Evidence map›Paper›PMID 33772818›Full record

ArticleHistopathology2021

False-negative programmed death-ligand 1 immunostaining in ethanol-fixed endobronchial ultrasound-guided transbronchial needle aspiration specimens of non-small-cell lung cancer patients.

Bregje M Koomen, Willem Vreuls, Mirthe de Boer, Emma J de Ruiter, Juergen Hoelters, Aryan Vink, Stefan M Willems

Open access · hybridAbstract read
In one paragraph

Article in Histopathology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

5 citing papers in PubMed, 11 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

7 authors at 3 institutions in 1 country.

Bregje M KoomenDepartment of Pathology, University Medical Centre Utrecht, Utrecht University, Utrecht, the Netherlands.ORCID https://orcid.org/0000-0002-3106-5734
Willem VreulsDepartment of Pathology, Canisius-Wilhelmina Hospital, Nijmegen, the Netherlands.
Mirthe de BoerDepartment of Pathology, University Medical Centre Utrecht, Utrecht University, Utrecht, the Netherlands.
Emma J de RuiterDepartment of Pathology, University Medical Centre Utrecht, Utrecht University, Utrecht, the Netherlands.
Juergen HoeltersDepartment of Pulmonology, Canisius-Wilhelmina Hospital, Nijmegen, the Netherlands.
Aryan VinkDepartment of Pathology, University Medical Centre Utrecht, Utrecht University, Utrecht, the Netherlands.
Stefan M WillemsDepartment of Pathology, University Medical Centre Utrecht, Utrecht University, Utrecht, the Netherlands.
Utrecht University · NLCanisius-Wilhelmina Ziekenhuis · NLUniversity Medical Center Groningen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsProgrammed death-ligand 1 (PD-L1) immunostaining is used to predict which non-small-cell lung cancer (NSCLC) patients will respond best to treatment with programmed cell death protein 1/PD-L1 inhibitors. PD-L1 immunostaining is sometimes performed on alcohol-fixed cytological specimens instead of on formalin-fixed paraffin-embedded (FFPE) biopsies or resections. We studied whether ethanol prefixation of clots from endobronchial ultrasound-guided transbronchial needle aspiration (EBUS-TBNA) results in diminished PD-L1 immunostaining as compared with formalin fixation. METHODS AND

resultsFFPE cell blocks from EBUS-TBNA specimens of 54 NSCLC patients were identified. For each case, paired samples were available, consisting of clots directly immersed in formalin and clots prefixed in Fixcyt (50% ethanol). Serial sections were immunostained for PD-L1 by use of the standardised SP263 assay and the 22C3 antibody as a laboratory-developed test (LDT). PD-L1 positivity was determined with two cut-offs (1% and 50%). Concordance of PD-L1 positivity between the formalin-fixed (gold standard) and ethanol-prefixed material was assessed. When the 22C3 LDT was used, 30% and 36% of the ethanol-prefixed specimens showed false-negative results at the 1% and 50% cut-offs, respectively (kappa 0.64 and 0.68). When SP263 was used, 22% of the ethanol-prefixed specimens showed false-negative results at the 1% cut-off (kappa 0.67). At the 50% cut-off, concordance was higher (kappa 0.91), with 12% of the ethanol-prefixed specimens showing false-negative results.

conclusionEthanol fixation of EBUS-TBNA specimens prior to formalin fixation can result in a considerable number of false-negative PD-L1 immunostaining results when a 1% cut-off is used and immunostaining is performed with SP263 or the 22C3 LDT. The same applies to use of the 50% cut-off when immunostaining is performed with the 22C3 LDT.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsB7-H1 AntigenBiomarkers, TumorEndoscopic Ultrasound-Guided Fine Needle AspirationEthanolFalse Negative ReactionsHumansImmunohistochemistryOrgan Preservation SolutionsTissue FixationB7-H1 AntigenBiomarkers, TumorCD274 protein, humanEthanolOrgan Preservation Solutions22C3 antibodycytologyimmunohistochemistryimmunotherapynon-small-cell lung carcinomaprogrammed cell death-ligand 1SP263 antibodytissue fixation

Identifiers

PMID33772818
PMCPMC8519150
OpenAlexW3146879004

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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.