Evidence map›Paper›PMID 34584854›Full record

ArticleTranslational lung cancer research2021

An analysis of the immunological tumor microenvironment of primary tumors and regional lymph nodes in squamous cell lung cancer.

Yoshinobu Ichiki, Mari Ueno, Shinya Yanagi, Yoshiro Kanasaki, Hidenori Goto, Takashi Fukuyama, Shuji Mikami, Kozo Nakanishi, Tsuyoshi Ishida

Open access · diamondAbstract read
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Article in Translational lung cancer research, 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
0.4field-weighted citation impact, top 37% 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, 5 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

9 authors at 3 institutions in 1 country.

Yoshinobu IchikiDepartment of General Thoracic Surgery, National Hospital Organization, Saitama Hospital, Wako, Japan.
Mari UenoDepartment of Diagnostic Pathology, National Hospital Organization, Saitama Hospital, Wako, Japan.
Shinya YanagiDepartment 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.
Takashi FukuyamaDivision of Biomedical Research, Kitasato University Medical Center, Kitamoto, Japan.
Shuji MikamiDepartment of Diagnostic Pathology, National Hospital Organization, Saitama Hospital, Wako, Japan.
Kozo NakanishiDepartment of General Thoracic Surgery, 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

backgroundVarious immune cells that play a central role in antitumor immunity accumulate in primary tumors and regional lymph nodes. Such cellular accumulation and the molecular expression were analyzed to elucidate the immunological tumor microenvironment.

methodsFifty squamous cell lung cancer patients with complete resection were included. Resected specimens from primary lung tumors and regional lymph nodes were immunostained for immune-related molecules, such as CD8, CD103, major histocompatibility complex (MHC) class I, and programmed cell death protein ligand-1 (PD-L1), and the relationship between the prognosis and clinicopathological factors was retrospectively analyzed.

resultsTumor-infiltrating lymphocytes and CD8+ lymphocytes, intratumoral and intrastromal CD103+ lymphocytes, tumor diameter, pathological T and N factors, and pathological stage were significant prognostic factors for the disease-specific survival (DSS) in a univariate analysis. In a multivariate analysis, intratumoral and intrastromal CD103+ lymphocytes and pathological T and N factors were independent prognostic factors of the DSS. Significant concordance was found between the PD-L1 expression of primary tumors and metastatic lymph nodes as well as among tumor-infiltrating lymphocytes, CD8+ lymphocytes and CD103+ lymphocytes. Infiltration of CD103+ lymphocytes into the tumor was significantly correlated with an increased PD-L1 expression of cancer cells in both primary tumors and reginal lymph node metastases. Both the intratumoral infiltration of CD103+ lymphocytes and PD-L1 expression of cancer cells were significantly higher in lymph node metastases than in primary tumors.

conclusionsCD103+ lymphocyte infiltration in the primary tumor was shown to be strongly involved in the prognosis.

Indexed as

CD103CTLLung cancerprogrammed cell death protein ligand-1 (PD-L1)tumor immunology

Identifiers

PMID34584854
PMCPMC8435388
OpenAlexW3195537958

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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.