Evidence map›Paper›PMID 30181329›Full record

ReviewMolecular cancer therapeutics2018

Strategies to Address Chimeric Antigen Receptor Tonic Signaling.

Adam Ajina, John Maher

Open access · bronzeAbstract readReview
In one paragraph

Review in Molecular cancer therapeutics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 157 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
157citing papers in PubMed, 2 pooled it
7.5field-weighted citation impact, top 2% 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

157 citing papers in PubMed, 2 syntheses or guidelines pooled it, 228 citations in OpenAlex.

  1. Pooled it
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  17. CD147 regulates CD8iScience · 2026
    Article
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97 more citing papers are in PubMed but not listed here.

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

2 authors at 1 institution in 1 country.

Adam AjinaCAR Mechanics Group, King's College London, London, United Kingdom. adam.ajina@nhs.net.
John MaherCAR Mechanics Group, King's College London, London, United Kingdom.
Guy's Hospital · GB

Funding

Cancer Research UK C11499/A21623Department of HealthMedical Research Council MR/M024733/1Medical Research Council MR/R001936/1Wellcome TrustWellcome Trust 104802/Z/14/Z
6 · The paper itself

Abstract

Adoptive cell transfer using chimeric antigen receptors (CAR) has emerged as one of the most promising new therapeutic modalities for patients with relapsed or refractory B-cell malignancies. Thus far, results in patients with advanced solid tumors have proven disappointing. Constitutive tonic signaling in the absence of ligand is an increasingly recognized complication when deploying these synthetic fusion receptors and can be a cause of poor antitumor efficacy, impaired survival, and reduced persistence

Indexed as

Cell DifferentiationHumansImmunotherapy, AdoptiveLeukemia, Lymphocytic, Chronic, B-CellReceptors, Antigen, T-CellReceptors, Chimeric AntigenRecombinant Fusion ProteinsSignal TransductionT-LymphocytesReceptors, Antigen, T-CellReceptors, Chimeric AntigenRecombinant Fusion Proteins

Identifiers

PMID30181329
PMCPMC6130819
OpenAlexW2889691274

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.