Evidence map›Paper›PMID 34811933›Full record

ArticleThoracic cancer2022

Solid histological component of adenocarcinoma might play an important role in PD-L1 expression of lung adenocarcinoma.

Tomoyuki Miyazawa, Kei Morikawa, Kanji Otsubo, Hiroki Sakai, Hiroyuki Kimura, Motohiro Chosokabe, Naoki Furuya, Hideki Marushima, Koji Kojima, Masamichi Mineshita and 2 more

Open access · goldAbstract read
In one paragraph

Article in Thoracic cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.6field-weighted citation impact, top 28% 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

8 citing papers in PubMed, 7 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

12 authors at 1 institution in 1 country.

Tomoyuki MiyazawaDepartment of Chest Surgery, St. Marianna University School of Medicine, Kawasaki, Japan.ORCID 0000-0001-6634-8200
Kei MorikawaDivision of Respiratory Medicine, Department of Internal Medicine, St. Marianna University School of Medicine, Kawasaki, Japan.ORCID 0000-0002-0745-5118
Kanji OtsuboDepartment of Chest Surgery, St. Marianna University School of Medicine, Kawasaki, Japan.ORCID 0000-0003-4978-4988
Hiroki SakaiDepartment of Chest Surgery, St. Marianna University School of Medicine, Kawasaki, Japan.
Hiroyuki KimuraDepartment of Chest Surgery, St. Marianna University School of Medicine, Kawasaki, Japan.
Motohiro ChosokabeDepartment of Pathology, St. Marianna University School of Medicine, Kawasaki, Japan.
Naoki FuruyaDivision of Respiratory Medicine, Department of Internal Medicine, St. Marianna University School of Medicine, Kawasaki, Japan.ORCID 0000-0001-7162-5946
Hideki MarushimaDepartment of Chest Surgery, St. Marianna University School of Medicine, Kawasaki, Japan.
Koji KojimaDepartment of Chest Surgery, St. Marianna University School of Medicine, Kawasaki, Japan.
Masamichi MineshitaDivision of Respiratory Medicine, Department of Internal Medicine, St. Marianna University School of Medicine, Kawasaki, Japan.ORCID 0000-0002-6933-6579
Junki KoikeDepartment of Pathology, St. Marianna University School of Medicine, Kawasaki, Japan.
Hisashi SajiDepartment of Chest Surgery, St. Marianna University School of Medicine, Kawasaki, Japan.ORCID 0000-0003-3490-7658
St. Marianna University School of Medicine · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn this study we aimed to clarify the PD-L1 positive expression in lung adenocarcinoma, including various adenocarcinoma subtypes paying particular attention to its component.

methodsA total of 307 lung adenocarcinoma patients who underwent lobectomy or segmentectomy, as well as systematic lymph node dissection (ND2a), from February 2008 to March 2020 at our hospital, were enrolled into the study. A final diagnosis of adenocarcinoma was obtained from the resected lung specimens of all 307 patients to determine the histological type, adenocarcinoma subtype, and component of adenocarcinoma by ethics of 5%. PD-L1 was immunohistochemically stained using the murine monoclonal antibody clone 22C3.

resultsWhen PD-L1 expression-positive was defined by tumor proportion score (TPS) ≥1%, the positive cases were 6/33 in adenocarcinoma (Ad) in situ (AIS), 2/26 in minimally invasive Ad (MIA), 12/60 in lepidic predominant Ad (LPA), 44/91 in papillary predominant Ad (PPA), 24/49 in acinar predominant Ad (APA), 23/28 in solid predominant Ad (SPA), 4/7 in micropapillary predominant Ad (MPA), and 0/13 in invasive mucinous Ad (IMA). In the high proportion group (APA, PPA, SPA, and MPA) of PD-L1 expression, SPA was the only subtype which was statistically significant when both PD-L1 expression-positive was defined by TPS ≥ 1% (p < 0.0001) and TPS ≧ 50% (p < 0.0001). We then considered the solid component. We investigated 279 cases of the other subtype group excluding SPA. The group containing a solid component (≥5%) tended to be PD-L1 expression-positive both when defined by TPS ≥1% (p < 0.0001) and TPS ≧50% (p = 0.0049).

conclusionsThe PD-L1 expression tended to be positive when a solid component was confirmed (≥5%) in specimens of lung adenocarcinoma patients.

Indexed as

Adenocarcinoma of LungAdultAgedAged, 80 and overB7-H1 AntigenBiomarkers, TumorFemaleHumansLung NeoplasmsMaleMiddle AgedB7-H1 AntigenBiomarkers, TumorCD274 protein, humanearly adenocarcinomaimmunohistochemistrylung cancerPD-L1subtype

Identifiers

PMID34811933
PMCPMC8720631
OpenAlexW3216802697

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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.