EGFR tyrosine kinase inhibitors beyond focal progression obtain a prolonged disease control in patients with advanced adenocarcinoma of the lung

被引:40
作者
Conforti, Fabio [1 ]
Catania, Chiara [1 ]
Toffalorio, Francesca [1 ]
Duca, Matteo [1 ]
Spitaleri, Gianluca [1 ]
Barberis, Massimo [2 ]
Noberasco, Cristina [1 ]
Delmonte, Angelo [1 ]
Santarpia, Mariacarmela [1 ]
Lazzari, Chiara [1 ]
De Pas, Tommaso Martino [1 ]
机构
[1] European Inst Oncol, Dept Med Oncol, Div New Drug Dev & Clin Pharmacol, Thorac & Sarcoma Oncol Unit, Milan, Italy
[2] European Inst Oncol, Div Pathol, Milan, Italy
关键词
Lung adenocarcinoma; TKI therapy; Beyond progression; Erlotinib; Gefitinib; Radiotherapy; Advanced lung adenocarcinoma; GASTROINTESTINAL STROMAL TUMORS; ADVANCED BREAST-CANCER; GEFITINIB FAILURE; ACQUIRED-RESISTANCE; 1ST-LINE TREATMENT; SALVAGE TREATMENT; ASIAN PATIENTS; OPEN-LABEL; PHASE-II; ERLOTINIB;
D O I
10.1016/j.lungcan.2013.05.019
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: Recent data show that EGFR pathway and its inhibition maintain their role after progression of disease during EGFR TKI therapy in NSCLCs. We conducted a retrospective study with the aim of evaluating efficacy and feasibility of prosecution of EGFR TKI therapy beyond focal progression associated to locoregional radiotherapy. Methods: We retrospectively analyzed the data of all NSCLC patients treated with EGFR TKIs in our institution from 2004 to 2012. We included in the analysis patients that after a focal disease progression, meant as a single lesion RECIST progression, have been treated with definitive locoregional radiotherapy, associated to continuation of EGFR TKI therapy until further progression. Results: 15 out of 147 patients (10%) satisfied inclusion criteria. The median progression free survival, measured from the date of focal progression until further progression of disease or death by any cause, was 10,9 months (range 3-32 months). The corresponding 6 and 12 months PFS rates were 73% and 33%, respectively. Conclusion: The longer disease control observed in our patients suggests that continuation of EGFR TKI beyond focal progression associated to a locoregional treatment is an efficacious therapeutic strategy. (C) 2013 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:440 / 444
页数:5
相关论文
共 36 条
[1]   Focal progression in patients with gastrointestinal stromal tumors after initial response to imatinib mesylate:: a three-center-based study of 38 patients [J].
Al-Batran, Salah-Eddin ;
Hartmann, Joerg Thomas ;
Heidel, Florian ;
Stoehlmacher, Jan ;
Wardelmann, Eva ;
Dechow, Claudius ;
Duex, Markus ;
Izbicki, Jacob Robert ;
Kraus, Thomas ;
Fischer, Thomas ;
Jaeger, Elke .
GASTRIC CANCER, 2007, 10 (03) :145-152
[2]   Duration of prior gefitinib treatment predicts survival potential in patients with lung adenocarcinoma receiving subsequent erlotinib [J].
Asami, Kazuhiro ;
Kawahara, Masaaki ;
Atagi, Shinji ;
Kawaguchi, Tomoya ;
Okishio, Kyoichi .
LUNG CANCER, 2011, 73 (02) :211-216
[3]   Capecitabine and trastuzumab in heavily pretreated metastatic breast cancer [J].
Bartsch, Rupert ;
Wenzel, Catharina ;
Altorjai, Gabriela ;
Pluschnig, Ursula ;
Rudas, Margaretha ;
Mader, Robert M. ;
Gnant, Michael ;
Zielinski, Christoph C. ;
Steger, Guenther G. .
JOURNAL OF CLINICAL ONCOLOGY, 2007, 25 (25) :3853-3858
[4]   Treatment of nonsmall cell lung cancer: overcoming the resistance to epidermal growth factor receptor inhibitors [J].
Carter, Corey A. ;
Giaccone, Giuseppe .
CURRENT OPINION IN ONCOLOGY, 2012, 24 (02) :123-129
[5]   Disease Flare after Tyrosine Kinase Inhibitor Discontinuation in Patients with EGFR-Mutant Lung Cancer and Acquired Resistance to Erlotinib or Gefitinib: Implications for Clinical Trial Design [J].
Chaft, Jamie E. ;
Oxnard, Geoffrey R. ;
Sima, Camelia S. ;
Kris, Mark G. ;
Miller, Vincent A. ;
Riely, Gregory J. .
CLINICAL CANCER RESEARCH, 2011, 17 (19) :6298-6303
[6]   Phase II study of erlotinib in advanced non-small-cell lung cancer after failure of gefitinib [J].
Cho, Byoung Chul ;
Im, Chong-Kun ;
Park, Moo-Suk ;
Kim, Se Kyu ;
Chang, Joon ;
Park, Jong Pil ;
Choi, Hye Jin ;
Kim, Yu Jin ;
Shin, Sang-Joon ;
Sohn, Joo Hyuk ;
Kim, Hoguen ;
Kim, Joo Hang .
JOURNAL OF CLINICAL ONCOLOGY, 2007, 25 (18) :2528-2533
[7]   Effects of Erlotinib in EGFR Mutated Non-Small Cell Lung Cancers with Resistance to Gefitinib [J].
Costa, Daniel B. ;
Nguyen, Kim-Son H. ;
Cho, Young C. ;
Sequist, Lecia V. ;
Jackman, David M. ;
Riely, GregoryJ. ;
Yeap, Beow Y. ;
Halmos, Balazs ;
Kim, Joo H. ;
Jaenne, Pasi A. ;
Huberman, Mark S. ;
Pao, William ;
Tenen, Daniel G. ;
Kobayashi, Susumu .
CLINICAL CANCER RESEARCH, 2008, 14 (21) :7060-7067
[8]   EGFR gene copy number as a predictive biomarker for patients receiving tyrosine kinase inhibitor treatment: a systematic review and meta-analysis in non-small-cell lung cancer [J].
Dahabreh, I. J. ;
Linardou, H. ;
Kosmidis, P. ;
Bafaloukos, D. ;
Murray, S. .
ANNALS OF ONCOLOGY, 2011, 22 (03) :545-552
[9]   Lapatinib plus capecitabine for HER2-positive advanced breast cancer [J].
Geyer, Charles E. ;
Forster, John ;
Lindquist, Deborah ;
Chan, Stephen ;
Romieu, C. Gilles ;
Pienkowski, Tadeusz ;
Jagiello-Gruszfeld, Agnieszka ;
Crown, John ;
Chan, Arlene ;
Kaufman, Bella ;
Skarlos, Dimosthenis ;
Campone, Mario ;
Davidson, Neville ;
Berger, Mark ;
Oliva, Cristina ;
Rubin, Stephen D. ;
Stein, Steven ;
Cameron, David .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 355 (26) :2733-2743
[10]   "Pulsatile" high-dose weekly erlotinib for CNS metastases from EGFR mutant non-small cell lung cancer [J].
Grommes, Christian ;
Oxnard, Geoffrey R. ;
Kris, Mark G. ;
Miller, Vincent A. ;
Pao, William ;
Holodny, Andrei I. ;
Clarke, Jennifer L. ;
Lassman, Andrew B. .
NEURO-ONCOLOGY, 2011, 13 (12) :1364-1369