Evidence map›Paper›PMID 37208929›Full record

ArticleThoracic cancer2023

Prognostic and predictive value of CD163 expression and the CD163/CD68 expression ratio for response to adjuvant chemotherapy in patients with surgically resected lung squamous cell carcinoma.

Naoki Yanagawa, Shunsuke Shikanai, Mayu Sugai, Yoshihiko Koike, Yoshinari Asai, Takayuki Tanji, Ryo Sugimoto, Mitsumasa Osakabe, Noriyuki Uesugi, Hajime Saito and 2 more

Open access · goldAbstract read
In one paragraph

Article in Thoracic cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

10 citing papers in PubMed, 9 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.

Naoki YanagawaDepartment of Molecular Diagnostic Pathology, Iwate Medical University, Yahaba-cho, Japan.ORCID 0000-0002-0818-7151
Shunsuke ShikanaiDepartment of Molecular Diagnostic Pathology, Iwate Medical University, Yahaba-cho, Japan.
Mayu SugaiDepartment of Molecular Diagnostic Pathology, Iwate Medical University, Yahaba-cho, Japan.
Yoshihiko KoikeDepartment of Molecular Diagnostic Pathology, Iwate Medical University, Yahaba-cho, Japan.
Yoshinari AsaiDepartment of Molecular Diagnostic Pathology, Iwate Medical University, Yahaba-cho, Japan.
Takayuki TanjiDepartment of Molecular Diagnostic Pathology, Iwate Medical University, Yahaba-cho, Japan.
Ryo SugimotoDepartment of Molecular Diagnostic Pathology, Iwate Medical University, Yahaba-cho, Japan.
Mitsumasa OsakabeDepartment of Molecular Diagnostic Pathology, Iwate Medical University, Yahaba-cho, Japan.
Noriyuki UesugiDepartment of Molecular Diagnostic Pathology, Iwate Medical University, Yahaba-cho, Japan.
Hajime SaitoDepartment of Thoracic Surgery, Iwate Medical University, Yahaba-cho, Japan.ORCID 0000-0003-0912-1637
Makoto MaemondoDivision of Pulmonary Medicine, Department of Internal Medicine, Iwate Medical University, Yahaba-cho, Japan.
Tamotsu SugaiDepartment of Molecular Diagnostic Pathology, Iwate Medical University, Yahaba-cho, Japan.
Iwate Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMacrophages infiltrating the tumor microenvironment are defined as tumor-associated macrophages (TAMs). TAMs can be polarized into different phenotypes, that is, proinflammatory M1 macrophages or anti-inflammatory M2 macrophages. Particularly, M2 macrophages promote angiogenesis, wound healing, and tumor growth. This study aimed to evaluate whether M2 TAMs can serve as a useful marker to predict prognosis and benefit from adjuvant chemotherapy in patients with surgically resected lung squamous cell carcinomas (SCCs).

methodsWe examined 104 patients with SCC. Tissue microarrays were constructed, and the density of TAMs was analyzed by immunohistochemistry for expression of CD68 and CD163. The relationship between CD68 and CD163 expression and the CD163/CD68 expression rate and clinicopathological characteristics including patient outcomes were investigated. In addition, propensity score matching (PSM) analysis was conducted to test the hypothesis that these cells significantly influenced chemotherapy responses.

resultsUnivariate analysis revealed that pathological stage, CD163 expression, and the CD163/CD68 expression ratio were significant prognostic factors. Multivariate analysis showed that these factors were all independent prognostic factors. Thirty-four pairs were determined by using PSM analysis. Patients with a low CD163/CD68 expression ratio benefited more from adjuvant chemotherapy than those with a high ratio.

conclusionWe suggest that M2 TAMs may be a useful marker to predict prognosis and differential benefit from adjuvant chemotherapy in patients with surgically resected lung SCCs.

Indexed as

Carcinoma, Non-Small-Cell LungCarcinoma, Squamous CellLung NeoplasmsCD163 AntigenChemotherapy, AdjuvantHumansLungPrognosisTumor MicroenvironmentCD163 Antigenchemotherapylung squamous cell carcinomaprognosistumor-associated macrophage (TAM)

Identifiers

PMID37208929
PMCPMC10344737
OpenAlexW4377137865

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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.