Evidence map›Paper›PMID 33219256›Full record

ArticleScientific reports2020

Comprehensive genomic profile of Chinese lung cancer patients and mutation characteristics of individuals resistant to icotinib/gefitinib.

Yanhong Shang, Xiaofang Li, Weiwei Liu, Xiaoliang Shi, Shaohua Yuan, Ran Huo, Guotao Fang, Xiao Han, Jingnan Zhang, Kunjie Wang and 4 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.4field-weighted citation impact, top 9% 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

26 citing papers in PubMed, 36 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

14 authors at 2 institutions in 1 country.

Yanhong ShangDepartment of Medical Oncology, Affiliated Hospital of Hebei University, No. 648, Dongfeng East Road, Baoding City, 071000, Hebei, People's Republic of China. hdfyzlnk@sina.com.
Xiaofang LiDepartment of Medical Oncology, Affiliated Hospital of Hebei University, No. 648, Dongfeng East Road, Baoding City, 071000, Hebei, People's Republic of China.
Weiwei LiuDepartment of Medical Oncology, Affiliated Hospital of Hebei University, No. 648, Dongfeng East Road, Baoding City, 071000, Hebei, People's Republic of China.
Xiaoliang ShiOrigiMed Co. Ltd, Shanghai, 201114, People's Republic of China.
Shaohua YuanOrigiMed Co. Ltd, Shanghai, 201114, People's Republic of China.
Ran HuoDepartment of Medical Oncology, Affiliated Hospital of Hebei University, No. 648, Dongfeng East Road, Baoding City, 071000, Hebei, People's Republic of China.
Guotao FangDepartment of Medical Oncology, Affiliated Hospital of Hebei University, No. 648, Dongfeng East Road, Baoding City, 071000, Hebei, People's Republic of China.
Xiao HanDepartment of Medical Oncology, Affiliated Hospital of Hebei University, No. 648, Dongfeng East Road, Baoding City, 071000, Hebei, People's Republic of China.
Jingnan ZhangDepartment of Medical Oncology, Affiliated Hospital of Hebei University, No. 648, Dongfeng East Road, Baoding City, 071000, Hebei, People's Republic of China.
Kunjie WangDepartment of Medical Oncology, Affiliated Hospital of Hebei University, No. 648, Dongfeng East Road, Baoding City, 071000, Hebei, People's Republic of China.
Zhengyue DouDepartment of Medical Oncology, Affiliated Hospital of Hebei University, No. 648, Dongfeng East Road, Baoding City, 071000, Hebei, People's Republic of China.
Yan ZhangDepartment of Oncology, The First Hospital of Shijiazhuang City, No.36, Fanxi Road, Chang'an District, Shijiazhuang City, 050000, Hebei, People's Republic of China.
Aimin ZangDepartment of Medical Oncology, Affiliated Hospital of Hebei University, No. 648, Dongfeng East Road, Baoding City, 071000, Hebei, People's Republic of China.
Lin ZhangOrigiMed Co. Ltd, Shanghai, 201114, People's Republic of China.
Affiliated Hospital of Hebei University · CNFirst Hospital of Shijiazhuang · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lung cancer is the leading causes of cancer-related death worldwide. Precise treatment based on next-generation sequencing technology has shown advantages in the diagnosis and treatment of lung cancer. This cohort study included 371 lung cancer patients. The lung cancer subtype was related to the smoking status and sex of the patients. The most common mutated genes were TP53 (62%), EGFR (55%), and KRAS (11%). The mutation frequencies of EGFR, TP53, PIK3CA, NFE2L2, KMT2D, FGFR1, CCND1, and CDKN2A were significantly different between lung adenocarcinoma and lung squamous cell carcinoma. We identified the age-associated mutations in ALK, ERBB2, KMT2D, RBM10, NRAS, NF1, PIK3CA, MET, PBRM1, LRP2, and CDKN2B; smoking-associated mutations in CDKN2A, FAT1, FGFR1, NFE2L2, CCNE1, CCND1, SMARCA4, KEAP1, KMT2C, and STK11; tumor stage-associated mutations in ARFRP1, AURKA, and CBFB; and sex-associated mutations in EGFR. Tumor mutational burden (TMB) is associated with tumor subtype, age, sex, and smoking status. TMB-associated mutations included CDKN2A, LRP1B, LRP2, TP53, and EGFR. EGFR amplification was commonly detected in patients with acquired lcotinib/gefitinib resistance. DNMT3A and NOTCH4 mutations may be associated with the benefit of icotinib/gefitinib treatment.

Indexed as

MutationAdultAgedAged, 80 and overAntineoplastic AgentsAsian PeopleBiomarkers, TumorChinaCrown EthersDrug Resistance, NeoplasmFemaleGefitinibHumansLung NeoplasmsMaleMiddle AgedAntineoplastic AgentsBiomarkers, TumorCrown EthersGefitinibicotinibQuinazolines

Identifiers

PMID33219256
PMCPMC7679461
OpenAlexW3104284569

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.