Evidence map›Paper›PMID 34128367›Full record

ArticleJournal of breast cancer2021

Programmed Death Ligand 1 Immunohistochemistry in Triple-Negative Breast Cancer: Evaluation of Inter-Pathologist Concordance and Inter-Assay Variability.

Soomin Ahn, Ji Won Woo, Hyojin Kim, Eun Yoon Cho, Ahrong Kim, Jee Yeon Kim, Chungyeul Kim, Hee Jin Lee, Ji Shin Lee, Young Kyung Bae and 3 more

Open access · goldAbstract read
In one paragraph

Article in Journal of breast cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.5field-weighted citation impact, top 14% 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

13 citing papers in PubMed, 20 citations in OpenAlex.

  1. Clinical Outcomes and Immune Markers by Race in a Phase I/II Clinical Trial of Durvalumab Concomitant with Neoadjuvant Chemotherapy in Early-Stage TNBC.Clinical cancer research : an official journal of the American Association for Cancer Research · 2022
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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

13 authors at 9 institutions in 1 country.

Soomin AhnDepartment of Pathology, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam, Korea.ORCID https://orcid.org/0000-0002-1979-4010
Ji Won WooDepartment of Pathology, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam, Korea.ORCID https://orcid.org/0000-0003-1659-7123
Hyojin KimDepartment of Pathology, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam, Korea.ORCID https://orcid.org/0000-0001-9201-8328
Eun Yoon ChoDepartment of Pathology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0001-5849-3600
Ahrong KimDepartment of Pathology, School of Medicine, Pusan National University, Busan, Korea.ORCID https://orcid.org/0000-0003-2317-8920
Jee Yeon KimDepartment of Pathology, School of Medicine, Pusan National University, Busan, Korea.ORCID https://orcid.org/0000-0002-0503-984X
Chungyeul KimDepartment of Pathology, College of Medicine, Korea University, Seoul, Korea.ORCID https://orcid.org/0000-0002-9636-5228
Hee Jin LeeDepartment of Pathology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Korea.ORCID https://orcid.org/0000-0002-4963-6603
Ji Shin LeeDepartment of Pathology, Chonnam National University Medical School, Gwangju, Korea.ORCID https://orcid.org/0000-0003-4634-2228
Young Kyung BaeDepartment of Pathology, Yeungnam University College of Medicine, Daegu, Korea.ORCID https://orcid.org/0000-0002-6689-9413
Youngmee KwonDepartment of Pathology, National Cancer Center, Goyang, Korea.ORCID https://orcid.org/0000-0002-1370-2496
Wan Seop KimDepartment of Pathology, Konkuk University School of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0001-7704-5942
So Yeon ParkDepartment of Pathology, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam, Korea. sypmd@snu.ac.kr.ORCID https://orcid.org/0000-0002-0299-7268
Seoul National University Bundang Hospital · KRPusan National University · KRSamsung Medical Center · KRChonnam National University Hospital · KRKonkuk University · KRKorea University · KRNational Cancer Center · KRUlsan College · KRYeungnam University College

Funding

National Research Foundation of Korea NRF-2018R1A2B6005559Seoul National University
6 · The paper itself

Abstract

purposeThe programmed death ligand 1 (PD-L1) SP142 assay with a 1% immune cell (IC) cutoff is approved for the selection of advanced triple-negative breast cancer (TNBC) patients for atezolizumab treatment. We aimed to evaluate the interobserver concordance of PD-L1 scoring and inter-assay variability of various PD-L1 assays in TNBC.

methodsThirty patients with primary TNBC were selected, and SP142, SP263, 22C3, and E1L3N assays were performed. PD-L1 staining in ICs and tumor cells (TCs) was scored by 10 pathologists who were blinded to the assay. The interobserver concordance among pathologists and the inter-assay variability of the four PD-L1 assays were analyzed. For SP142, the intraobserver concordance among the six pathologists was analyzed after training.

resultsThe adjusted means of PD-L1 IC scoring ranged from 6.2% to 12.9% for the four assays; the intraclass correlations showed moderate (0.584-0.649) reader concordance. The PD-L1 IC scoring with a 1% cutoff resulted in identical scoring in 40.0%-66.7% of cases and a poor to moderate agreement (Fleiss κ statistic [FKS] = 0.345-0.534) for the four assays. The SP142 assay had the widest range of positive rate (56.5%-100.0%), lowest number of cases with identical scoring, and lowest FKS at 1% cutoff. Pairwise comparison of adjusted means showed significantly decreased PD-L1 staining in SP142 compared with the other assays in both ICs and TCs. As for the intraobserver concordance in the SP142 assay, the overall percent agreement was 87.8% with a 1% IC cutoff. After training, the proportion of cases with identical scoring at a 1% IC cutoff increased to 70.0%; the FKS also increased to 0.610.

conclusionThe concordance of PD-L1 IC scoring among pathologists was low, at the 1% cutoff for the SP142 assay without training. SP142 showed the lowest PD-L1 expression in both IC and TC.

Indexed as

B7-H1 antigenImmune checkpoint inhibitorsImmunohistochemistryObserver variationTriple negative breast cancer

Identifiers

PMID34128367
PMCPMC8250096
OpenAlexW3169461145

What OpenQuestion holds

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LicenceCC BY-NC
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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.