Brain metastases in patients with EGFR-mutated or ALK-rearranged non-small-cell lung cancers

被引:432
作者
Rangachari, Deepa [1 ]
Yamaguchi, Norihiro [1 ]
VanderLaan, Paul A. [2 ]
Folch, Erik [1 ,3 ]
Mahadevan, Anand [4 ]
Floyd, Scott R. [4 ]
Uhlmann, Erik J. [5 ]
Wong, Eric T. [5 ]
Dahlberg, Suzanne E. [6 ,7 ]
Huberman, Mark S. [1 ]
Costa, Daniel B. [1 ]
机构
[1] Harvard Univ, Beth Israel Deaconess Med Ctr, Sch Med, Dept Med, Boston, MA 02215 USA
[2] Harvard Univ, Beth Israel Deaconess Med Ctr, Sch Med, Dept Pathol, Boston, MA 02215 USA
[3] Harvard Univ, Beth Israel Deaconess Med Ctr, Sch Med, Dept Surg, Boston, MA 02215 USA
[4] Harvard Univ, Beth Israel Deaconess Med Ctr, Sch Med, Dept Radiat Oncol, Boston, MA 02215 USA
[5] Harvard Univ, Beth Israel Deaconess Med Ctr, Sch Med, Dept Neurol, Boston, MA 02215 USA
[6] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Biostat & Computat Biol, Boston, MA 02115 USA
[7] Harvard Univ, Sch Med, Sch Publ Hlth, Boston, MA USA
基金
美国国家卫生研究院;
关键词
Lung cancer; NSCLC; Brain metastases; EGFR; ALK; Mutation; Rearrangement; Central nervous system; CNS; CHEMOTHERAPY; ERLOTINIB; SYSTEM; CRIZOTINIB; MUTATIONS; GEFITINIB;
D O I
10.1016/j.lungcan.2015.01.020
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: Brain metastases (BM) are common in non-small-cell lung cancer (NSCLC). However, the baseline incidence and evolution of BM over time in oncogene-driven NSCLCs are seldom reported. In this study, we evaluated the frequency of BM in patients with epidermal growth factor receptor (EGFR)-mutated or anaplastic lymphoma kinase (ALK)-rearranged NSCLC. Methods: The presence of BM, clinicopathologic data, and tumor genotype were retrospectively compiled and analyzed from a cohort of 381 patients. Results: We identified 86 EGFR-mutated (90.7% with metastatic disease; 85.9% received an EGFR inhibitor) and 23 ALK-rearranged (91.3% with metastatic disease; 85.7% received an ALK inhibitor) NSCLCs. BM were present in 24.4% of EGFR-mutated and 23.8% of ALK-rearranged NSCLCs at the time of diagnosis of advanced disease. This study did not demonstrate a difference in the cumulative incidence of BM over time between the two cohorts (EGFR/ALK cohort competing risk regression [CRR] coefficient of 0.78[95% CI 0.44-1.39], p= 0.41). In still living patients with advanced EGFR-mutated NSCLC, 34.2% had BM at 1 year, 38.4% at 2 years, 46.7% at 3 years, 48.7% at 4 years, and 52.9% at 5 years. In still living patients with advanced ALK-rearranged NSCLC, 23.8% had BM at 1 year, 45.5% at 2 years, and 58.4% at 3 years. Conclusions: BM are frequent in advanced EGFR-mutated or ALK-rearranged NSCLCs, with an estimated >45% of patients with CNS involvement by three years of survival with the use of targeted therapies. These data point toward the CNS as an important unmet clinical need in the evolving schema for personalized care in NSCLC. (c) 2015 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:108 / 111
页数:4
相关论文
共 50 条
[31]   Response of Leptomeningeal Metastases in EGFR-Mutated Non-Small-Cell Lung Cancer to Afatinib in the Absence of Radiotherapy [J].
Llinas-Quintero, Nestor ;
Gonzalez-Hoyos, David ;
Yepes, Andres ;
Herrera, Diego A. ;
Pelaez-Arroyave, Sebastian ;
Caicedo-Zamudio, Carlos ;
Blanco-Daza, Erick ;
Cuello-Lopez, Javier .
CASE REPORTS IN ONCOLOGICAL MEDICINE, 2019, 2019
[32]   Treating patients with ALK-rearranged non-small-cell lung cancer: mechanisms of resistance and strategies to overcome it [J].
Drizou, M. ;
Kotteas, E. A. ;
Syrigos, N. .
CLINICAL & TRANSLATIONAL ONCOLOGY, 2017, 19 (06) :658-666
[33]   Efficacy of EGFR Tyrosine Kinase Inhibitors in Patients With EGFR-Mutated Non-Small-Cell Lung Cancer: A Meta-Analysis of 13 Randomized Trials [J].
Petrelli, Fausto ;
Borgonovo, Karen ;
Cabiddu, Mary ;
Barni, Sandro .
CLINICAL LUNG CANCER, 2012, 13 (02) :107-114
[34]   Standard-Dose Osimertinib in EGFR-Mutated Non-Small-Cell Lung Adenocarcinoma With Leptomeningeal Disease [J].
McLean, Luke S. ;
Faisal, Wasek ;
Parakh, Sagun ;
Kao, Steven C. ;
Lewis, Craig R. ;
Chin, Melvin T. ;
Voskoboynik, Mark ;
Itchins, Malinda J. ;
Jennens, Ross R. ;
Broad, Adam R. ;
Morris, Tessa A. ;
Solomon, Benjamin J. .
JCO PRECISION ONCOLOGY, 2021, 5 :561-568
[35]   Genetic landscape of patients with ALK-rearranged non-small-cell lung cancer (NSCLC) and response to ceritinib in ASCEND-1 study [J].
Tan, D. S-W. ;
Thomas, M. ;
Kim, D-W. ;
Szpakowski, S. ;
Urban, P. ;
Mehra, R. ;
Chow, L. Q. M. ;
Sharma, S. ;
Solomon, B. J. ;
Felip, E. ;
Camidge, D. R. ;
Vansteenkiste, J. ;
Petruzzelli, L. ;
Pantano, S. ;
Shaw, A. T. .
LUNG CANCER, 2022, 163 :7-13
[36]   Imaging Features and Metastatic Patterns of Advanced ALK-Rearranged Non-Small Cell Lung Cancer [J].
Mendoza, Dexter P. ;
Lin, Jessica J. ;
Rooney, Marguerite M. ;
Chen, Tianqi ;
Sequist, Lecia V. ;
Shaw, Alice T. ;
Digumarthy, Subba R. .
AMERICAN JOURNAL OF ROENTGENOLOGY, 2020, 214 (04) :766-774
[37]   Non-small-cell lung cancer: how to manage EGFR-mutated disease [J].
Pecci, Federica ;
Cantini, Luca ;
Metro, Giulio ;
Ricciuti, Biagio ;
Lamberti, Giuseppe ;
Farooqi, Ammad Ahmad ;
Berardi, Rossana .
DRUGS IN CONTEXT, 2022, 11
[38]   Monomerization of ALK Fusion Proteins as a Therapeutic Strategy in ALK-Rearranged Non-small Cell Lung Cancers [J].
Hirai, Noriko ;
Sasaki, Takaaki ;
Okumura, Shunsuke ;
Minami, Yoshinori ;
Chiba, Shinichi ;
Ohsaki, Yoshinobu .
FRONTIERS IN ONCOLOGY, 2020, 10
[39]   Meta-analysis of Targeted Therapies in EGFR-mutated Non-Small Cell Lung Cancer [J].
Qureshi, Zaheer ;
Altaf, Faryal ;
Jamil, Abdur ;
Siddique, Rimsha .
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 2025, 48 (01) :44-54
[40]   Predictive factors for EGFR-tyrosine kinase inhibitor retreatment in patients with EGFR-mutated non-small-cell lung cancer - A multicenter retrospective SEQUENCE study [J].
Chang, Gee-Chen ;
Tseng, Chien-Hua ;
Hsu, Kuo-Hsuan ;
Yu, Chong-Jen ;
Yang, Cheng-Ta ;
Chen, Kun-Chieh ;
Yang, Tsung-Ying ;
Tseng, Jeng-Sen ;
Liu, Chien-Ying ;
Liao, Wei-Yu ;
Hsia, Te-Chun ;
Tu, Chih-Yen ;
Lin, Meng-Chih ;
Tsai, Ying-Huang ;
Hsieh, Meng-Jer ;
Wu, Wen-Shuo ;
Chen, Yuh-Min .
LUNG CANCER, 2017, 104 :58-64