Evidence map›Paper›PMID 23563514›Full record

ReviewHuman vaccines & immunotherapeutics2013

Cancer vaccines: identification of biomarkers predictive of clinical efficacy.

Richard Harrop

Open access · bronzeAbstract readReview
In one paragraph

Review in Human vaccines & immunotherapeutics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 37% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Trial
  2. Review
  3. 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 2 countries.

Richard HarropOxford BioMedica (UK) Ltd.; The Medawar Centre; Oxford, UK.
Science Oxford · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Personalized medicine is playing an increasingly important role in the treatment of patients living with cancer. This landmark shift has been driven in part by statistics emerging from the "one size fits all" approach to the treatment of cancer patients. Some reports suggest that only a minority of individuals actually benefit from treatment and adverse effects of medications remain a major cause of hospitalization, morbidities and deaths. Although the side-effect profile of most immunotherapy treatment modalities is usually fairly benign, there is no reason to believe that immunotherapy is any different from other oncology therapies in that some patients are likely to receive more benefit than others. Indeed, the fact that generation of the therapeutic modality requires translation through multiple complex biological processes for an immunotherapy product to be effective may mean that such approaches require an even better understanding of the patient being treated. Furthermore, the very low success rate of cancer immunotherapy approaches to deliver benefit to patients demands a more detailed understanding of who will benefit and why. The identification of biomarkers predictive of treatment benefit is one route to improve the success rate of cancer vaccines.

Indexed as

BiomarkersCancer VaccinesHumansImmunotherapyNeoplasmsBiomarkersCancer Vaccinescancerimmune responsepredictive biomarkertherapeutic vaccinetumor antigen

Identifiers

PMID23563514
PMCPMC3903898
OpenAlexW2105288572

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.