Evidence map›Paper›PMID 32178690›Full record

ArticleJournal of translational medicine2020

Glandular orientation and shape determined by computational pathology could identify aggressive tumor for early colon carcinoma: a triple-center study.

Meng-Yao Ji, Lei Yuan, Shi-Min Lu, Meng-Ting Gao, Zhi Zeng, Na Zhan, Yi-Juan Ding, Zheng-Ru Liu, Ping-Xiao Huang, Cheng Lu and 1 more

Open access · goldAbstract read
In one paragraph

Article in Journal of translational medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.1field-weighted citation impact, top 53% 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

4 citing papers in PubMed, 6 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

11 authors at 4 institutions in 1 country.

Meng-Yao JiDepartment of Gastroenterology, Wuhan University Renmin Hospital, Wuhan, Hubei, China.
Lei YuanDepartment of Information Center, Wuhan University Renmin Hospital, Wuhan, Hubei, China. yuanlei009@whu.edu.cn.
Shi-Min LuDepartment of Gastroenterology, Wuhan University Renmin Hospital, Wuhan, Hubei, China.
Meng-Ting GaoDepartment of Information Center, Wuhan University Renmin Hospital, Wuhan, Hubei, China.
Zhi ZengDepartment of Pathology, Wuhan University Renmin Hospital, Wuhan, Hubei, China.
Na ZhanDepartment of Pathology, Wuhan University Renmin Hospital, Wuhan, Hubei, China.
Yi-Juan DingDepartment of Gastroenterology, Wuhan University Renmin Hospital, Wuhan, Hubei, China.
Zheng-Ru LiuDepartment of Gastroenterology, Wuhan University Renmin Hospital, Wuhan, Hubei, China.
Ping-Xiao HuangDepartment of Gastroenterology, The Central Hospital of Wuhan, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Cheng LuCollege of Computer Science, Shaanxi Normal University, Xi'an, Shaanxi, China. chenglu@snnu.edu.cn.
Wei-Guo DongDepartment of Gastroenterology, Wuhan University Renmin Hospital, Wuhan, Hubei, China. dongweiguo_66@163.com.
Wuhan University · CNRenmin Hospital of Wuhan University · CNHuazhong University of Science and Technology · CNShaanxi Normal University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIdentifying the early-stage colon adenocarcinoma (ECA) patients who have lower risk cancer vs. the higher risk cancer could improve disease prognosis. Our study aimed to explore whether the glandular morphological features determined by computational pathology could identify high risk cancer in ECA via H&E images digitally.

methods532 ECA patients retrospectively from 2 independent data centers, as well as 113 from The Cancer Genome Atlas (TCGA), were enrolled in this study. Four tissue microarrays (TMAs) were constructed across ECA hematoxylin and eosin (H&E) stained slides. 797 quantitative glandular morphometric features were extracted and 5 most prognostic features were identified using minimum redundancy maximum relevance to construct an image classifier. The image classifier was evaluated on D2/D3 = 223, D4 = 46, D5 = 113. The expression of Ki67 and serum CEA levels were scored on D3, aiming to explore the correlations between image classifier and immunohistochemistry data and serum CEA levels. The roles of clinicopathological data and ECAHBC were evaluated by univariate and multivariate analyses for prognostic value.

resultsThe image classifier could predict ECA recurrence (accuracy of 88.1%). ECA histomorphometric-based image classifier (ECAHBC) was an independent prognostic factor for poorer disease-specific survival [DSS, (HR = 9.65, 95% CI 2.15-43.12, P = 0.003)]. Significant correlations were observed between ECAHBC-positive patients and positivity of Ki67 labeling index (Ki67Li) and serum CEA.

conclusionGlandular orientation and shape could predict the high risk cancer in ECA and contribute to precision oncology. Computational pathology is emerging as a viable and objective means of identifying predictive biomarkers for cancer patients.

Indexed as

Neoplasm Recurrence, LocalPrecision MedicineBiomarkers, TumorColonHumansNeoplasm StagingPrognosisRetrospective StudiesBiomarkers, TumorColon adenocarcinomaGland heterogeneityPrognosisQuantitative histopathology images

Identifiers

PMID32178690
PMCPMC7077008
OpenAlexW3011037969

What OpenQuestion holds

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LicenceCC BY
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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.