Evidence map›Paper›PMID 25483688›Full record

ReviewHuman vaccines & immunotherapeutics2014

Pancreatic cancer: role of the immune system in cancer progression and vaccine-based immunotherapy.

Amedeo Amedei, Elena Niccolai, Domenico Prisco

Open access · bronzeAbstract readReview
In one paragraph

Review in Human vaccines & immunotherapeutics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

56 citing papers in PubMed, 82 citations in OpenAlex.

  1. Trial
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  12. The Expression of Non B Cell-Derived Immunoglobulins.Advances in experimental medicine and biology · 2024
    Review
  13. Review
  14. Association betweenCancers · 2023
    Article
  15. ENO1 promotes immunosuppression and tumor growth in pancreatic cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
    Article
  16. Article
  17. Intratumour microbiome of pancreatic cancer.World journal of gastrointestinal oncology · 2023
    Review
  18. Review
  19. Article
  20. 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

3 authors at 2 institutions in 1 country.

Amedeo Amedeia Department of Experimental and Clinical Internal Medicine ; University of Florence ; Florence , Italy.
Elena Niccolai
Domenico Prisco
Azienda Ospedaliero-Universitaria Careggi · ITUniversity of Florence · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pancreatic cancer (PC) is the 5th leading cause of cancer related death in the developed world with more than 260,000 deaths annually worldwide and with a dismal 5-year survival. Surgery is the only potential hope of cure for PC, but, unfortunately, only 20% PC patients is resectable at the time of diagnosis. Therapeutic research efforts have mainly focused on improvements in radio/ chemo treatments and to date, there are only a few chemotherapeutic agents that have shown to be effective against PC, including gemcitabine with or without abraxane as well as a combination of 5-FU, leucovorin, oxaliplatin and irinotecan (the so-called FOLFIRINOX regimen). The survival of patients treated with these regimens is marginal and hence we are in urgent need of novel therapeutic approaches to treat pancreatic cancer. The success of immunotherapeutic strategies in other cancers and various evidences that pancreatic adenocarcinoma elicits antitumor immune responses, suggest that immunotherapies can be a promising alternative treatment modality for this deadly disease. PC immunotherapy treatments include passive immunotherapeutic approaches, such as the use of effector cells generated in vitro, and active immunotherapeutic strategies, which goal is to stimulate an antitumor response in vivo, by means of vaccination. In this review, we describe the immune suppressive mechanisms of pancreatic cancer and discuss recent preclinical and clinical efforts toward PC immunotherapy, including passive approaches, such as the use of antibodies and active strategies (vaccination), with a special mention of most recent treatment with CRS-207 and GVAX.

Indexed as

Antibodies, MonoclonalAntigens, NeoplasmAntineoplastic AgentsCancer VaccinesDendritic CellsDisease ProgressionHumansImmune ToleranceImmunotherapyPancreatic NeoplasmsT-LymphocytesTumor EscapeAntibodies, MonoclonalAntigens, NeoplasmAntineoplastic AgentsCancer VaccinesGVAX vaccineAPC, Antigen Presenting CellsCEA, carcinoembryonic antigenclinical trialsCTL, Cytotoxic CD8 T cellsDCs, Dendritic CellsENO1, a-EnolasiIDO, Indoleamine 2,3-dioxygenaseimmune responseimmunotherapymAbs, monoclonal antibodiesMUC1, Mucin-1NK, Natural Killerpancreatic cancerPC, pancreatic cancerTh, T helperTregs, Regulatory T cellsvaccine

Identifiers

PMID25483688
PMCPMC4514060
OpenAlexW2041246138

What OpenQuestion holds

Textmetadata
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.