Evidence map›Paper›PMID 25092812›Full record

ReviewCancer immunology research2014

Vaccines for cancer prevention: a practical and feasible approach to the cancer epidemic.

Olivera J Finn

Open access · bronzeAbstract readReview
In one paragraph

Review in Cancer immunology research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
3.3field-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

37 citing papers in PubMed, 66 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Personalized cancer vaccines: adjuvants are important, too.Cancer immunology, immunotherapy : CII · 2018
    Review
  14. Review
  15. Article
  16. Review
  17. The dawn of vaccines for cancer prevention.Nature reviews. Immunology · 2018
    Review
  18. A Believer's Overview of Cancer Immunosurveillance and Immunotherapy.Journal of immunology (Baltimore, Md. : 1950) · 2018
    Review
  19. Article
  20. Article
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

1 author at 1 institution in 1 country.

Olivera J FinnDepartment of Immunology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania OJFINN@pitt.edu.
University of Pittsburgh · US

Funding

T CELL IMMUNITY TO EPITHELIAL TUMOR MUCINSR01CA056103 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI FINN, OLIVERA J · 1991 to 2013
$3.4M
Dendritic Cell Biology and TherapyR01CA168392 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI FINN, OLIVERA J · 2011 to 2015
$2.0M
NCI NIH HHS CA168392NCI NIH HHS CA5613NCI NIH HHS R01 CA056103NCI NIH HHS R01 CA168392
6 · The paper itself

Abstract

Concerted efforts of tumor immunologists over more than two decades contributed numerous well-defined tumor antigens, many of which were promptly developed into cancer vaccines and tested in animal models and in clinical trials. Encouraging results from animal models were seldom recapitulated in clinical trials. The impediment to greater success of these vaccines has been their exclusive use for cancer therapy. What clinical trials primarily revealed were the numerous ways in which cancer and/or standard treatments for cancer could suppress the patient's immune system, making it very difficult to elicit effective immunity with therapeutic vaccines. In contrast, there is an extensive database of information from experiments in appropriate animal models showing that prophylactic vaccination is highly effective and safe. There are also studies that show that healthy people have immune responses against antigens expressed on tumors, some generated in response to viral infections and others in response to various nonmalignant acute inflammatory events. These immune responses do not appear to be dangerous and do not cause autoimmunity. Epidemiology studies have shown that these immune responses may reduce cancer risk significantly. Vaccines based on tumor antigens that are expressed differentially between tumors and normal cells and can stimulate immunity, and for which safety and efficacy have been proved in animal models and to the extent possible in therapeutic clinical trials, should be considered prime candidates for prophylactic cancer vaccines.

Indexed as

AnimalsCancer VaccinesEpidemicsHumansNeoplasmsPrecision MedicineCancer Vaccines

Identifiers

PMID25092812
PMCPMC4163937
OpenAlexW1984120155

What OpenQuestion holds

Textmetadata
LicenceTDM
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.