Evidence map›Paper›PMID 36095166›Full record

ArticleCancer immunology research2022

The Tumor Microenvironment of Clear-Cell Ovarian Cancer.

Michael-John Devlin, Rowan Miller, Florian Laforets, Panoraia Kotantaki, Dale W Garsed, Rebecca Kristeleit, David D Bowtell, Jacqueline McDermott, Eleni Maniati, Frances R Balkwill

Open access · hybridAbstract read
In one paragraph

Article in Cancer immunology research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
6.6field-weighted citation impact, top 3% 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

30 citing papers in PubMed, 41 citations in OpenAlex.

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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

10 authors at 6 institutions in 2 countries.

Michael-John DevlinBarts Cancer Institute, Queen Mary University of London, London, United Kingdom.ORCID 0000-0002-4481-1716
Rowan MillerDepartment of Medical Oncology, St Bartholomew's Hospital, London, United Kingdom.ORCID 0000-0002-2400-1716
Florian LaforetsBarts Cancer Institute, Queen Mary University of London, London, United Kingdom.ORCID 0000-0002-0924-5691
Panoraia KotantakiBarts Cancer Institute, Queen Mary University of London, London, United Kingdom.ORCID 0000-0003-1098-9994
Dale W GarsedPeter MacCallum Cancer Centre, Melbourne, Victoria, Australia.ORCID 0000-0003-1223-0121
Rebecca KristeleitMedical Oncology Department, Guy's and St Thomas' NHS Foundation Trust, London, United Kingdom.ORCID 0000-0003-3825-1326
David D BowtellPeter MacCallum Cancer Centre, Melbourne, Victoria, Australia.ORCID 0000-0001-9089-7525
Jacqueline McDermottDepartment of Surgery and Cancer, Imperial College London, London, United Kingdom.ORCID 0000-0001-8052-7133
Eleni ManiatiBarts Cancer Institute, Queen Mary University of London, London, United Kingdom.ORCID 0000-0001-6993-9890
Frances R BalkwillBarts Cancer Institute, Queen Mary University of London, London, United Kingdom.ORCID 0000-0002-5587-9759
Queen Mary University of London · GBPeter MacCallum Cancer Centre · AUGuy's and St Thomas' NHS Foundation Trust · GBImperial College London · GBSt Bartholomew's Hospital · GBUniversity College Hospital · GB

Funding

Cancer Research UK 25714Cancer Research UK A16354Cancer Research UK A25714Cancer Research UK C16420/A18066Cancer Research UK C355/A25137Medical Research Council MR/S00629×1Medical Research Council MR/S00629X/1
6 · The paper itself

Abstract

Some patients with advanced clear-cell ovarian cancer (CCOC) respond to immunotherapy; however, little is known about the tumor microenvironment (TME) of this relatively rare disease. Here, we describe a comprehensive quantitative and topographical analysis of biopsies from 45 patients, 9 with Federation Internationale des Gynaecologistes et Obstetristes (FIGO) stage I/II (early CCOC) and 36 with FIGO stage III/IV (advanced CCOC). We investigated 14 immune cell phenotype markers, PD-1 and ligands, and collagen structure and texture. We interrogated a microarray data set from a second cohort of 29 patients and compared the TMEs of ARID1A-wildtype (ARID1Awt) versus ARID1A-mutant (ARID1Amut) disease. We found significant variations in immune cell frequency and phenotype, checkpoint expression, and collagen matrix between the malignant cell area (MCA), leading edge (LE), and stroma. The MCA had the largest population of CD138+ plasma cells, the LE had more CD20+ B cells and T cells, whereas the stroma had more mast cells and αSMA+ fibroblasts. PD-L2 was expressed predominantly on malignant cells and was the dominant PD-1 ligand. Compared with early CCOC, advanced-stage disease had significantly more fibroblasts and a more complex collagen matrix, with microarray analysis indicating "TGFβ remodeling of the extracellular matrix" as the most significantly enriched pathway. Data showed significant differences in immune cell populations, collagen matrix, and cytokine expression between ARID1Awt and ARID1Amut CCOC, which may reflect different paths of tumorigenesis and the relationship to endometriosis. Increased infiltration of CD8+ T cells within the MCA and CD4+ T cells at the LE and stroma significantly associated with decreased overall survival.

Indexed as

Ovarian NeoplasmsTumor MicroenvironmentCD8-Positive T-LymphocytesCollagenFemaleHumansProgrammed Cell Death 1 ReceptorCollagenProgrammed Cell Death 1 Receptor

Identifiers

PMID36095166
PMCPMC9627265
OpenAlexW4295309178

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.