Evidence map›Paper›PMID 37040900›Full record

ArticleHistopathology2023

High mesothelin expression by immunohistochemistry predicts improved survival in pleural mesothelioma.

Gerard J Chu, Anthony Linton, Steven Kao, Sonja Klebe, Stephen Adelstein, Dannel Yeo, John E J Rasko, Wendy A Cooper

Open access · hybridAbstract read
In one paragraph

Article in Histopathology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

10 citing papers in PubMed, 13 citations in OpenAlex.

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  7. Regional and intratumoral adoptive T-cell therapy.Immuno-oncology technology · 2024
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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

8 authors at 2 institutions in 2 countries.

Gerard J ChuGene and Stem Cell Therapy Program Centenary Institute, University of Sydney, Sydney, NSW, Australia.ORCID https://orcid.org/0000-0001-9033-4554
Anthony LintonFaculty of Medicine and Health, University of Sydney, Sydney, NSW, Australia.
Steven KaoFaculty of Medicine and Health, University of Sydney, Sydney, NSW, Australia.
Sonja KlebeAsbestos Diseases Research Institute, Concord, NSW, Australia.
Stephen AdelsteinDepartment of Clinical Immunology and Allergy, Royal Prince Alfred Hospital, Camperdown, NSW, Australia.
Dannel YeoGene and Stem Cell Therapy Program Centenary Institute, University of Sydney, Sydney, NSW, Australia.
John E J RaskoGene and Stem Cell Therapy Program Centenary Institute, University of Sydney, Sydney, NSW, Australia.
Wendy A CooperFaculty of Medicine and Health, University of Sydney, Sydney, NSW, Australia.ORCID https://orcid.org/0000-0001-5418-4229
The University of Sydney · AUSouth Australia Pathology · AU

Funding

Cancer Council of NSW PW18-030Cancer Council of NSW RG20-07CSR LtdLi Ka Shing FoundationNational Health and Medical Research Council 1177305National Health and Medical Research Council APP1169460Royal College of Pathologists of AustralasiaSydney Local Health District
6 · The paper itself

Abstract

aimsMesothelin (MSLN) is a cancer-associated antigen that is overexpressed in malignancies such as mesothelioma, pancreatic and ovarian cancer. It is also a target for novel personalised therapies, including antibodies, antibody-drug conjugates and chimeric antigen receptor T cells. Immunohistochemistry may predict those who would best respond to anti-mesothelin therapies and guide decisions in therapeutic strategy. This study aimed to assess the intensity and distribution of MSLN immunostaining in mesothelioma, and to determine the prognostic value of MSLN expression by histochemical-score (H-score). METHODS AND

resultsThe MN1 anti-MSLN antibody was used to stain a formalin-fixed paraffin-embedded tissue microarray of histologically confirmed mesothelioma from 75 consecutive patients who had undergone pleurectomy with or without decortication. MSLN positivity, the staining intensity, distribution of staining and H-score were evaluated. The correlation of H-score with prognosis was investigated. Sixty-six per cent of epithelioid tumours were MSLN-positive (with expression in > 5% tumour cells). Of MSLN-expressing epithelioid tumours, 70.4% had moderate (2+) or strong (3+) intensity MSLN immunostaining, although only 37% of samples had staining in ≥ 50% of tumour cells. In multivariate analysis, MSLN H-score as a continuous variable and an H-score ≥ 33 were independent predictors of improved survival (P = 0.04 and P < 0.001, respectively).

conclusionsMSLN expression was more heterogenous in epithelioid mesothelioma than reported previously. Therefore, it would be appropriate to perform an immunohistochemical assessment of MSLN expression to stratify and assess patient suitability for mesothelin-targeted personalised therapies, such as chimeric antigen receptor T cells.

Indexed as

MesotheliomaMesothelioma, MalignantPleural NeoplasmsReceptors, Chimeric AntigenGPI-Linked ProteinsHumansImmunohistochemistryMesothelinGPI-Linked ProteinsMesothelinMSLN protein, humanReceptors, Chimeric Antigenantibodieschimeric antigen receptor T cellsepithelioidexpressionimmunohistochemistrymesothelinmesotheliomaprognosis

Identifiers

PMID37040900
PMCPMC10952516
OpenAlexW4364356450

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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.