Evidence map›Paper›PMID 34367978›Full record

ArticleFrontiers in oncology2021

Large-Section Histopathology Can Better Indicate the Immune Microenvironment and Predict the Prognosis of Pancreatic Ductal Adenocarcinoma Than Small-Section Histopathology.

Guiling Ding, Meng Guo, Yelin Yang, Chen Sun, Shengyong Wu, Xingchen Liu, Jin Wang, Hui Jiang, Yanfang Liu, Jianming Zheng

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 47% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
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

10 authors at 3 institutions in 1 country.

Guiling DingDepartment of Pathology, Shanghai General Hospital Affiliated to Shanghai Jiaotong University, Shanghai, China.
Meng GuoNational Key Laboratory of Medical Immunology & Institute of Immunology, Naval Medical University (Second Military Medical University), Shanghai, China.
Yelin YangDepartment of Pathology, Changhai Hospital Affiliated to Navy Medical University (Second Military Medical University), Shanghai, China.
Chen SunDepartment of Pathology, Changhai Hospital Affiliated to Navy Medical University (Second Military Medical University), Shanghai, China.
Shengyong WuDepartment of Health Statistics, Naval Medical University (Second Military Medical University), Shanghai, China.
Xingchen LiuDepartment of Pathology, Changhai Hospital Affiliated to Navy Medical University (Second Military Medical University), Shanghai, China.
Jin WangDepartment of Pathology, Changhai Hospital Affiliated to Navy Medical University (Second Military Medical University), Shanghai, China.
Hui JiangDepartment of Pathology, Changhai Hospital Affiliated to Navy Medical University (Second Military Medical University), Shanghai, China.
Yanfang LiuDepartment of Pathology, Changhai Hospital Affiliated to Navy Medical University (Second Military Medical University), Shanghai, China.
Jianming ZhengDepartment of Pathology, Changhai Hospital Affiliated to Navy Medical University (Second Military Medical University), Shanghai, China.
Second Military Medical University · CNChanghai Hospital · CNShanghai Jiao Tong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is a highly malignant tumor and is insensitive to radiotherapy and chemotherapy, as it is highly correlated with its complex tumor microenvironment (TME). A comprehensive description of PDAC's immune microenvironment at the pathological level has not been reported, thus limiting its treatment. Previous studies have shown that large-section histopathology (LSH) can reveal the complete structure and margin of the tumor on a single slice and effectively reflect intratumoral heterogeneity. LSH, as opposed to classic small-section histopathology (SSH), can also be used to explore the infiltration state of immune cells in different regions. In the current study, EnVision immunohistochemical staining was used to explore the panoramic distribution of CD4-, CD8-, CD15-, CD20-, and CD56 (surface markers of helper T cells, cytotoxic T cells, neutrophils, B cells, and NK cells, respectively)-positive cells in 102 pairs of paraffin wax-embedded PDAC samples (LSH

Indexed as

immune celllarge histological sectionsnomogrampancreatic ductal adenocarcinomaprognosistumor microenvironment

Identifiers

PMID34367978
PMCPMC8340684
OpenAlexW3178998354

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.