Continued EGFR-TKIs treatment promotes the survival of elderly patients with acquired resistance to EGFR-TKIs therapy

被引:0
|
作者
Wang, P. [1 ]
Zhang, D. [1 ]
Li, X. -M. [1 ]
Guo, X. -G. [1 ]
Sun, B. -J. [2 ]
Fang, X. -Q. [2 ]
Qu, G. -P. [2 ]
An, L. [2 ]
Liu, C. -T. [2 ]
机构
[1] Chinese Peoples Liberat Army Gen Hosp, Dept Nanlou Med Oncol, Beijing, Peoples R China
[2] Chinese Peoples Liberat Army Gen Hosp, Dept Nanlou Resp Dis, Beijing, Peoples R China
关键词
Continued EGFR-TKIs; Progressive disease; NSCLC; Elderly patients; Non-dramatic progression; CELL LUNG-CANCER; TYROSINE KINASE INHIBITORS; 1ST-LINE TREATMENT; OPEN-LABEL; ERLOTINIB; GEFITINIB; CHEMOTHERAPY; DISCONTINUATION; MULTICENTER; STATISTICS;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
OBJECTIVE: Continued EGFR-TKIs treatment is still controversial for NSCLC patients with activating EGFR mutations, who acquire resistance to the drug. Of these patients, elderly ones were worth to be investigated to further examine efficacy of continued EGFR-TKIs treatment. PATIENTS AND METHODS: A total of 232 NSCLC patients (70-year-old) were recruited from the Chinese People's Liberation Army General Hospital between January 1, 2009, and July 31, 2014. And 44 patients were qualified for further retrospectively investigated, which were divided into dramatic and non-dramatic progression groups based on the characteristics of progression during first-line EGFR-TKIs treatment. And they were also divided into two groups: continued EGFR-TKIs group and discontinued EGFR-TKIs group. Subsequently, progression-free survival (PFS), post-progression survival (PPS), and overall survival (OS) of these groups were investigated by multivariate analysis. RESULTS: Median OS (28.9 months vs. 23.2 months, p = 0.46) and median PPS (16.9 months vs. 4.4 months, p = 0.216) were both not significantly different between continued EGFR-TKIs groups and discontinued ones. However, when focusing on patients with non-dramatic progression, the median OS (29.0 months vs. 23.2 months, p = 0.039) and median PPS (21.3 months vs. 3.9 months, p = 0.001) were significantly longer in the continued EGFR-TKIs patients than discontinued ones. DISCUSSION: Continued EGFR-TKIs beyond PD may be a good option for elderly patients with non-dramatic progression. The characteristic of progression after first-line EGFR-TKIs treatment should be taken into account to determine which part of patients is suitable for continued EGFR-TKIs treatment, especially for the speed of progression. CONCLUSION: Continued EGFR-TKIs treatment promotes the survival of elderly patients with acquired resistance to EGFR-TKIs therapy.
引用
收藏
页码:2450 / 2459
页数:10
相关论文
共 50 条
  • [1] EGFR-TKIs plus local therapy demonstrated survival benefit than EGFR-TKIs alone in EGFR-mutant NSCLC patients with oligometastatic or oligoprogressive liver metastases
    Jiang, Tao
    Chu, Qian
    Wang, Huijuan
    Zhou, Fei
    Gao, Guanghui
    Chen, Xiaoxia
    Li, Xuefei
    Zhao, Chao
    Xu, Qinghua
    Li, Wei
    Wu, Fengying
    Xiong, Anwen
    Zhao, Jing
    Xu, Yaping
    Su, Chunxia
    Ren, Shengxiang
    Zhou, Caicun
    Hirsch, Fred R.
    INTERNATIONAL JOURNAL OF CANCER, 2019, 144 (10) : 2605 - 2612
  • [2] EGFR-TKIs plus bevacizumab demonstrated survival benefit than EGFR-TKIs alone in patients with EGFR-mutant NSCLC and multiple brain metastases
    Jiang, Tao
    Zhang, Yongchang
    Li, Xuefei
    Zhao, Chao
    Chen, Xiaoxia
    Su, Chunxia
    Ren, Shengxiang
    Yang, Nong
    Zhou, Caicun
    EUROPEAN JOURNAL OF CANCER, 2019, 121 : 98 - 108
  • [3] EGFR-TKIs or EGFR-TKIs combination treatments for untreated advanced EGFR-mutated NSCLC: a network meta-analysis
    Liu, Ao
    Wang, Xiaoming
    Wang, Lian
    Zhuang, Han
    Xiong, Liubo
    Gan, Xiao
    Wang, Qian
    Tao, Guanyu
    BMC CANCER, 2024, 24 (01)
  • [4] Microwave ablation combined with EGFR-TKIs versus only EGFR-TKIs in advanced NSCLC patients with EGFR-sensitive mutations
    Wei, Zhigang
    Ye, Xin
    Yang, Xia
    Zheng, Aimin
    Huang, Guanghui
    Li, Wenhong
    Wang, Jiao
    Han, Xiaoying
    Meng, Min
    Ni, Yang
    ONCOTARGET, 2017, 8 (34) : 56714 - 56725
  • [5] EGFR-TKIs in adjuvant treatment of lung cancer: to give or not to give?
    Milovancev, Aleksandar
    Stojsic, Vladimir
    Zaric, Bojan
    Kovacevic, Tomi
    Sarcev, Tatjana
    Perin, Branislav
    Zarogoulidis, Konstantinos
    Tsirgogianni, Katerina
    Freitag, Lutz
    Darwiche, Kaid
    Tsavlis, Drosos
    Zissimopoulos, Athanasios
    Stratakos, Grigoris
    Zarogoulidis, Paul
    ONCOTARGETS AND THERAPY, 2015, 8 : 2915 - 2921
  • [6] Combination of EGFR-TKIs with chemotherapy versus chemotherapy or EGFR-TKIs alone in advanced NSCLC patients with EGFR mutation
    Wen, Miaomiao
    Xia, Jinghua
    Sun, Ying
    Wang, Xuejiao
    Fu, Xianghui
    Zhang, Yanning
    Zhang, Zhipei
    Zhou, Yongan
    Li, Xiaofei
    BIOLOGICS-TARGETS & THERAPY, 2018, 12 : 183 - 190
  • [7] Bevacizumab Combined with Continuation of EGFR-TKIs in NSCLC Beyond Gradual Progression
    Xu, Ziyi
    Teng, Fei
    Hao, Xuezhi
    Li, Junling
    Xing, Puyuan
    CANCER MANAGEMENT AND RESEARCH, 2022, 14 : 1891 - 1902
  • [8] Serum proteomic study on EGFR-TKIs target treatment for patients with NSCLC
    Wu, Xuan
    Liang, Wenhua
    Hou, Xue
    Lin, Zhong
    Zhao, Hongyun
    Huang, Yan
    Fang, Wenfeng
    Zhao, Yuanyuan
    Wu, Jingxun
    Yang, Yunpeng
    Xue, Chong
    Hu, Zhihuang
    Zhang, Jing
    Zhang, Jianwei
    Ma, Yuxiang
    Zhou, Ting
    Qin, Tao
    Zhang, Li
    ONCOTARGETS AND THERAPY, 2013, 6 : 1481 - 1491
  • [9] Beyond disease-progression: Clinical outcomes after EGFR-TKIs in a cohort of EGFR mutated NSCLC patients
    Tudor, Roxana Aline
    D'Silva, Adrijana
    Tremblay, Alain
    MacEachern, Paul
    Morris, Don
    Brenner, Darren
    Kopciuk, Karen
    Bebb, Dafydd Gwyn
    PLOS ONE, 2017, 12 (08):
  • [10] Clinical and molecular evidences of epithelial to mesenchymal transition in acquired resistance to EGFR-TKIs
    Chung, Jin-Haeng
    Rho, Jin Kyung
    Xu, Xianhua
    Lee, Jong Seok
    Yoon, Ho Il
    Lee, Choon Taek
    Choi, Yun Jung
    Kim, Hye-Ryoun
    Kim, Cheol Hyeon
    Lee, Jae Cheol
    LUNG CANCER, 2011, 73 (02) : 176 - 182