Evidence map›Paper›PMID 31769218›Full record

ArticleCancer medicine2020

Analysis of the clinicopathological characteristics, genetic phenotypes, and prognostic of pure mucinous adenocarcinoma.

Zhencong Chen, Ming Li, Ke Ma, Guoguo Shang, Jiaqi Liang, Jiacheng Yin, Jizhuang Luo, Cheng Zhan, Yu Shi, Qun Wang

Abstract read
In one paragraph

Article in Cancer medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
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

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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

12 citing papers in PubMed.

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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

10 authors.

Zhencong ChenDepartment of Thoracic of Zhongshan Hospital, Fudan University, Shanghai, China.
Ming LiDepartment of Thoracic of Zhongshan Hospital, Fudan University, Shanghai, China.
Ke MaDepartment of Thoracic of Zhongshan Hospital, Fudan University, Shanghai, China.
Guoguo ShangDepartment of Pathology of Zhongshan Hospital, Fudan University, Shanghai, China.
Jiaqi LiangDepartment of Thoracic of Zhongshan Hospital, Fudan University, Shanghai, China.
Jiacheng YinDepartment of Thoracic of Zhongshan Hospital, Fudan University, Shanghai, China.
Jizhuang LuoDepartment of Thoracic of Zhongshan Hospital, Fudan University, Shanghai, China.
Cheng ZhanDepartment of Thoracic of Zhongshan Hospital, Fudan University, Shanghai, China.ORCID 0000-0001-8745-9276
Yu ShiDepartment of Thoracic of Zhongshan Hospital, Fudan University, Shanghai, China.
Qun WangDepartment of Thoracic of Zhongshan Hospital, Fudan University, Shanghai, China.ORCID 0000-0003-4853-1727

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPrimary pure mucinous adenocarcinoma of the lung (PMA) is a rare subtype. However, correlations between clinicopathological features and genetic phenotypes with survival have not been described comprehensively.

methodsPure mucinous adenocarcinoma patient information collected from the Surveillance, Epidemiology, and End Results (SEER) database, the Department of Thoracic Surgery, Zhongshan Hospital, Fudan University (FDZSH), and the Cancer Genome Atlas (TCGA) were extracted, evaluated, and compared with other lung adenocarcinomas (LUAD) patient data. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes pathway analyses were performed to explore the functional importance of underlying molecular changes. Overall survival (OS) was evaluated with the Kaplan-Meier method. Univariate and multivariate analysis through Cox proportional hazard regression identified risk factors that predicted OS, and the results were used to construct a nomogram to predict OS for PMA patients.

resultsOverall, 3622 patients, 41 patients, and 15 patients with PMA were identified from the SEER, FDZSH, and TCGA databases, respectively. There were 345 differentially expressed genes, 30 differentially mutated genes and 72 differentially methylated genes were identified between PMA and other LUAD samples. In the SEER database, PMA had a better prognosis compared to other LUAD. Compared with patients with other LUAD, patients with PMA exhibited unique clinicopathological features, including fewer grade III/IV tumors, less pleural invasion, more early-stage cancer, and more lower lobe carcinomas. Multivariate analyses showed that age, race, T stage, N stage, surgery, and chemotherapy were independent risk factors. The nomogram had a calibration index of 0.724.

conclusionsOur research identified unique clinicopathological characteristics and genetic phenotypes for PMA and other LUAD. The nomogram accurately predicted OS.

Indexed as

NomogramsAdenocarcinoma, MucinousAgedBiomarkers, TumorDatabases, FactualFemaleFollow-Up StudiesGenotypeHumansLung NeoplasmsMaleMiddle AgedNeoplasm StagingPhenotypeRetrospective StudiesRisk FactorsBiomarkers, Tumorclinicopathological featuresgenetic analysisnomogrampure mucinous adenocarcinomathe surveillance, epidemiology, and end results

Identifiers

PMID31769218
PMCPMC6970056

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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.