Curative effect analysis of different treatments for gefitinib-resistance advanced non-small cell lung cancer patients

被引:0
|
作者
Shi, Hong [1 ]
Zhang, Xiaoyan [2 ]
Wang, Fei [3 ]
Liu, Daoming [1 ]
机构
[1] Taian City Cent Hosp, Dept Resp Med, Tai An 271000, Shandong, Peoples R China
[2] Taian City Cent Hosp, Dept Thorac Surg, Tai An 271000, Shandong, Peoples R China
[3] Taian City Cent Hosp, Dept Magnet Resonance Imaging, Tai An 271000, Shandong, Peoples R China
关键词
Non-small cell lung cancer; metastasis; chemotherapy; overall survival; gefitinib-resistance; progression-free survival; RECEPTOR TYROSINE KINASE; ACQUIRED-RESISTANCE; EGFR-TKI; ERLOTINIB; IRESSA; NSCLC; PLUS;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Objective: Gefitinib is effective epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKI) for advanced non-small cell lung cancer (NSCLC) patients, but with the drug use, inevitable gefitinib-resistance and severe complications were observed and resulted in failure treatments. The purpose of the present study was to investigate the curative effect of different treatment of navelbine plus cisplatin in combination with gefitinib and gefitinib single on gefitinib-resistance advanced NSCLC patients. Methods: Total Of 120 patients acquired gefitinib-resistance NSCLC patients treated in Taian City Central Hospital of Shandong province from May, 2010 to June, 2014 were incorporated in our study according to the inclusion and exclusion criteria. The patients were divided into chemotherapeutical group and gefitinib group and the mean follow-up was 12 months (6-39 months), the information of patients was recorded as gender, age, smoking, complications, hepatic metastasis, bone metastasis, brain metastasis and acquired chemotherapy or not. Chi-square test and t-test were performed to analyzed collection data, Log-rank was analyzed significance of survival time among groups and Cox regression was evaluated independent risk factors of survival analysis. Results: The survival time of chemotherapy group was significantly longer than gefitinib group; the survival time among the two groups was 29.06 and 15.23 months (P < 0.05), respectively. Multivariate Cox regression analyzed that lesion's metastasis (hepatic metastasis, bone metastasis and brain metastasis) and acquired chemotherapy were independent risk factors influence on patients overall survival time; gender, age, smoking, complications had no significance influence on survival time between the two groups. Conclusion: Lesion's metastasis and acquired chemotherapy were independent risk factors influence on patients' overall survival time and the survival time of chemotherapy group was significantly longer than gefitinib group.
引用
收藏
页码:16064 / 16070
页数:7
相关论文
共 50 条
  • [41] Drug resistance analysis of gefitinib-targeted therapy in non-small cell lung cancer
    Liu, Shuliang
    Yang, Hongji
    Ge, Xingping
    Su, Lingfei
    Zhang, Aifeng
    Liang, Liang
    ONCOLOGY LETTERS, 2016, 12 (05) : 3941 - 3943
  • [42] Gefitinib for Non-Small Cell Lung Cancer Patients with Liver Cirrhosis
    Kim, Young Hak
    Mio, Tadashi
    Mishima, Michiaki
    INTERNAL MEDICINE, 2009, 48 (18) : 1677 - 1679
  • [43] CLINICAL CHARACTERISTICS OF ACQUIRED RESISTANCE TO GEFITINIB IN NON-SMALL CELL LUNG CANCER
    Lee, Kye Young
    Kim, Hee Joung
    Kim, Young-Chul
    Shin, Kyeong-Cheol
    Lee, Jae Chol
    Ryu, Jeong Seon
    Jang, Seung Hoon
    Kim, Sun Young
    Jang, Tae Won
    RESPIROLOGY, 2010, 15 : 37 - 37
  • [44] Clinical Characteristics of Acquired Resistance to Gefitinib in Non-Small Cell Lung Cancer
    Lee, Kye Young
    Kim, Hee Joung
    Kim, Young-Chul
    Kim, Kyu-Sik
    Oh, In-Jae
    Ban, Hee Jung
    Lee, Sung Yong
    Jang, Tae Won
    Shin, Kyeong-Cheol
    Lee, Gwan Ho
    Lce, Jae Chol
    Ryu, Jeong-Seon
    Jang, Seung Hoon
    Lee, Jeong Eun
    Kim, Sun Young
    JOURNAL OF THORACIC ONCOLOGY, 2010, 5 (12) : S396 - S397
  • [45] Phase II Study of Gefitinib Readministration in Patients with Advanced Non-Small Cell Lung Cancer and Previous Response to Gefitinib
    Asahina, Hajime
    Oizumi, Satoshi
    Inoue, Akira
    Kinoshita, Ichiro
    Ishida, Takashi
    Fujita, Yuka
    Sukoh, Noriaki
    Harada, Masao
    Maemondo, Makoto
    Saijo, Yasuo
    Dosaka-Akita, Hirotoshi
    Isobe, Hiroshi
    Nukiwa, Toshihiro
    Nishimura, Masaharu
    ONCOLOGY, 2010, 79 (5-6) : 423 - 429
  • [46] Analysis of the response and toxicity to gefitinib of non-small cell lung cancer
    Konishi, J
    Yamazaki, K
    Kinoshita, I
    Isobe, H
    Ogura, S
    Sekine, S
    Ishida, T
    Takashima, R
    Nakadate, M
    Nishikawa, S
    Hattori, T
    Asahina, H
    Imura, M
    Kikuchi, E
    Kikuchi, J
    Shinagawa, N
    Yokouchi, H
    Munakata, M
    Dosaka-Akita, H
    Nishimura, M
    ANTICANCER RESEARCH, 2005, 25 (1B) : 435 - 441
  • [47] Overexpression of CTEN is associated with gefitinib resistance in non-small cell lung cancer
    Lu, Xiangdong
    Zhang, Yao
    Pan, Yukai
    Cao, Minmin
    Zhou, Xie
    Zhang, Tingrong
    ONCOLOGY LETTERS, 2021, 21 (01) : 1 - 8
  • [49] Amphiregulin induces resistance to gefitinib in non-small cell lung cancer cell lines
    Busser, Benoit
    Lucie, Sancey
    Marie, Favrot
    Luc, Coll Jean
    Amandine, Hurbin
    BULLETIN DU CANCER, 2009, 96 : S55 - S55
  • [50] Gefitinib therapy for non-small cell lung cancer
    Birnbaum A.
    Ready N.
    Current Treatment Options in Oncology, 2005, 6 (1) : 75 - 81