Evidence map›Paper›PMID 32481570›Full record

ReviewCancers2020

Enhancing the Efficacy of CAR T Cells in the Tumor Microenvironment of Pancreatic Cancer.

Janina Henze, Frank Tacke, Olaf Hardt, Frauke Alves, Wa'el Al Rawashdeh

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.4field-weighted citation impact, top 9% 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

23 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
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  5. Building of CuOPharmaceutics · 2024
    Article
  6. Review
  7. Article
  8. Review
  9. Review
  10. Review
  11. Review
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  13. Combination therapy for pancreatic cancer: anti-PD-(L)1-based strategy.Journal of experimental & clinical cancer research : CR · 2022
    Review
  14. Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. Collagenase-ExpressingCancers · 2021
    Article
  20. Cell-Based Tracers as Trojan Horses for Image-Guided Surgery.International journal of molecular sciences · 2021
    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 3 institutions in 1 country.

Janina HenzeUniversity Medical Center Göttingen, Translational Molecular Imaging, Institute for Diagnostic and Interventional Radiology & Clinic for Hematology and Medical Oncology, 37075 Göttingen, Lower Saxony, Germany.
Frank TackeCharité University Medicine Berlin, Dept of Hepatology & Gastroenterology, 13353 Berlin, Germany.
Olaf HardtMiltenyi Biotec B.V. & Co. KG, R&D Reagents, Bergisch Gladbach, 51429 North Rhine-Westphalia, Germany.
Frauke AlvesUniversity Medical Center Göttingen, Translational Molecular Imaging, Institute for Diagnostic and Interventional Radiology & Clinic for Hematology and Medical Oncology, 37075 Göttingen, Lower Saxony, Germany.
Wa'el Al RawashdehMiltenyi Biotec B.V. & Co. KG, R&D Reagents, Bergisch Gladbach, 51429 North Rhine-Westphalia, Germany.
Miltenyi Biotec (Germany) · DECharité - Universitätsmedizin Berlin · DEUniversitätsmedizin Göttingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pancreatic cancer has the worst prognosis and lowest survival rate among all types of cancers and thus, there exists a strong need for novel therapeutic strategies. Chimeric antigen receptor (CAR)-modified T cells present a new potential option after successful FDA-approval in hematologic malignancies, however, current CAR T cell clinical trials in pancreatic cancer failed to improve survival and were unable to demonstrate any significant response. The physical and environmental barriers created by the distinct tumor microenvironment (TME) as a result of the desmoplastic reaction in pancreatic cancer present major hurdles for CAR T cells as a viable therapeutic option in this tumor entity. Cancer cells and cancer-associated fibroblasts express extracellular matrix molecules, enzymes, and growth factors, which can attenuate CAR T cell infiltration and efficacy. Recent efforts demonstrate a niche shift where targeting the TME along CAR T cell therapy is believed or hoped to provide a substantial clinical added value to improve overall survival. This review summarizes therapeutic approaches targeting the TME and their effect on CAR T cells as well as their outcome in preclinical and clinical trials in pancreatic cancer.

Indexed as

cancer-associated fibroblastsCAR T cell therapyextracellular matriximmunotherapypancreatic cancertumor microenvironment

Identifiers

PMID32481570
PMCPMC7353070
OpenAlexW3029201232

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.