit Patients With CLL), which is not on this map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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.

NCT01678430 phase3unknown statusnot on this map

A Randomised Investigation of Alternative Ofatumumab-containing Regimens in Less Fit Patients With CLL

TypeinterventionalSponsorUniversity of LiverpoolRan2011 to 2017Enrolled670ConditionsChronic Lymphocytic LeukaemiaArmsOfatumumab, Chlorambucil, Bendamustine
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Yeong Jer LimDepartment of Molecular & Clinical Cancer Medicine, University of Liverpool, Liverpool, United Kingdom.
Andrew D DuckworthDepartment of Molecular & Clinical Cancer Medicine, University of Liverpool, Liverpool, United Kingdom.
Kim ClarkeComputational Biology Facility, University of Liverpool, Liverpool, United Kingdom.
Paul KennedyDepartment of Pharmacology & Therapeutics, University of Liverpool, Liverpool, United Kingdom.
Indrani KarphaDepartment of Molecular & Clinical Cancer Medicine, University of Liverpool, Liverpool, United Kingdom.
Melanie OatesDepartment of Molecular & Clinical Cancer Medicine, University of Liverpool, Liverpool, United Kingdom.
Matthew GornallLiverpool Clinical Trials Centre, University of Liverpool, Liverpool, United Kingdom.
Nagesh KalakondaDepartment of Molecular & Clinical Cancer Medicine, University of Liverpool, Liverpool, United Kingdom.
Joseph R SlupskyDepartment of Molecular & Clinical Cancer Medicine, University of Liverpool, Liverpool, United Kingdom.
Andrew R PettittDepartment of Molecular & Clinical Cancer Medicine, University of Liverpool, Liverpool, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: T-cell dysfunction is a hallmark of chronic lymphocytic leukemia (CLL), but the extent to which individual CD4 Methods: Pre-treatment blood samples from 138 CLL patients receiving initial chemoimmunotherapy containing bendamustine or chlorambucil in the NCRI RIAltO trial (NCT01678430; EudraCT 2011-000919-22) were subjected to deep immunophenotyping by mass cytometry using a bespoke panel of 37 antibodies. T-cell clusters were identified through unsupervised clustering and related to treatment outcomes. Additionally, a randomly selected cohort of 30 CLL patients underwent T-cell stimulation with anti-CD3/CD28 microbeads, followed by cytokine analysis using a separate 36-antibody panel, which included seven cytokines. Results: Seventeen CD4 Conclusion: Our study provides new insights into the potential for Tbet+ T-cell subpopulations to influence and predict specific clinical events in CLL. This, in turn, raises the possibility that these respective subpopulations could play an important role in controlling infection, solid tumours and CLL itself. Clinical Trial Registration: https://www.clinicaltrials.gov/, identifier NCT01678430; https://www.isrctn.com/ISRCTN09988575, identifier EudraCT 2011-000919-22.

Indexed as

CD4-Positive T-LymphocytesCD8-Positive T-LymphocytesLeukemia, Lymphocytic, Chronic, B-CellT-Lymphocyte SubsetsAdultAgedAged, 80 and overCytokinesFemaleHumansImmunophenotypingMaleMiddle AgedCytokinesbiomarkerchemoimmunotherapychronic lymphocytic leukaemia (CLL)Tbet/TBX21 transcription factorT cells

Identifiers

PMID40313965
PMCPMC12043603

What Socratic holds

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Registered trials

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 Socratic graph.