Evidence map›Paper›PMID 35129050›Full record

ArticleCancer biology & therapy2022

Targeting gastrointestinal cancers with chimeric antigen receptor (CAR)-T cell therapy.

Ross E Staudt, Robert D Carlson, Adam E Snook

Open access · goldAbstract read
In one paragraph

Article in Cancer biology & therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.0field-weighted citation impact, top 12% 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

11 citing papers in PubMed, 20 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

3 authors at 1 institution in 1 country.

Ross E StaudtDepartment of Pharmacology & Experimental Therapeutics, Thomas Jefferson University, Philadelphia, PA, USA.ORCID 0000-0003-1439-7937
Robert D CarlsonDepartment of Pharmacology & Experimental Therapeutics, Thomas Jefferson University, Philadelphia, PA, USA.ORCID 0000-0001-7770-6894
Adam E SnookDepartment of Pharmacology & Experimental Therapeutics, Thomas Jefferson University, Philadelphia, PA, USA.ORCID 0000-0001-9216-4560
Thomas Jefferson University · US

Funding

Training Program in Cancer BiologyT32CA236736 · NCI · THOMAS JEFFERSON UNIVERSITY · PI APLIN, ANDREW ERIC, LANGUINO, LUCIA R. · 2019 to 2023
$1.1M
NCI NIH HHS T32 CA236736
6 · The paper itself

Abstract

The immune system is capable of remarkably potent and specific efficacy against infectious diseases. For decades, investigators sought to leverage those characteristics to create immune-based therapies (immunotherapy) that might be far more effective and less toxic than conventional chemotherapy and radiation therapy for cancer. Those studies revealed many factors and mechanisms underlying the success or failure of cancer immunotherapy, leading to synthetic biology approaches, including CAR-T cell therapy. In this approach, patient T cells are genetically modified to express a chimeric antigen receptor (CAR) that converts T cells of any specificity into tumor-specific T cells that can be expanded to large numbers and readministered to the patient to eliminate cancer cells, including bulky metastatic disease. This approach has been most successful against hematologic cancers, resulting in five FDA approvals to date. Here, we discuss some of the most promising attempts to apply this technology to cancers of the gastrointestinal tract.

Indexed as

Gastrointestinal NeoplasmsImmunotherapy, AdoptiveReceptors, Chimeric AntigenHumansReceptors, Antigen, T-CellReceptors, Antigen, T-CellReceptors, Chimeric AntigenCAR-T cell therapychimeric antigen receptor (CAR)colorectal canceresophageal cancergastric cancergastrointestinal cancerImmunotherapy

Identifiers

PMID35129050
PMCPMC8820794
OpenAlexW4210522106

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.