Evidence map›Paper›PMID 26313665›Full record

ArticleBritish journal of cancer2015

Stromal infiltration of CD8 T cells is associated with improved clinical outcome in HPV-positive oropharyngeal squamous carcinoma.

K Oguejiofor, J Hall, C Slater, G Betts, G Hall, N Slevin, S Dovedi, P L Stern, C M L West

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 96 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
96citing papers in PubMed, 2 pooled it
4.3field-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

96 citing papers in PubMed, 2 syntheses or guidelines pooled it, 150 citations in OpenAlex.

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36 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

9 authors at 3 institutions in 2 countries.

K OguejioforTranslational Radiobiology Group, Institute of Cancer Sciences, Manchester Academic Health Science Centre, University of Manchester, Wilmslow Road, Manchester, UK.
J HallLymphoma Translational Research Group, Institute of Cancer Sciences, Manchester Academic Health Science Centre, University of Manchester, Wilmslow Road, Manchester, UK.
C SlaterLymphoma Translational Research Group, Institute of Cancer Sciences, Manchester Academic Health Science Centre, Manchester Medical School, University of Manchester, Wilmslow Road, Manchester, UK.
G BettsCentral Manchester University Hospitals, Manchester, UK.
G HallCentral Manchester University Hospitals, Manchester, UK.
N SlevinThe Christie NHS Foundation Trust, Manchester, Wilmslow Road, UK.
S DovediTargeted Therapy Group, Institute of Cancer Sciences, Manchester Academic Health Science Centre, the University of Manchester; Wilmslow Road, Manchester.
P L SternCenter for Women's Cancer, Institute of Cancer Sciences, University of Manchester, Paterson Building, Wilmslow Road, Manchester, M20 4BX, UK.
C M L WestTranslational Radiobiology Group, Institute of Cancer Sciences, Manchester Academic Health Science Centre, University of Manchester, Wilmslow Road, Manchester, UK.
University of Manchester · GBManchester Academic Health Science Centre · GBThe Christie NHS Foundation Trust · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPatients with human papillomavirus (HPV)-positive oropharyngeal squamous cell carcinoma (OPSCC) have a better prognosis than those with HPV-negative tumours. There is interest in de-escalating their treatment but strategies are needed for risk stratification to identify subsets with a poor prognosis. This study investigated tumour-infiltrating lymphocytes (TILs) in relation to HPV tumour status and patient survival.

methodsBiopsies from 218 patients diagnosed with OPSCC between 2002 and 2011, who underwent chemo/radiotherapy were analysed for HPV by PCR, in-situ hybridisation and p16 immunohistochemistry (IHC). One hundred and thirty-nine samples with concordant HPV detection were analysed for CD3, CD4, CD8 and FoxP3 expression in tumour and stromal regions using multiplexIHC and multispectral image analysis. Labelling of smooth muscle actin (SMA) identified activated stroma.

resultsHuman papillomavirus-positive compared with HPV-negative OPSCC had higher infiltration in both tumour and stromal areas of CD4 and CD8 T cells but not FoxP3 T regulatory cells. Only CD3+CD8+ stromal and not tumour area infiltration was associated with increased survival (P=0.02). There was significantly higher SMA expression in HPV-positive compared with -negative tumours, which did not correlate with survival.

conclusionsStudies of TILs for risk stratification in OPSCC should assess stromal infiltration.

Indexed as

Lymphocytes, Tumor-InfiltratingActinsAntigens, NeoplasmBiopsyCarcinoma, Squamous CellCD3 ComplexCD4 AntigensCD4-Positive T-LymphocytesCD8 AntigensCD8-Positive T-LymphocytesForkhead Transcription FactorsHumansImmunohistochemistryLymphocyte SubsetsMuscle, SmoothOropharyngeal NeoplasmsActinsAntigens, NeoplasmCD3 ComplexCD4 AntigensCD8 AntigensForkhead Transcription FactorsFOXP3 protein, human

Identifiers

PMID26313665
PMCPMC4578081
OpenAlexW1645587630

What OpenQuestion holds

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Registered trials

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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.