Evidence map›Paper›PMID 30209885›Full record

ArticleThoracic cancer2018

Comparable immunoreactivity rates of PD-L1 in archival and recent specimens from non-small cell lung cancer.

Yuki Nakamura, Tetsu Kobayashi, Yoichi Nishii, Yuta Suzuki, Haruko Saiki, Kentaro Ito, Fumiaki Watanabe, Kota Nishihama, Taro Yasuma, Corina N D'Alessandro-Gabazza and 5 more

Open access · goldAbstract read
In one paragraph

Article in Thoracic cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
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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

15 authors at 2 institutions in 1 country.

Yuki NakamuraRespiratory Center, Matsusaka Municipal Hospital, Matsusaka, Japan.
Tetsu KobayashiDepartment of Pulmonary and Critical Care Medicine, Mie University Faculty and Graduate School of Medicine, Tsu, Japan.
Yoichi NishiiRespiratory Center, Matsusaka Municipal Hospital, Matsusaka, Japan.
Yuta SuzukiRespiratory Center, Matsusaka Municipal Hospital, Matsusaka, Japan.
Haruko SaikiRespiratory Center, Matsusaka Municipal Hospital, Matsusaka, Japan.
Kentaro ItoRespiratory Center, Matsusaka Municipal Hospital, Matsusaka, Japan.
Fumiaki WatanabeRespiratory Center, Matsusaka Municipal Hospital, Matsusaka, Japan.
Kota NishihamaDepartment of Immunology, Mie University Faculty and Graduate School of Medicine, Tsu, Japan.
Taro YasumaDepartment of Immunology, Mie University Faculty and Graduate School of Medicine, Tsu, Japan.
Corina N D'Alessandro-GabazzaDepartment of Immunology, Mie University Faculty and Graduate School of Medicine, Tsu, Japan.
Koji KatsutaDepartment of Pathology, Matsusaka Municipal Hospital, Matsusaka, Japan.
Hajime FujimotoDepartment of Pulmonary and Critical Care Medicine, Mie University Faculty and Graduate School of Medicine, Tsu, Japan.
Esteban C GabazzaDepartment of Immunology, Mie University Faculty and Graduate School of Medicine, Tsu, Japan.ORCID 0000-0003-2536-898X
Osamu TaguchiCenter for Mental and Physical Health, Mie University, Tsu, Japan.
Osamu HatajiRespiratory Center, Matsusaka Municipal Hospital, Matsusaka, Japan.
Soka Municipal Hospital · JPMie University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMolecular targeted therapy including the use of monoclonal antibodies directed against the immune checkpoints PD-L1 and PD-1 receptor have remarkably improved the therapeutic response and survival of cancer patients. The tumor expression level of PD-L1 can predict the response rate to checkpoint inhibitors. We evaluated whether the time interval between tumor tissue sampling/paraffinization and immunohistochemistry affects the staining level of PD-L1 in non-small cell lung cancer (NSCLC).

methodsThis study comprised 137 patients with NSCLC. Tumors were stained with 22C3 or 28-8 antibodies.

resultsThere was a significant correlation between the immunoreactivity rate of tumor tissues obtained using 22C3 and 28-8 clones. No statistical difference in immunoreactivity between archival and recent samples stained either with 22C3 or 28-8 antibodies was observed. The immunoreactivity rate achieved with 22C3 or 28-8 antibodies significantly correlated with tumor histological type and size, but not with specimen storage time, age, gender, smoking history, clinical stage, or lymph node metastasis.

conclusionIn brief, the results of this study show that the time interval between tissue sampling/paraffinization and immunohistochemical analysis has no influence on the immunoreactivity rate of PD-L1 in NSCLC.

Indexed as

AgedB7-H1 AntigenBiomarkers, TumorCarcinoma, Non-Small-Cell LungFemaleHumansLung NeoplasmsMaleB7-H1 AntigenBiomarkers, TumorCD274 protein, humanArchival specimenimmune checkpoint inhibitormolecular targeted therapynon-small cell lung cancerPD-L1

Identifiers

PMID30209885
PMCPMC6209791
OpenAlexW2892146265

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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.