Evidence map›Paper›PMID 29700208›Full record

ArticleThe oncologist2018

Comprehensive Molecular Characterization of Young Chinese Patients with Lung Adenocarcinoma Identified a Distinctive Genetic Profile.

Helei Hou, Hua Zhu, Han Zhao, Weihua Yan, Yongjie Wang, Man Jiang, Bin Liu, Dong Liu, Na Zhou, Chuantao Zhang and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in The oncologist, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 2 pooled it
9.2field-weighted citation impact, top 2% 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

33 citing papers in PubMed, 2 syntheses or guidelines pooled it, 78 citations in OpenAlex.

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  13. Driver and actionable mutations in younger patients with lung cancer - are we searching properly?Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia · 2023
    Article
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  16. [Research Progress of Treatment for NSCLC in Young Patients].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2022
    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

18 authors at 4 institutions in 2 countries.

Helei HouDepartment of Medical Oncology, Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, People's Republic of China.
Hua ZhuDepartment of Medical Oncology, Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, People's Republic of China.
Han ZhaoDepartment of Pathology, Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, People's Republic of China.
Weihua YanDepartment of Pathology, Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, People's Republic of China.
Yongjie WangDepartment of Thoracic Surgery, Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, People's Republic of China.
Man JiangDepartment of Medical Oncology, Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, People's Republic of China.
Bin LiuDepartment of Medical Oncology, Affiliated Hospital of Shandong Academy of Medical Sciences, Jinan, People's Republic of China.
Dong LiuDepartment of Medical Oncology, Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, People's Republic of China.
Na ZhouDepartment of Medical Oncology, Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, People's Republic of China.
Chuantao ZhangDepartment of Medical Oncology, Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, People's Republic of China.
Pansong LiGeneplus-Beijing Institute, Beijing, People's Republic of China.
Lianpeng ChangGeneplus-Beijing Institute, Beijing, People's Republic of China.
Yanfang GuanGeneplus-Beijing Institute, Beijing, People's Republic of China.
Zhe WangDepartment of Clinical Laboratory, BGI-Shenzhen, Shenzhen, People's Republic of China.
Xiaoping ZhangDepartment of Clinical Laboratory, BGI-Shenzhen, Shenzhen, People's Republic of China.
Zhuokun LiBGI-Qingdao Institute, Qingdao, People's Republic of China.
Bingliang FangDepartment of Thoracic and Cardiovascular Surgery, University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Xiaochun ZhangDepartment of Medical Oncology, Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, People's Republic of China zxc9670@126.com.
Qingdao University · CNBGI Group (China) · CNAffiliated Hospital of Shandong Academy of Medical Sciences · CNThe University of Texas MD Anderson Cancer Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOccurrence at a younger age has been demonstrated to be associated with a distinct biology in non-small cell lung cancer. However, genomics and clinical characteristics among younger patients with lung adenocarcinoma remain to be determined. Here we studied the potentially targetable genetic alterations by next-generation sequencing (NGS) assay in young Chinese patients with lung adenocarcinoma. MATERIALS AND

methodsSeventy-one surgically resected lung adenocarcinoma tissue samples from patients aged less than 45 years were collected with informed consent from all patients. Targeted NGS assays were used to identify actionable genetic alterations in the cancer tissues. Additionally, the genomic and clinicopathologic characteristics of 106 patients with lung adenocarcinoma who received NGS testing over the same period were analyzed retrospectively.

resultsThe frequencies of targetable genetic alterations in 177 patients with lung adenocarcinoma were analyzed by defined age categories, which unveiled a distinctive molecular profile in the younger group, aged less than 45 years. Notably, higher frequency of

conclusionIn this study, NGS assay revealed a distinctive genetic profile in younger patients with adenocarcinoma. High frequency of concurrent IMPLICATIONS FOR PRACTICE: Further investigation is needed to understand the genomics and clinical characteristics of young patients with lung adenocarcinoma. In the present study, hybrid capture-based next-generation sequencing assays were used to identify targeted genetic alterations in young lung adenocarcinoma patients. Young patients with lung adenocarcinoma, aged less than 45 years, harbored a higher frequency of

Indexed as

Genetic ProfileAdenocarcinoma of LungChinaHumansLung NeoplasmsMiddle AgedGenetic profileLung adenocarcinomaNext‐generation sequencingYoung age

Identifiers

PMID29700208
PMCPMC6192606
OpenAlexW2800940448

What OpenQuestion holds

Textmetadata
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.