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
相关论文
共 50 条
  • [41] Bevacizumab to combat EGFR-TKI resistance in a patient with advanced non-small cell lung cancer harboring an EGFR mutation: A case report
    Wang, Zhiyi
    Zhou, Pu
    Li, Guanghui
    ONCOLOGY LETTERS, 2016, 12 (01) : 356 - 360
  • [42] Apatinib to combat EGFR-TKI resistance in an advanced non-small cell lung cancer patient with unknown EGFR status: a case report
    Peng, Yanmei
    Cui, Huijuan
    Liu, Zhe
    Liu, Daiwei
    Liu, Fan
    Song, Yazhong
    Duan, Hua
    Qiu, Yuqin
    Li, Qiang
    ONCOTARGETS AND THERAPY, 2017, 10 : 2289 - 2295
  • [43] Combination of EGFR-TKI and Chemotherapy Versus EGFR-TKI Monotherapy as Neoadjuvant Treatment of Stage III-N2 EGFR-Mutant Non-Small Cell Lung Cancer
    Xu, Yingqi
    Ji, Hao
    Zhang, Yidan
    Xiong, Liwen
    Han, Baohui
    Zhong, Hua
    Xu, Jianlin
    Zhong, Runbo
    ONCOLOGIST, 2024, 29 (07) : e932 - e940
  • [44] Mutation abundance affects the therapeutic efficacy of EGFR-TKI in patients with advanced lung adenocarcinoma: A retrospective analysis
    Wang, Huijuan
    Zhang, Mina
    Tang, Wanyu
    Ma, Jie
    Wei, Bing
    Niu, Yuanyuan
    Zhang, Guowei
    Li, Peng
    Yan, Xiangtao
    Ma, Zhiyong
    CANCER BIOLOGY & THERAPY, 2018, 19 (08) : 687 - 694
  • [45] Combining EGFR-TKI With SAHA Overcomes EGFR-TKI-Acquired Resistance by Reducing the Protective Autophagy in Non-Small Cell Lung Cancer
    Cao, Peijun
    Li, Yongwen
    Shi, Ruifeng
    Yuan, Yin
    Gong, Hao
    Zhu, Guangsheng
    Zhang, Zihe
    Chen, Chen
    Zhang, Hongbing
    Liu, Minghui
    Pan, Zhenhua
    Liu, Hongyu
    Chen, Jun
    FRONTIERS IN CHEMISTRY, 2022, 10
  • [46] A novel strategy of EGFR-TKI combined chemotherapy in the treatment of human lung cancer with EGFR-sensitive mutation
    Zhang, Lanlin
    Qi, Yuan
    Xing, Kailin
    Qian, Song
    Zhang, Ping
    Wu, Xianghua
    ONCOLOGY REPORTS, 2018, 40 (02) : 1046 - 1054
  • [47] Expression of selected gene for acquired drug resistance to EGFR-TKI in lung adenocarcinoma
    Uramoto, Hidetaka
    Shimokawa, Hidehiko
    Hanagiri, Takeshi
    Kuwano, Michihiko
    Ono, Mayumi
    LUNG CANCER, 2011, 73 (03) : 361 - 365
  • [48] Liver X receptor agonist T0901317 reverses resistance of A549 human lung cancer cells to EGFR-TKI treatment
    Cao, Haixia
    Yu, Shaorong
    Chen, Dan
    Jing, Changwen
    Wang, Zhuo
    Ma, Rong
    Liu, Siwen
    Ni, Jie
    Feng, Jifeng
    Wu, Jianzhong
    FEBS OPEN BIO, 2017, 7 (01): : 35 - 43
  • [49] Association between EGFR-TKI Resistance and Efficacy of Radiotherapy for Brain Metastases from EGFR-mutant Lung Adenocarcinoma
    Hirata, Hidenari
    Nakamura, Katsumasa
    Kunitake, Naonobu
    Shioyama, Yoshiyuki
    Sasaki, Tomonari
    Ohga, Saiji
    Nonoshita, Takeshi
    Yoshitake, Tadamasa
    Asai, Kaori
    Inoue, Kouji
    Nagashima, Akira
    Ono, Minoru
    Honda, Hiroshi
    ANTICANCER RESEARCH, 2013, 33 (04) : 1649 - 1655
  • [50] The Impact of Sequence of Chemotherapy and EGFR-TKI Treatment on Different EGFR Mutation Lung Adenocarcinoma
    Chung, Fu-Tsai
    Ho, Ming-Yun
    Fang, Yueh-Fu
    Hshieh, Meng-Heng
    Wang, Tsai-Yu
    Kuo, Chih-Hsi
    Chen, Hao-Cheng
    Wang, Chun-Hwa
    Lin, Shu-Min
    Yu, Chih-Teng
    Lin, Horng-Chyuan
    Kuo, Han-Pin
    BIOMED RESEARCH INTERNATIONAL, 2015, 2015