Evidence map›Paper›PMID 38201305›Full record

ReviewCells2024

Chimeric Antigen Receptor T Cell Therapy for Pancreatic Cancer: A Review of Current Evidence.

Agata Czaplicka, Mieszko Lachota, Leszek Pączek, Radosław Zagożdżon, Beata Kaleta

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
9.9field-weighted citation impact, top 1% 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

29 citing papers in PubMed, 35 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Article
  13. Targeting orthotopic and metastatic pancreatic cancer with allogeneic stem cell-engineered mesothelin-redirected CAR-NKT cells.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  14. Pancreatic cancer in 2025: Have we found a solution?World journal of gastroenterology · 2025
    Review
  15. CAR-Macrophage Cell Therapy: A New Era of Hope for Pancreatic Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Review
  16. Review
  17. Review
  18. Review
  19. The Significance of Neuropilins in Gastrointestinal Cancers.International journal of molecular sciences · 2025
    Review
  20. From lab to lifesaver: the rise of CAR T-cell therapy in oncology.Journal of the Egyptian National Cancer Institute · 2025
    Review
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.

Agata CzaplickaDepartment of Internal Medicine and Gastroenterology, Mazovian "Bródnowski" Hospital, 03-242 Warsaw, Poland.
Mieszko LachotaLaboratory of Cellular and Genetic Therapies, Medical University of Warsaw, 02-091 Warsaw, Poland.ORCID 0000-0003-2808-8916
Leszek PączekDepartment of Clinical Immunology, Medical University of Warsaw, 02-006 Warsaw, Poland.ORCID 0000-0003-0160-3009
Radosław ZagożdżonLaboratory of Cellular and Genetic Therapies, Medical University of Warsaw, 02-091 Warsaw, Poland.ORCID 0000-0002-7957-2372
Beata KaletaDepartment of Clinical Immunology, Medical University of Warsaw, 02-006 Warsaw, Poland.ORCID 0000-0002-0697-2594
Medical University of Warsaw · PLGrochowski Hospital · PL

Funding

Foundation for Polish Science START PROGRAMMEMedical Research Agency 2020/ABM/04/00002-00
6 · The paper itself

Abstract

Chimeric antigen receptor (CAR) T-cell therapy has revolutionized the treatment of malignant and non-malignant disorders. CARs are synthetic transmembrane receptors expressed on genetically modified immune effector cells, including T cells, natural killer (NK) cells, or macrophages, which are able to recognize specific surface antigens on target cells and eliminate them. CAR-modified immune cells mediate cytotoxic antitumor effects via numerous mechanisms, including the perforin and granzyme pathway, Fas and Fas Ligand (FasL) pathway, and cytokine secretion. High hopes are associated with the prospective use of the CAR-T strategy against solid cancers, especially the ones resistant to standard oncological therapies, such as pancreatic cancer (PC). Herein, we summarize the current pre-clinical and clinical studies evaluating potential tumor-associated antigens (TAA), CAR-T cell toxicities, and their efficacy in PC.

Indexed as

Pancreatic NeoplasmsReceptors, Chimeric AntigenAntigens, SurfaceCell- and Tissue-Based TherapyHumansImmunotherapy, AdoptiveAntigens, SurfaceReceptors, Chimeric Antigenadoptive cell therapyCAR T cellschimeric antigen receptorimmunotherapypancreatic cancer

Identifiers

PMID38201305
PMCPMC10777940
OpenAlexW4390582318

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.