Evidence map›Paper›PMID 35116479›Full record

ArticleTranslational cancer research2021

Prognostic role of epidermal growth factor receptor mutation status in patients with de novo lung adenocarcinoma.

Bo Li, Xiaolu Ren, Hongxia Guo, Yi Guo, Fei Han, Xiaolian Wen, Jing Wu, Xiaomin Li, Yuejun Ren, Xiaoyun Hu and 1 more

Open access · diamondAbstract read
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Article in Translational cancer research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

11 authors at 4 institutions in 1 country.

Bo Li *Department of Radiation Oncology, Shanxi Cancer Hospital, Taiyuan, China.
Xiaolu Ren *Department of Radiation Oncology, Shanxi Cancer Hospital, Taiyuan, China.
Hongxia GuoDepartment of Oncology, Shanxi Bethune Hospital, Taiyuan, China.
Yi GuoDepartment of Respiration, Shanxi Cancer Hospital, Taiyuan, China.
Fei HanDepartment of Thoracic Surgery, Shanxi Cancer Hospital, Taiyuan, China.
Xiaolian WenDepartment of Hematology, Shanxi Cancer Hospital, Taiyuan, China.
Jing WuDepartment of Radiation Oncology, Shanxi Cancer Hospital, Taiyuan, China.
Xiaomin LiDepartment of Radiation Oncology, Shanxi Cancer Hospital, Taiyuan, China.
Yuejun RenDepartment of Radiation Oncology, Shanxi Cancer Hospital, Taiyuan, China.
Xiaoyun HuDepartment of Respiration, First Hospital of Shanxi Medical University, Taiyuan, China.
Zhihong LiuDepartment of Respiration, First Hospital of Shanxi Medical University, Taiyuan, China.
Shanxi Provincial Cancer Hospital · CNFirst Hospital of Shanxi Medical University · CNShanxi Academy of Medical Sciences · CNShanxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTo explore the relationship between the status of epidermal growth factor receptor (EGFR) and overall survival (OS) in de novo lung adenocarcinoma.

methodsWe retrospectively analyzed 291 lung adenocarcinoma subjects with exact EGFR status. The cases were divided into a mutant-type group (124 patients) and wild-type group (167 patients) according to the status of EGFR. The general information, OS, and possible risk factors influencing the OS were also evaluated.

resultsThe EGFR mutation rate was 42.6% (124/291 patients), and there were statistically significant differences in gender, smoking history, and OS (P<0.05), but no significant difference in diagnosed age, alcohol history, TNM stage, clinical stage, and immunohistochemistry between the two groups (P>0.05). The most common subtypes of EGFR mutations were exon 19 and exon 21. The median OS of the total population was 30.20 months [95% confidence interval (CI): 25.94-34.46 months] and the OS in the mutant-type group was better than in the wild-type group (P<0.001). Cox regression demonstrated that N stage, M stage, and EGFR status were the risk factors for OS in de novo lung adenocarcinoma patients (P<0.001), and the relative risk were 1.398 (95% CI: 1.214-1.609), 2.427 (95% CI: 1.780-3.310), and 2.030 (95% CI: 1.528-2.699), respectively.

conclusionsThe OS of EGFR mutant individuals was better than that of wild-type patients in de novo lung adenocarcinoma patients. EGFR mutation may be a useful prognostic indicator in lung adenocarcinoma.

Indexed as

epidermal growth factor receptor (EGFR)Lung adenocarcinomaoverall survival (OS)

Identifiers

PMID35116479
PMCPMC8798523
OpenAlexW3145765392

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