Evidence map›Paper›PMID 33679868›Full record

ArticleFrontiers in genetics2020

The Comprehensive Analyses of Genomic Variations and Assessment of TMB and PD-L1 Expression in Chinese Lung Adenosquamous Carcinoma.

Yong Cheng, Yanxiang Zhang, Yuwei Yuan, Jiao Wang, Ke Liu, Bin Yu, Li Xie, Chao Ou-Yang, Lin Wu, Xiaoqun Ye

Open access · goldAbstract read
In one paragraph

Article in Frontiers in genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

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  5. Targeted therapy for rare lung cancers: Status, challenges, and prospects.Molecular therapy : the journal of the American Society of Gene Therapy · 2023
    Review
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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 at 3 institutions in 1 country.

Yong ChengDepartment of Respiratory Diseases, The Second Affiliated Hospital of Nanchang University, Nanchang, China.
Yanxiang ZhangBerry Oncology Corporation, Beijing, China.
Yuwei YuanBerry Oncology Corporation, Beijing, China.
Jiao WangDepartment of Respiratory Diseases, The Second Affiliated Hospital of Nanchang University, Nanchang, China.
Ke LiuBerry Oncology Corporation, Beijing, China.
Bin YuDepartment of Respiratory Diseases, The Second Affiliated Hospital of Nanchang University, Nanchang, China.
Li XieDepartment of Respiratory Diseases, The Second Affiliated Hospital of Nanchang University, Nanchang, China.
Chao Ou-YangDepartment of Respiratory Diseases, The Second Affiliated Hospital of Nanchang University, Nanchang, China.
Lin WuBerry Oncology Corporation, Beijing, China.
Xiaoqun YeDepartment of Respiratory Diseases, The Second Affiliated Hospital of Nanchang University, Nanchang, China.
Nanchang University · CNBerry Oncology (China) · CNSecond Affiliated Hospital of Nanchang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The poor prognosis and fewer treatment option is a current clinical challenge for patients with lung adenosquamous carcinoma (ASC). The previous studies reported that tumor mutational burden (TMB, numbers of mutation per Megabase) is a predictor of clinical response in trials of multiple cancer types, while fewer studies assessed the relationship between TMB level and clinical features and outcomes of lung ASC. Herein, the present study enrolled Chinese patients with lung ASC. DNA was extracted from formalin-fixed paraffin-embedded tumor samples and subjected to next generation sequencing (NGS), and the 457 cancer related genes were evaluated. The results demonstrated that 95 unique genes with somatic variations were identified in the enrolled patients. The top three of high frequency gene mutations were

Indexed as

adenosquamous carcinomaEGFRlungnext generation sequencingPD-L1somatic variationsTMB

Identifiers

PMID33679868
PMCPMC7925901
OpenAlexW3133331314

What OpenQuestion holds

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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.