Evidence map›Paper›PMID 29871670›Full record

ArticleJournal for immunotherapy of cancer2018

Immune oncology, immune responsiveness and the theory of everything.

Tolga Turan, Deepti Kannan, Maulik Patel, J Matthew Barnes, Sonia G Tanlimco, Rongze Lu, Kyle Halliwill, Sarah Kongpachith, Douglas E Kline, Wouter Hendrickx and 7 more

Abstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 1 pooled it
–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

43 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  20. Contextual reprogramming of CAR-T cells for treatment of HER2Journal of translational medicine · 2021
    Article
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

17 authors.

Tolga TuranImmune-Oncology Discovery, AbbVie, Redwood City, CA, USA.
Deepti KannanImmune-Oncology Discovery, AbbVie, Redwood City, CA, USA.
Maulik PatelClinical Pharmacology and Pharmacometrics, Abbvie, Redwood City, CA, USA.
J Matthew BarnesImmune-Oncology Discovery, AbbVie, Redwood City, CA, USA.
Sonia G TanlimcoImmune-Oncology Discovery, AbbVie, Redwood City, CA, USA.
Rongze LuImmune-Oncology Discovery, AbbVie, Redwood City, CA, USA.
Kyle HalliwillImmune-Oncology Discovery, AbbVie, Redwood City, CA, USA.
Sarah KongpachithImmune-Oncology Discovery, AbbVie, Redwood City, CA, USA.
Douglas E KlineImmune-Oncology, AbbVie, North Chicago, IL, USA.
Wouter HendrickxTumor Biology, Immunology, and Therapy Section, Division of Translational Medicine, Research Branch, Sidra Medical and Research Center, Doha, Qatar.
Alessandra CesanoNanostring Technologies, Inc., Seattle, WA, USA.
Lisa H ButterfieldUPMC Hillman Cancer Center, University of Pittsburgh, Pittsburgh, PA, USA.
Howard L KaufmanDepartments of Surgery and Medicine, Rutgers University, New Jersey, NJ, USA.
Thomas J HudsonImmune-Oncology Discovery, AbbVie, Redwood City, CA, USA.
Davide BedognettiTumor Biology, Immunology, and Therapy Section, Division of Translational Medicine, Research Branch, Sidra Medical and Research Center, Doha, Qatar.
Francesco MarincolaImmune-Oncology Discovery, AbbVie, Redwood City, CA, USA.
Josue SamayoaImmune-Oncology Discovery, AbbVie, Redwood City, CA, USA. josue.samayoa@abbvie.com.ORCID 0000-0003-3609-8954

Funding

MOLECULAR &CELLULAR IMMUNOBIOLOGYT32AI007290 · NIAID · STANFORD UNIVERSITY · PI Sean Curtis Bendall, Olivia M Martinez · 1985 to 2026
$27.0M
NIAID NIH HHS T32 AI007290
6 · The paper itself

Abstract

Anti-cancer immunotherapy is encountering its own checkpoint. Responses are dramatic and long lasting but occur in a subset of tumors and are largely dependent upon the pre-existing immune contexture of individual cancers. Available data suggest that three landscapes best define the cancer microenvironment: immune-active, immune-deserted and immune-excluded. This trichotomy is observable across most solid tumors (although the frequency of each landscape varies depending on tumor tissue of origin) and is associated with cancer prognosis and response to checkpoint inhibitor therapy (CIT). Various gene signatures (e.g. Immunological Constant of Rejection - ICR and Tumor Inflammation Signature - TIS) that delineate these landscapes have been described by different groups. In an effort to explain the mechanisms of cancer immune responsiveness or resistance to CIT, several models have been proposed that are loosely associated with the three landscapes. Here, we propose a strategy to integrate compelling data from various paradigms into a "Theory of Everything". Founded upon this unified theory, we also propose the creation of a task force led by the Society for Immunotherapy of Cancer (SITC) aimed at systematically addressing salient questions relevant to cancer immune responsiveness and immune evasion. This multidisciplinary effort will encompass aspects of genetics, tumor cell biology, and immunology that are pertinent to the understanding of this multifaceted problem.

Indexed as

ImmunotherapyNeoplasmsHumansImmune ToleranceCancer immunotherapyCheckpoint inhibitorsImmune resistance

Identifiers

PMID29871670
PMCPMC5989400

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.