Evidence map›Paper›PMID 32249277›Full record

ArticleBritish journal of cancer2020

Combining measures of immune infiltration shows additive effect on survival prediction in high-grade serous ovarian carcinoma.

Anne Montfort, Rowan J Barker-Clarke, Anna M Piskorz, Anna Supernat, Luiza Moore, Sarwah Al-Khalidi, Steffen Böhm, Paul Pharoah, Jacqueline McDermott, Frances R Balkwill and 1 more

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
5.2field-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

18 citing papers in PubMed, 32 citations in OpenAlex.

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  5. Overview of Tumor Heterogeneity in High-Grade Serous Ovarian Cancers.International journal of molecular sciences · 2023
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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

11 authors at 5 institutions in 2 countries.

Anne Montfort *Barts Cancer Institute, Queen Mary University of London, London, UK.
Rowan J Barker-Clarke *Cancer Research UK Cambridge Institute, Cambridge, UK.
Anna M PiskorzCancer Research UK Cambridge Institute, Cambridge, UK.
Anna SupernatLaboratory of Translational Oncology, Intercollegiate Faculty of Biotechnology, Medical University of Gdańsk, 80-211, Gdańsk, Poland.
Luiza MooreCancer Research UK Cambridge Institute, Cambridge, UK.
Sarwah Al-KhalidiCancer Research UK Cambridge Institute, Cambridge, UK.
Steffen BöhmBarts Cancer Institute, Queen Mary University of London, London, UK.
Paul PharoahCancer Research UK Cambridge Institute, Cambridge, UK.
Jacqueline McDermottBarts Cancer Institute, Queen Mary University of London, London, UK.
Frances R BalkwillBarts Cancer Institute, Queen Mary University of London, London, UK. f.balkwill@qmul.ac.uk.
James D BrentonCancer Research UK Cambridge Institute, Cambridge, UK. James.Brenton@cruk.cam.ac.uk.ORCID http://orcid.org/0000-0002-5738-6683
University of Cambridge · GBQueen Mary University of London · GBCancer Research UK Cambridge Center · GBGdańsk Medical University · PLUniversity College Hospital · GB

Funding

Cancer Research UK 16354Cancer Research UK 20265Cancer Research UK 22905Cancer Research UK 25714Cancer Research UK A15601Cancer Research UK A15973Cancer Research UK A16354Cancer Research UK A17197Cancer Research UK A22905Cancer Research UK A25714
6 · The paper itself

Abstract

backgroundIn colorectal and breast cancer, the density and localisation of immune infiltrates provides strong prognostic information. We asked whether similar automated quantitation and combined analysis of immune infiltrates could refine prognostic information in high-grade serous ovarian carcinoma (HGSOC) and tested associations between patterns of immune response and genomic driver alterations.

methodsEpithelium and stroma were semi-automatically segmented and the infiltration of CD45RO

resultsEpithelial CD8 [p = 0.027, hazard ratio (HR) = 0.83], stromal CD68 (p = 3 × 10

conclusionsCombining measures of immune infiltration provided improved survival modelling and evidence for the multiple effects of different immune factors on survival. The presence of stromal CD68

Indexed as

Cystadenocarcinoma, SerousFemaleHumansLymphocytes, Tumor-InfiltratingOvarian NeoplasmsPrognosisTumor Microenvironment

Identifiers

PMID32249277
PMCPMC7283353
OpenAlexW3015171468

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.