Continuation of gefitinib beyond progression in patients with EGFR mutation-positive non-small-cell lung cancer: A phase II single-arm trial

被引:13
|
作者
Lim, Sung Won [1 ]
Park, Sehhoon [1 ]
Kim, Youjin [1 ]
Cho, Jang Ho [1 ]
Park, Song Ee [1 ]
Lee, Hansang [1 ]
Kim, Hee Kyung [1 ]
Kim, Sung Min [2 ]
Sun, Jong Mu [1 ]
Lee, Se-Hoon [1 ]
Ahn, Jin Seok [1 ]
Park, Keunchil [1 ]
Ahn, Myung-Ju [1 ]
机构
[1] Sungkyunkwan Univ, Samsung Med Ctr, Dept Med, Div Hematol Oncol,Sch Med, Seoul, South Korea
[2] Sungkyunkwan Univ, Samsung Changwon Med Ctr, Sch Med, Seoul, South Korea
关键词
Gefitinib; Non-small cell lung cancer; EGFR mutation; GROWTH-FACTOR RECEPTOR; ACQUIRED-RESISTANCE; ASIAN PATIENTS; DISEASE FLARE; ERLOTINIB; DISCONTINUATION; AFATINIB;
D O I
10.1016/j.lungcan.2018.08.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives: Several studies have demonstrated the promise of continuation of epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI) beyond progression in patients with EGFR-mutant non-small-cell lung cancer (NSCLC). The aim of the present study is to clarify the efficacy of continuation of gefitinib in patients with NSCLC beyond progression. Materials and methods: A total of 50 patients with EGFR-mutant NSCLC who progressed based on Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 criteria during gefitinib treatment were eligible. The primary endpoint was progression-free survival-2 (PFS2; time from first gefitinib dose to off-gefitinib progression). Secondary endpoints were PFS1 (time from first gefitinib dose to RECIST 1.1 progression); the difference between PFS2 and PFS1 (PFS2-PFS1); overall survival (OS); and safety. Patients received gefitinib 250 mg/d orally until symptomatic progression or at the investigator's discretion. Results: Between January 2016 and March 2017, 50 patients were enrolled in this study. One patient withdrew consent, leaving a total of 49 patients to be evaluated. The median PFS2-PFS1 was 5.1 months (95% CI, 2.5-7.8), and the median PFS2 was 27.7 months (95% CI, 21.6-33.9). Twelve patients (24.4%) continued gefitinib therapy for 14 months (median value, range 7.2-20.3 months) after RECIST 1.1 progression. The median OS was not reached. Patients were classified by the characteristics of progression at the time of enrollment. PFS2-PFS1 was significantly shorter in patients with pleural metastasis or pleural effusion compared with the other types of progression (1.8 months vs. 7.1 months, p-value = 0.005). Conclusion: In patients with EGFR-mutant NSCLC who experience progression, it is beneficial to maintain gefitinib treatment with local treatment such as radiotherapy until symptomatic progression. However, in patients with pleural metastasis or effusion, continuation of gefitinib beyond progression should be carefully determined on a case by case basis.
引用
收藏
页码:293 / 297
页数:5
相关论文
共 50 条
  • [41] Erlotinib and bevacizumab in patients with advanced non-small-cell lung cancer and activating EGFR mutations (BELIEF): an international, multicentre, single-arm, phase 2 trial
    Rosell, Rafael
    Dafni, Urania
    Felip, Enriqueta
    Curioni-Fontecedro, Alessandra
    Gautschi, Oliver
    Peters, Solange
    Massuti, Bartomeu
    Palmero, Ramon
    Ponce Aix, Santiago
    Carcereny, Enric
    Frueh, Martin
    Pless, Miklos
    Popat, Sanjay
    Kotsakis, Athanasios
    Cuffe, Sinead
    Bidoli, Paolo
    Favaretto, Adolfo
    Froesch, Patrizia
    Reguart, Noemi
    Puente, Javier
    Coate, Linda
    Barlesi, Fabrice
    Rauch, Daniel
    Thomas, Michael
    Camps, Carlos
    Gomez-Codina, Jose
    Majem, Margarita
    Porta, Rut
    Shah, Riyaz
    Hanrahan, Emer
    Kammler, Roswitha
    Ruepp, Barbara
    Rabaglio, Manuela
    Kassapian, Marie
    Karachaliou, Niki
    Tam, Rachel
    Shames, David S.
    Molina-Vila, Miguel A.
    Stahel, Rolf A.
    LANCET RESPIRATORY MEDICINE, 2017, 5 (05): : 435 - 444
  • [42] Current and Emerging Options in the Management of EGFR Mutation-Positive Non-Small-Cell Lung Cancer: Considerations in the Elderly
    Gabriele Minuti
    Armida D’Incecco
    Federico Cappuzzo
    Drugs & Aging, 2015, 32 : 907 - 916
  • [43] Osimertinib As First-Line Treatment of EGFR Mutation-Positive Advanced Non-Small-Cell Lung Cancer
    Ramalingam, Suresh S.
    Yang, James C-H
    Lee, Chee Khoon
    Kurata, Takayasu
    Kim, Dong-Wan
    John, Thomas
    Nogami, Naoyuki
    Ohe, Yuichiro
    Mann, Helen
    Rukazenkov, Yuri
    Ghiorghiu, Serban
    Stetson, Daniel
    Markovets, Aleksandra
    Barrett, J. Carl
    Thress, Kenneth S.
    Janne, Pasi A.
    JOURNAL OF CLINICAL ONCOLOGY, 2018, 36 (09) : 841 - +
  • [44] OVERCOMING ERLOTINIB RESISTANCE IN EGFR MUTATION-POSITIVE NON-SMALL-CELL LUNG CANCER CELLS BY TARGETING SURVIVIN
    Okamoto, K.
    Okamoto, I.
    Hatashita, E.
    Kuwata, K.
    Yamaguchi, H.
    Kita, A.
    Yamanaka, K.
    Ono, M.
    Nakagawa, K.
    ANNALS OF ONCOLOGY, 2012, 23 : 85 - 85
  • [45] Tyrosine Kinase Inhibitors for the Treatment of EGFR Mutation-Positive Non-Small-Cell Lung Cancer: A Clash of the Generations
    Shah, Riyaz
    Lester, Jason F.
    CLINICAL LUNG CANCER, 2020, 21 (03) : E216 - E228
  • [46] Effects of dose modifications on the safety and efficacy of dacomitinib for EGFR mutation-positive non-small-cell lung cancer
    Corral, Jesus
    Mok, Tony S.
    Nakagawa, Kazuhiko
    Rosell, Rafael
    Lee, Ki Hyeong
    Migliorino, Maria Rita
    Pluzanski, Adam
    Linke, Rolf
    Devgan, Geeta
    Tan, Weiwei
    Quinn, Susan
    Wang, Tao
    Wu, Yi-Long
    FUTURE ONCOLOGY, 2019, 15 (24) : 2795 - 2805
  • [47] Phase 1 study of DS-1205c combined with gefitinib for EGFR mutation-positive non-small cell lung cancer
    Goto, Koichi
    Shiraishi, Yoshimasa
    Murakami, Haruyasu
    Horinouchi, Hidehito
    Toyozawa, Ryo
    Takeda, Masayuki
    Uno, Makiko
    Crawford, Nigel
    McGill, Joseph
    Jimbo, Takeshi
    Ishigami, Masato
    Takayama, Gensuke
    Nakayama, Shintaro
    Ohwada, Shoichi
    Nishio, Makoto
    CANCER MEDICINE, 2023, 12 (06): : 7090 - 7104
  • [48] Current and Emerging Options in the Management of EGFR Mutation-Positive Non-Small-Cell Lung Cancer: Considerations in the Elderly
    Minuti, Gabriele
    D'Incecco, Armida
    Cappuzzo, Federico
    DRUGS & AGING, 2015, 32 (11) : 907 - 916
  • [49] Optimizing outcomes and treatment sequences in EGFR mutation-positive non-small-cell lung cancer: recent updates
    Girard, Nicolas
    FUTURE ONCOLOGY, 2019, 15 (25) : 2983 - 2997
  • [50] First- and second-line treatment of non-small-cell lung cancer patients with EGFR mutation-positive tumors
    Reck, Martin
    Reinmuth, Niels
    Heigener, David F.
    LUNG CANCER MANAGEMENT, 2012, 1 (03) : 201 - 217