Deciphering the Dynamics of EGFR-TKI Resistance in Lung Cancer: Insights from Bibliometric Analysis

被引:1
|
作者
Zhou, Yinxue [1 ]
Wu, Tingyu [2 ]
Sun, Jiaxing [1 ]
Bi, Huanhuan [1 ]
Xiao, Yuting [1 ]
Shao, Yanmei [1 ]
Han, Weizhong [1 ]
Wang, Hongmei [1 ]
机构
[1] Qingdao Univ, Affiliated Hosp, Dept Resp & Crit Care Med, Qingdao, Peoples R China
[2] Qingdao Univ, Affiliated Hosp, Dept Joint Surg, Qingdao, Peoples R China
来源
DRUG DESIGN DEVELOPMENT AND THERAPY | 2024年 / 18卷
关键词
EGFR-TKI; resistance; lung cancer; bibliometric; citespace; VOSviewer; ACQUIRED-RESISTANCE; OPEN-LABEL; KINASE INHIBITORS; GEFITINIB; MUTATION; OSIMERTINIB; MULTICENTER; SCIENCE; CHEMOTHERAPY; WEB;
D O I
10.2147/DDDT.S478910
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Background: EGFR-TKI resistance poses a significant challenge in the treatment landscape of non-small cell lung cancer (NSCLC), prompting extensive research into mechanisms and therapeutic strategies. In this study, we conduct a bibliometric analysis to elucidate evolving research hotspots and trends in EGFR-TKI resistance, offering insights for clinical interventions and scientific inquiries. Methods: Publications spanning from 1996 to 2024, focusing on EGFR-TKI resistance in NSCLC, were sourced from the Web of Science Core Collection. Utilizing VOSviewer 1.6.19, CiteSpace 6.2. R2, and Scimago Graphica 1.0.35, we analyzed these articles to identify countries/regions and institutions, Journals, publications, key contributors, collaborations, and emerging topics. Results: An analysis of 8051 articles by 38,215 researchers from 86 countries shows growing interest in EGFR-TKI resistance mechanisms. Since 1996, publications have steadily increased, surpassing 500 per year after 2016, with a sharp rise in citations. Research articles make up 84% of publications, emphasizing scholarly focus. Global collaboration, especially among researchers in China, the US, and Japan, is strong. Leading institutions like Dana-Farber and Harvard, along with journals such as "Lung Cancer", are key in sharing findings. Professors Yi-Long Wu and William Pao are prominent contributors. Keyword analysis reveals core themes, including first-generation EGFR-TKIs, emerging agents like osimertinib, and research on the T790M mutation. Conclusion: EGFR-TKI resistance remains a critical issue in NSCLC treatment, driving ongoing research efforts worldwide. Focusing future research on clear identification of resistance mechanisms will guide post-resistance treatment strategies, necessitating further exploration, alongside the validation of emerging drugs through clinical trials. Moreover, "chemo+" treatments following EGFR-TKI resistance require more clinical data and real-world evidence for assessing safety and patient outcomes. As research advances, a multidisciplinary approach will be key to overcoming these challenges. Continued innovation in treatment could greatly enhance patient survival and quality of life.
引用
收藏
页码:4327 / 4343
页数:17
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