Evidence map›Paper›PMID 35242380›Full record

ArticleJournal of thoracic disease2022

The co-mutation of

Yi Zhang, Shirong Li, Zhi Lyu, Jinghuang Cai, Naishan Zheng, Yanping Li, Tianwen Xu, Huiqing Zeng

Open access · diamondAbstract read
In one paragraph

Article in Journal of thoracic disease, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

18 citing papers in PubMed, 23 citations in OpenAlex.

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  8. A gene set enrichment analysis for cancer hallmarks.Journal of pharmaceutical analysis · 2025
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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

8 authors at 4 institutions in 1 country.

Yi Zhang *Department of Cardiothoracic Surgery, Zhangzhou Hospital Affiliated of Fujian Medical University, Zhangzhou, China.
Shirong Li *Department of Respiratory, Wuhu Hospital Affiliated to East China Normal University, Wuhu, China.
Zhi Lyu *Department of Senior Cadres Ward, Zhongshan Hospital of Xiamen University, School of Medicine, Xiamen University, Xiamen, China.
Jinghuang CaiDepartment of Pulmonary and Critical Care Medicine, Zhongshan Hospital of Xiamen University, School of Medicine, Xiamen University, Xiamen, China.
Naishan ZhengThe Third Clinical Medical College, Fujian Medical University, Fuzhou, China.
Yanping LiThe Third Clinical Medical College, Fujian Medical University, Fuzhou, China.
Tianwen XuDepartment of Medical Oncology, the Second Affiliated Hospital of Fujian Medical University, Quanzhou, China.
Huiqing ZengDepartment of Pulmonary and Critical Care Medicine, Zhongshan Hospital of Xiamen University, School of Medicine, Xiamen University, Xiamen, China.
Fujian Medical University · CNZhongshan Hospital of Xiamen University · CNEast China Normal University · CNZhangzhou Municipal Hospital of Fujian Province · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLung cancer is the leading cause of cancer mortality in China. The clinicopathologic features and genetic profile of Chinese lung cancer patients need to be investigated. This study evaluated the gene mutation profile, analyzed the frequency of concurrent genes in epidermal growth factor receptor (EGFR)-mutant non-small cell lung cancer (NSCLC) patients, and determined its prognostic value.

methodsWe collected the clinical data from 151 initially diagnosed patients NSCLC. Tumor samples underwent targeted next-generation sequencing (NGS). Progression-free survival (PFS) and overall survival (OS) were analyzed using the Kaplan-Meier method.

resultsAmong the 151 participants, the mutational profile revealed alterations in 29 genes, where

conclusionsWe described the genetic profiles of NSCLC and compared the difference in genetic profiles between LUAD and LUSC. The concomitant genetic alterations might be a poor prognostic factor for patients with

Indexed as

epidermal growth factor receptor (EGFR)Non-small cell lung cancer (NSCLC)prognosistumor mutational burden (TMB)

Identifiers

PMID35242380
PMCPMC8828510
OpenAlexW4207054482

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.