Evidence map›Paper›PMID 34136575›Full record

ArticleBioMed research international2021

Analysis of Multigene Mutations in Lung Adenocarcinoma in Zunyi.

Qingqing Ma, Dengming Ma, Mu Lin, Yadong Gong, Xiaojing Han, Yunhua Chen, Zhu Tang, Mubo Liu

RetractedOpen access · hybridAbstract readRetracted Publication
In one paragraph

Article in BioMed research international, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Qingqing MaDepartment of Central Laboratory, Guizhou Aerospace Hospital, Guizhou 563000, China.
Dengming MaDepartment of Anesthesiology, First People's Hospital of Mengyin County, China.
Mu LinDepartment of Central Laboratory, Guizhou Aerospace Hospital, Guizhou 563000, China.
Yadong GongDepartment of Central Laboratory, Guizhou Aerospace Hospital, Guizhou 563000, China.
Xiaojing HanDepartment of Central Laboratory, Guizhou Aerospace Hospital, Guizhou 563000, China.
Yunhua ChenDepartment of Central Laboratory, Guizhou Aerospace Hospital, Guizhou 563000, China.
Zhu TangDepartment of Central Laboratory, Guizhou Aerospace Hospital, Guizhou 563000, China.
Mubo LiuDepartment of Central Laboratory, Guizhou Aerospace Hospital, Guizhou 563000, China.ORCID https://orcid.org/0000-0002-4884-3037

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveDriver gene mutation in lung adenocarcinoma patients in Zunyi and its relationship with clinical features were probed in this investigation.

methodsIn total, with 244 patients with lung adenocarcinoma as study subjects, including 141 males and 103 females, amplification-refractory mutation system-polymerase chain reaction (ARMS-PCR) was utilized for detecting multigene mutations. Subsequently, the relationship between gene mutation and clinical characteristics was analyzed.

resultsThe total mutation rate of driver genes was 65.17%, including 48.36% EGFR, 6.15% KRAS, 5.74% ALK, 2.05% HER-2, 1.23% ROS1, 0.82% RET, 0.41% NRAS, and 0.41% BRAF. Among EGFR mutations, 47.46% were EGFR-19-deletion, 42.37% EGFR-21-L858R mutation, 4.24% EGFR-20-T790M mutation, 2.54% EGFR-21-L861Q mutation, 2.54% EGFR-20-insertion, and 0.85% EGFR-18-G719X mutation. Both female patients and nonsmoking patients with lung adenocarcinoma had a higher rate of EGFR mutation. Additionally, 15 patients with multiple mutations in EGFR, including 13 patients with 2 mutations in EGFR and 2 patients with 3 mutations in EGFR, were found.

conclusionAmong driver gene mutations in patients with lung adenocarcinoma in Zunyi, EGFR mutation has the highest incidence, followed by ALK fusion and KRAS mutation. Although both mutations and multisite mutations in the other driver genes account for a low proportion, they still have great clinical significance. Multigene mutation detection contributes to the rapid screening of patients with lung adenocarcinoma who respond to targeted therapy.

Indexed as

MutationAdenocarcinoma of LungAgedChinaDNA Mutational AnalysisErbB ReceptorsFemaleHumansIncidenceLung NeoplasmsMaleMiddle AgedOncogenesPolymerase Chain ReactionProto-Oncogene ProteinsEGFR protein, humanErbB ReceptorsProto-Oncogene Proteins

Identifiers

PMID34136575
PMCPMC8179774
OpenAlexW3170432298

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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.