Real Clinical Practice of Using Afatinib Therapy in NSCLC Patients with an Acquired EGFR T790M Mutation

被引:7
|
作者
Miyazaki, Kunihiko [1 ]
Tamura, Tomohiro [2 ]
Kaburagi, Takayuki [2 ]
Saito, Kazuhito [3 ,4 ]
Inagaki, Masaharu [3 ,4 ]
Yamashita, Takaaki [5 ]
Ichimura, Hideo [6 ,7 ]
Nawa, Takeshi [6 ,7 ]
Endo, Takeo [8 ]
Hayashihara, Kenji [9 ]
Kimura, Masaki [10 ]
Kurishima, Koichi [11 ]
Nakamura, Hiroyuki [12 ,13 ]
Furukawa, Kinya [12 ,13 ]
Kikuchi, Norihiro [14 ]
Satoh, Hiroaki [15 ]
Hizawa, Nobuyuki [16 ]
机构
[1] Ryugasaki Saiseikai Hosp, Div Resp Med, Ryugasaki, Japan
[2] Ibaraki Cent Hosp, Resp Ctr, Kasama, Ibaraki, Japan
[3] Tsuchiura Kyodo Gen Hosp, Div Resp Med, Tsuchiura, Ibaraki, Japan
[4] Tsuchiura Kyodo Gen Hosp, Div Thorac Surg, Tsuchiura, Ibaraki, Japan
[5] JA Toride Med Ctr, Div Resp Med, Toride, Japan
[6] Hitachi Gen Hosp, Div Resp Med, Hitachi, Ibaraki, Japan
[7] Hitachi Gen Hosp, Div Thorac Surg, Hitachi, Ibaraki, Japan
[8] Mito Med Ctr, Div Resp Med, Mito, Ibaraki, Japan
[9] Ibarakihigashi Hosp, Div Resp Med, Tokai, Ibaraki, Japan
[10] Tsukuba Mem Hosp, Div Thorac Surg, Tsukuba, Ibaraki, Japan
[11] Tsukuba Med Ctr Hosp, Div Resp Med, Tsukuba, Ibaraki, Japan
[12] Tokyo Med Univ, Div Resp Med, Ibaraki Med Ctr, Ami Machi, Tokyo, Japan
[13] Tokyo Med Univ, Div Thorac Surg, Ibaraki Med Ctr, Ami Machi, Tokyo, Japan
[14] Kasumigaura Med Ctr, Div Resp Med, Tsuchiura, Ibaraki, Japan
[15] Univ Tsukuba, Mito Med Ctr, Mito Kyodo Gen Hosp, Div Resp Med, Mito, Ibaraki, Japan
[16] Univ Tsukuba, Fac Clin Med, Tsukuba, Ibaraki, Japan
关键词
Clinical practice; afatinib; non-small cell lung cancer; acquired T790M mutation; osimertinib; immune-checkpoint inhibitor; CELL LUNG-CANCER; 1ST-LINE TREATMENT; OPEN-LABEL; GEFITINIB; ADENOCARCINOMA; OSIMERTINIB; EXPERIENCE; ERLOTINIB; RECEPTOR;
D O I
10.21873/anticanres.12871
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background/Aim: To describe real clinical outcomes when using afatinib therapy to treat non-small cell lung cancer patients who have an acquired EGFR T790M mutation. Materials and Methods: A retrospective chart review was conducted from January 2013 to November 2017 sourced from 15 medical institutes that cover a population of three million people. Results: There were 74 patients who met the above-mentioned criteria. Treatment outcomes with afatinib, in patients with or without tyrosine kinase inhibitor (TKI) therapy prior to afatinib, were similar to previously reported clinical trials. Stratification of patients by the presence or absence of TKI pretreatment before afatinib, and the presence or absence of an acquired T790M mutation found no statistical difference in overall survival. Conclusion: This population-based study found that the disadvantages of pretreatment before afatinib, and absence of an acquired T790M EGFR mutation, could be overcome by an appropriate treatment strategy in clinical practice.
引用
收藏
页码:5409 / 5415
页数:7
相关论文
共 50 条
  • [41] Afatinib increases sensitivity to radiation in non-small cell lung cancer cells with acquired EGFR T790M mutation
    Zhang, Shirong
    Zheng, Xiaoliang
    Huang, Haixiu
    Wu, Kan
    Wang, Bing
    Chen, Xufeng
    Ma, Shenglin
    ONCOTARGET, 2015, 6 (08) : 5832 - 5845
  • [42] The EGFR T790M Mutation in Acquired Resistance to an Irreversible Second-Generation EGFR Inhibitor
    Kim, Youngwook
    Ko, Jeonghun
    Cui, ZhengYun
    Abolhoda, Amir
    Ahn, Jin Seok
    Ou, Sai-Hong
    Ahn, Myung-Ju
    Park, Keunchil
    MOLECULAR CANCER THERAPEUTICS, 2012, 11 (03) : 784 - 791
  • [43] The EGFR T790M Mutation in Acquired Resistance to an Irreversible Second-Generation EGFR Inhibitor
    Kim, Youngwook
    Ko, Jeonghun
    Cui, Zhengyun
    Abolhoda, Amir
    Lee, Jeeyun
    Ahn, Jinseok
    Ou, Sai-Hong
    Ahn, Myung-Ju
    Park, Keunchil
    JOURNAL OF THORACIC ONCOLOGY, 2010, 5 (12) : S421 - S421
  • [44] Combined plasma and tissue genotyping of EGFR T790M benefits NSCLC patients: a real-world clinical example
    Wei, Bing
    Zhao, Chengzhi
    Li, Jun
    Zhao, Jiuzhou
    Ren, Pengfei
    Yang, Ke
    Yan, Chi
    Sun, Rui
    Ma, Jie
    Guo, Yongjun
    MOLECULAR ONCOLOGY, 2019, 13 (05) : 1226 - 1234
  • [45] KRAS and EGFR Amplifications Mediate Resistance to Rociletinib and Osimertinib in Acquired Afatinib-Resistant NSCLC Harboring Exon 19 Deletion/T790M in EGFR
    Nakatani, Kaori
    Yamaoka, Toshimitsu
    Ohba, Motoi
    Fujita, Ken-Ichi
    Arata, Satoru
    Kusumoto, Sojiro
    Taki-Takemoto, Iori
    Kamei, Daisuke
    Iwai, Shinichi
    Tsurutani, Junji
    Ohmori, Tohru
    MOLECULAR CANCER THERAPEUTICS, 2019, 18 (01) : 112 - 126
  • [46] Successful treatment with osimertinib for leptomeningeal carcinomatosis from NSCLC with the EGFR T790M mutation
    Yoshimura, Naruo
    Takahashi, Hidenori
    Kurosawa, Emiko
    Tanaka, Akiko
    Ebina, Masahito
    Ohrui, Takashi
    ANNALS OF ONCOLOGY, 2019, 30 : 139 - 139
  • [47] KRAS amplification mediates resistance to osimertinib in acquired afatinib-resistant NSCLC harboring exon 19 deletion/T790M in EGFR
    Yamaoka, Toshimitsu
    Motoi, Ohba
    Kishino, Yasunari
    Kusumoto, Sojiro
    Tsurutani, Junji
    Ohmori, Tohru
    CANCER RESEARCH, 2019, 79 (13)
  • [48] Acquired resistance of pulmonary adenocarcinoma to initially successful targeted therapy due to EGFR mutation T790M
    Jancarikova, D.
    Pesek, M.
    Benesova, L.
    Topolcan, O.
    Holubec, L., Jr.
    Minarik, M.
    ANTICANCER RESEARCH, 2007, 27 (4A) : 1879 - 1882
  • [49] Exploratory study on detecting EGFR mutation including T790M with blood samples from patients with NSCLC
    Kawamura, Takahisa
    Murakami, Haruyasu
    Kenmotsu, Hirotsugu
    CANCER SCIENCE, 2018, 109 : 1100 - 1100
  • [50] ROS1 Translocation as a Bystander Mutation in T790M EGFR Mutated NSCLC
    Stratmann, Jan
    Kriegsmann, Joerg
    Sulzbach, Bernd
    Thoeming, Bernd
    Serve, Hubert
    Sebastian, Martin
    JOURNAL OF THORACIC ONCOLOGY, 2017, 12 (01) : S1260 - S1260