Evidence map›Paper›PMID 30319627›Full record

ReviewFrontiers in immunology2018

The Potential of CAR T Cell Therapy in Pancreatic Cancer.

Mehmet Akce, Mohammad Y Zaidi, Edmund K Waller, Bassel F El-Rayes, Gregory B Lesinski

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 85 papers.

0numbers the graph read from it
0cells of the map it votes in
85citing papers in PubMed
5.6field-weighted citation impact, top 3% 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

85 citing papers in PubMed, 154 citations in OpenAlex.

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  12. CAR-T cell therapy: a game-changer in cancer treatment and beyond.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
    Review
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25 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

5 authors at 2 institutions in 1 country.

Mehmet AkceDepartment of Hematology and Oncology, Winship Cancer Institute, Emory University School of Medicine, Atlanta, GA, United States.
Mohammad Y ZaidiDepartment of General Surgery, Indiana University, Bloomington, IN, United States.
Edmund K WallerDepartment of Hematology and Oncology, Winship Cancer Institute, Emory University School of Medicine, Atlanta, GA, United States.
Bassel F El-RayesDepartment of Hematology and Oncology, Winship Cancer Institute, Emory University School of Medicine, Atlanta, GA, United States.
Gregory B LesinskiDepartment of Hematology and Oncology, Winship Cancer Institute, Emory University School of Medicine, Atlanta, GA, United States.
Emory University · USIndiana University Bloomington · US

Funding

Winship Cancer Institute Cancer Center Support GrantP30CA138292 · NCI · EMORY UNIVERSITY · PI Suresh S Ramalingam · 2009 to 2026
$47.5M
Enhancing immune therapy in pancreatic cancer by targeting IL-6R01CA208253 · NCI · OHIO STATE UNIVERSITY · PI LESINSKI, GREGORY B. · 2016 to 2021
$1.6M
NCI NIH HHS P30 CA138292NCI NIH HHS R01 CA208253
6 · The paper itself

Abstract

Pancreatic cancer has a dismal prognosis and effective treatment options are limited. It is projected to be the second most common cause of cancer related mortality in the United States by 2030 and there is urgent unmet need for novel systemic treatment options. Immunotherapy with antibodies targeting PD-1, PD-L1, CTLA-4 has not shown clinical activity in unselected pancreatic cancer, emphasizing the need for combination immunotherapy approaches or other therapeutic strategies. As such, chimeric antigen receptor (CAR) T cell therapy represents an emerging therapeutic option for pancreatic cancer. This modality utilizes genetically engineered T cells that are redirected to specific cancer-associated antigens to elicit potent cytotoxic activity. This review summarizes the available preclinical data and highlights early phase clinical trials using CAR T cell approaches in pancreatic cancer, a disease state that is gaining attention as a conduit for cell therapy. Future directions in application of CAR T cell therapy are also considered including its ability to be directed against novel epitopes and combined with other therapeutic regimens.

Indexed as

AnimalsClinical Trials, Phase I as TopicClinical Trials, Phase II as TopicCombined Modality TherapyDisease Models, AnimalEpitopes, T-LymphocyteHumansImmunotherapy, AdoptivePancreatic NeoplasmsProtein EngineeringReceptors, Chimeric AntigenTreatment OutcomeTumor MicroenvironmentEpitopes, T-LymphocyteReceptors, Chimeric Antigenadoptive T cell therapyCAR T cellsgenetically engineered T cellsmesothelinpancreas cancer

Identifiers

PMID30319627
PMCPMC6167429
OpenAlexW2890610945

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.