Evidence map›Paper›PMID 36519023›Full record

ArticleTranslational lung cancer research2022

Immune profile analysis of peripheral blood and tumors of lung cancer patients treated with immune checkpoint inhibitors.

Yoshinobu Ichiki, Takashi Fukuyama, Mari Ueno, Yoshiro Kanasaki, Hidenori Goto, Mai Takahashi, Shuji Mikami, Noritada Kobayashi, Kozo Nakanishi, Shinichi Hayashi and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Translational lung cancer research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

11 citing papers in PubMed, 11 citations in OpenAlex.

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  11. Dynamic change of CD8Translational lung cancer research · 2023
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 1 country.

Yoshinobu IchikiDepartment of General Thoracic Surgery, National Hospital Organization, Saitama Hospital, Wako, Japan.
Takashi FukuyamaDivision of Biomedical Research, Kitasato University Medical Center, Kitamoto, Japan.
Mari UenoDepartment of Diagnostic Pathology, National Hospital Organization, Saitama Hospital, Wako, Japan.
Yoshiro KanasakiDepartment of General Thoracic Surgery, National Hospital Organization, Saitama Hospital, Wako, Japan.
Hidenori GotoDepartment of General Thoracic Surgery, National Hospital Organization, Saitama Hospital, Wako, Japan.
Mai TakahashiDepartment of Respiratory Medicine, National Hospital Organization, Saitama Hospital, Wako, Japan.
Shuji MikamiDepartment of Diagnostic Pathology, National Hospital Organization, Saitama Hospital, Wako, Japan.
Noritada KobayashiDivision of Biomedical Research, Kitasato University Medical Center, Kitamoto, Japan.
Kozo NakanishiDepartment of General Thoracic Surgery, National Hospital Organization, Saitama Hospital, Wako, Japan.
Shinichi HayashiDepartment of Respiratory Medicine, National Hospital Organization, Saitama Hospital, Wako, Japan.
Tsuyoshi IshidaDepartment of Diagnostic Pathology, National Hospital Organization, Saitama Hospital, Wako, Japan.
National Hospital Organization · JPKitasato University Medical Center · JPUniversity of Occupational and Environmental Health Japan · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Immune checkpoint inhibitors (ICIs) have become central to lung cancer drug therapy, and establishing biomarkers that can predict effects and adverse events (AEs) is awaited. We prospectively analyzed the association between the immune-related molecular expression in peripheral blood mononuclear cells (PBMCs) and lung cancer tissues, and the effects of ICI monotherapy. Methods: Twenty-one patients with advanced non-small cell lung cancer (NSCLC) who received ICI monotherapy were included. Changes in the expression of immune-related molecules in PBMCs before and after the administration of ICI were analyzed by flow cytometry. The major histocompatibility complex (MHC) class I and programmed cell death-ligand 1 (PD-L1) expression of cancer cells, and the PD-L1, CD8 and CD103 expression of tumor infiltrating immune cells in lung cancer tissue before the administration of ICI were confirmed by immunohistochemistry (IHC). Results: Twenty-one patients were investigated, including 11 adenocarcinoma and 10 squamous cell carcinoma cases. Anti-programmed cell death protein-1 (PD-1) antibody (n=18) and anti-PD-L1 antibody (n=3) were administered. The clinical responses were graded as follows: complete response (CR) (n=1), partial response (PR) (n=7), stable disease (SD) (n=10) and progressive disease (PD) (n=3). Among immune-related molecules expressed in PBMCs, the CD103 Conclusions: The CD103

Indexed as

CD103immune checkpoint inhibitor (ICI)Lung cancerPD-1tumor immunology

Identifiers

PMID36519023
PMCPMC9742629
OpenAlexW4311820913

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.