Evidence map›Paper›PMID 33262828›Full record

ArticleOncology letters2021

CD204-positive macrophages accumulate in breast cancer tumors with high levels of infiltrating lymphocytes and programmed death ligand-1 expression.

Mayuko Nagano, Kanako Saito, Yuji Kozuka, Masako Ichishi, Hiroto Yuasa, Aya Noro, Nao Imai, Mai Shibusawa, Mao Kimoto, Makoto Ishitobi and 6 more

Open access · diamondAbstract read
In one paragraph

Article in Oncology letters, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

9 citing papers in PubMed, 11 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

16 authors at 2 institutions in 1 country.

Mayuko NaganoDepartment of Breast Surgery, Mie University Graduate School of Medicine, Mie 514-8507, Japan.
Kanako SaitoDepartment of Hematology and Oncology, Mie University Graduate School of Medicine, Mie 514-8507, Japan.
Yuji KozukaDepartment of Pathology, Mie University Hospital, Mie 514-8507, Japan.
Masako IchishiDepartment of Pathology, Mie University Hospital, Mie 514-8507, Japan.
Hiroto YuasaDepartment of Pathology, Mie University Hospital, Mie 514-8507, Japan.
Aya NoroDepartment of Breast Surgery, Mie University Graduate School of Medicine, Mie 514-8507, Japan.
Nao ImaiDepartment of Breast Surgery, Mie University Graduate School of Medicine, Mie 514-8507, Japan.
Mai ShibusawaDepartment of Breast Surgery, Mie University Graduate School of Medicine, Mie 514-8507, Japan.
Mao KimotoDepartment of Breast Surgery, Mie University Graduate School of Medicine, Mie 514-8507, Japan.
Makoto IshitobiDepartment of Breast Surgery, Mie University Graduate School of Medicine, Mie 514-8507, Japan.
Yasutaka TonoDepartment of Hematology and Oncology, Mie University Graduate School of Medicine, Mie 514-8507, Japan.
Hiroyasu OdaDepartment of Hematology and Oncology, Mie University Graduate School of Medicine, Mie 514-8507, Japan.
Mikiya IshiharaDepartment of Hematology and Oncology, Mie University Graduate School of Medicine, Mie 514-8507, Japan.
Toshiro MizunoDepartment of Hematology and Oncology, Mie University Graduate School of Medicine, Mie 514-8507, Japan.
Tomoko OgawaDepartment of Breast Surgery, Mie University Graduate School of Medicine, Mie 514-8507, Japan.
Naoyuki KatayamaDepartment of Hematology and Oncology, Mie University Graduate School of Medicine, Mie 514-8507, Japan.
Mie University · JPMie University Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although immunotherapy has been demonstrated to be promising in triple-negative (TN) breast cancer (BC), most BC cases are classified as non-TN. To enrich the responders for immunotherapy regardless of their subtypes, classification based on tumor-infiltrating lymphocyte (TIL) levels and programmed death ligand-1 (PD-L1) status may be useful. However, this classification has not been fully applied to BC. Furthermore, suppressive subsets in the local tumor microenvironment, such as tumor-associated macrophages (TAMs), which promote tumor progression, cannot be ignored to overcome immunotherapy resistance. The aims of the present study were to classify primary BC cases based on the TIL levels and PD-L1 status, and to identify suppressive immune subsets in each categorized group. A retrospective analysis of 73 patients with invasive BC was performed. The frequency of TILs was evaluated in HE-stained slides (10% cutoff), and PD-L1 levels (SP142; 1% cutoff), as well as immune subsets (CD3

Indexed as

breast cancerCD204+ macrophagesprogrammed death ligand-1tumor-associated macrophagestumor-infiltrating lymphocytes

Identifiers

PMID33262828
PMCPMC7693484
OpenAlexW3101707196

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.