Evidence map›Paper›PMID 32942747›Full record

ReviewCells2020

HNSCC: Tumour Antigens and Their Targeting by Immunotherapy.

Adrian von Witzleben, Chuan Wang, Simon Laban, Natalia Savelyeva, Christian H Ottensmeier

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
4.4field-weighted citation impact, top 4% 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

63 citing papers in PubMed, 89 citations in OpenAlex.

  1. Article
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  15. CELSR3 is a prognostic marker in HNSCC and correlates with immune cell infiltration in the tumor microenvironment.European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery · 2024
    Article
  16. Tumor Antigens beyond the Human Exome.International journal of molecular sciences · 2024
    Review
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3 more citing papers are in PubMed but not listed here.

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 2 countries.

Adrian von WitzlebenCancer Sciences Unit, Faculty of Medicine, University of Southampton, Southampton SO16 6YD, UK.ORCID 0000-0001-6766-4758
Chuan WangHead and Neck Center, Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool L69 7ZX, UK.
Simon LabanDepartment of Otorhinolaryngology, Head & Neck Surgery, University of Ulm, 89081 Ulm, Germany.ORCID 0000-0001-6732-7137
Natalia SavelyevaCancer Sciences Unit, Faculty of Medicine, University of Southampton, Southampton SO16 6YD, UK.
Christian H OttensmeierCancer Sciences Unit, Faculty of Medicine, University of Southampton, Southampton SO16 6YD, UK.ORCID 0000-0003-3619-1657
Universität Ulm · DEUniversity of Liverpool · GBUniversity of Southampton · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Head and neck squamous cell carcinomas (HNSCC) are a heterogeneous group of malignant tumours typically caused by alcohol and tobacco consumption, although an increasing number of HNSCC arise due to persistent infection with high-risk human papilloma virus (HPV). The treatment of HNSCC remains challenging, and the first-line setting is focused on surgery and chemoradiotherapy. A substantial proportion of HNSCC patients die from their disease, especially those with recurrent and metastatic disease. Among factors linked with good outcome, immune cell infiltration appears to have a major role. HPV-driven HNSCC are often T-cell rich, reflecting the presence of HPV antigens that are immunogenic. Tumour-associated antigens that are shared between patients or that are unique to an individual person may also induce varying degrees of immune response; studying these is important for the understanding of the interaction between the host immune system and the cancer. The resulting knowledge is critical for the design of better immunotherapies. Key questions are: Which antigens lead to an adaptive immune response in the tumour? Which of these are exploitable for immunotherapy? Here, we review the current thinking regarding tumour antigens in HNSCC and what has been learned from early phase clinical trials.

Indexed as

Antigens, Viral, TumorHead and Neck NeoplasmsHumansImmunotherapyLymphocytes, Tumor-InfiltratingPapillomaviridaePapillomavirus InfectionsSquamous Cell Carcinoma of Head and NeckT-LymphocytesAntigens, Viral, Tumorcancer antigenscancer testis antigensHNSCCHPVviral antigens

Identifiers

PMID32942747
PMCPMC7564543
OpenAlexW3085791571

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.