Evidence map›Paper›PMID 32445029›Full record

ArticleCancer immunology, immunotherapy : CII2020

Expression of programmed death-ligand 1 (PD-L1) in human pituitary neuroendocrine tumor.

Valentine Suteau, Alexandre Collin, Philippe Menei, Patrice Rodien, Marie-Christine Rousselet, Claire Briet

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

16 citing papers in PubMed, 24 citations in OpenAlex.

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  9. Tumour microenvironment and pituitary tumour behaviour.Journal of endocrinological investigation · 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

6 authors at 2 institutions in 1 country.

Valentine SuteauLaboratoire MITOVASC, UMR CNRS 6015, INSERM 1083, University of Angers, Angers, France.
Alexandre CollinDépartement de Pathologie Cellulaire et Tissulaire, CHU Angers, Angers, France.
Philippe MeneiDépartement de Neurochirurgie, CHU Angers, Angers, France.
Patrice RodienLaboratoire MITOVASC, UMR CNRS 6015, INSERM 1083, University of Angers, Angers, France.
Marie-Christine RousseletDépartement de Pathologie Cellulaire et Tissulaire, CHU Angers, Angers, France.
Claire BrietLaboratoire MITOVASC, UMR CNRS 6015, INSERM 1083, University of Angers, Angers, France. claire.briet@chu-angers.fr.ORCID http://orcid.org/0000-0003-1250-345X
Centre Hospitalier Universitaire d'Angers · FRCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo explore the programmed death-ligand 1 (PD-L1) expression in varied subtypes of pituitary neuroendocrine tumors with assessment of their clinical behavior at diagnosis and follow-up.

methodsWe conducted a retrospective monocentric study, including all patients operated in the Academic Hospital of Angers (France) for a pituitary neuroendocrine tumor between 2012 and 2018. PDL-1 immunostaining was performed using a European Conformity-In Vitro Diagnostic-labeled anti-PDL1 antibody (clone 22C3). PD-L1 immunostaining was evaluated as the percentage of tumor cells showing positive membrane staining, into four grades: grade 0 = < 1%, grade 1 = 1 to 5%, grade 2 = 6 to 49% and grade 3 = ≥ 50%. PD-L1 expression was compared with tumor features (secretion, proliferation, invasion) and outcome.

resultsThe study included 139 pituitary neuroendocrine tumors, including 84 (60%) nonfunctioning adenomas. Twenty-five pituitary neuroendocrine tumors were PD-L1 positive (18%), including 3 grade 3, 8 grade 2 and 14 grade 1. PD-L1 expression was not different between functioning and nonfunctioning adenomas (p = 0.26). Among 16 tumors with proliferative markers (Ki-67 ≥ 3% and p53 positive), only one was PD-L1 positive.

conclusionIn our series, PD-L1 was expressed in a rather small proportion of PitNET (18%), and this immune marker was not associated with any biological characteristic or behavior of the pituitary tumors. Thus, PD-L1 staining may be necessary before considering PD-L1 blockage in pituitary neuroendocrine tumors, in case of therapeutic impasse.

Indexed as

B7-H1 AntigenBiomarkers, TumorFemaleFollow-Up StudiesHumansMaleMiddle AgedNeoplasm Recurrence, LocalNeuroendocrine TumorsPituitary NeoplasmsPrognosisRetrospective StudiesSurvival RateB7-H1 AntigenBiomarkers, TumorCD274 protein, humanClone 22C3ImmunohistochemistryImmunotherapyPD-L1Pituitary neuroendocrine tumor

Identifiers

PMID32445029
PMCPMC11027687
OpenAlexW3027454003

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.