Evidence map›Paper›PMID 28324750›Full record

ReviewEuropean journal of cancer (Oxford, England : 1990)2017

Biological mechanisms of immune escape and implications for immunotherapy in head and neck squamous cell carcinoma.

Jennifer D Moy, Jessica M Moskovitz, Robert L Ferris

Abstract readReview
In one paragraph

Review in European journal of cancer (Oxford, England : 1990), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed, 1 pooled it
6.7field-weighted citation impact, top 2% 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

64 citing papers in PubMed, 1 synthesis or guideline pooled it, 106 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Immunotherapy in Head and Neck Cancer.Cancer treatment and research · 2025
    Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Review
  15. Immuno-oncology in head and neck squamous cell carcinoma - a narrative review.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2023
    Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Review

4 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

3 authors at 1 institution in 1 country.

Jennifer D MoyDepartment of Otolaryngology, University of Pittsburgh, Pittsburgh, PA, USA. Electronic address: moyjd@upmc.edu.
Jessica M MoskovitzDepartment of Otolaryngology, University of Pittsburgh, Pittsburgh, PA, USA.
Robert L FerrisDepartment of Otolaryngology, University of Pittsburgh, Pittsburgh, PA, USA; Department of Immunology, University of Pittsburgh, Pittsburgh, PA, USA; Cancer Immunology Program, University of Pittsburgh Cancer Institute, Pittsburgh, PA, USA.
University of Pittsburgh · US

Funding

WILD TYPE P53-BASED ADJUVANT IMMUNOTHERAPY FOR SCCHNP50CA097190 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Greg M. Delgoffe · 2004 to 2026
$49.6M
Postdoctoral Training in Head and Neck OncologyT32CA060397 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI ZEVALLOS, JOSE P. · 1994 to 2024
$2.7M
NCI NIH HHS P50 CA097190NCI NIH HHS T32 CA060397
6 · The paper itself

Abstract

Head and neck squamous cell carcinoma (HNSCC) is an aggressive malignancy with high morbidity and mortality. Despite advances in cytotoxic therapies and surgical techniques, overall survival (OS) has not improved over the past few decades. This emphasises the need for intense investigation into novel therapies with good tumour control and minimal toxicity. Cancer immunotherapy has led this endeavour, attempting to improve tumour recognition and expand immune responses against tumour cells. While various forms of HNSCC immunotherapy are in preclinical trials, the most promising direction thus far has been with monoclonal antibodies (mAbs), targeting growth factor and immune checkpoint receptors. Preclinical and early phase trials have shown unprecedented efficacy with minimal adverse effects. This article will review biological mechanisms of immune escape and implications for immunotherapy in HNSCC.

Indexed as

Antibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntigen PresentationAntigens, NeoplasmAntineoplastic AgentsB7-H1 AntigenCarcinoma, Squamous CellCTLA-4 AntigenHead and Neck NeoplasmsHumansImmunotherapyIpilimumabNivolumabProgrammed Cell Death 1 ReceptorSquamous Cell Carcinoma of Head and NeckT-LymphocytesAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntigens, NeoplasmAntineoplastic AgentsatezolizumabB7-H1 AntigenCD274 protein, humanCTLA-4 AntigendurvalumabIpilimumabNivolumabPDCD1 protein, humanpembrolizumabProgrammed Cell Death 1 ReceptorCheckpoint receptorsHead and neck cancerImmunotherapySquamous cell carcinoma

Identifiers

PMID28324750
PMCPMC5459368
OpenAlexW2596058531

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.