How I treat ALK-positive non-small cell lung cancer

被引:38
作者
McCusker, Michael G. [1 ]
Russo, Alessandro [1 ,2 ,3 ]
Scilla, Katherine A. [1 ]
Mehra, Ranee [1 ]
Rolfo, Christian [1 ]
机构
[1] Univ Maryland, Greenebaum Comprehens Canc Ctr, Baltimore, MD 21201 USA
[2] Univ Messina, Med Oncol Unit AO Papardo, Messina, Italy
[3] Univ Messina, Dept Human Pathol, Messina, Italy
关键词
TYROSINE KINASE INHIBITORS; BRAIN METASTASES; OPEN-LABEL; CRIZOTINIB; CHEMOTHERAPY; RESISTANCE; CERITINIB; ALECTINIB; THERAPY;
D O I
10.1136/esmoopen-2019-000524
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Since the discovery of anaplastic lymphocyte kinase (ALK) rearrangement in non-small cell lung cancer (NSCLC) and subsequent development of increasingly effective and central nervous system (CNS)-penetrant first-generation, second-generation and third-generation ALK tyrosine kinase inhibitors (TKIs), the landscape of resistance mechanisms and treatment decisions has become increasingly complex. Tissue and/or plasma-based molecular tests can identify not only the rearrangement proper but also common resistance mechanisms to guide decision-making for further lines of treatment. However, frequently encountered questions exist regarding how to diagnosis ALK rearrangement, how to select a first-line ALK TKI, how to diagnose and manage ALK TKI resistance, how to control CNS disease and how to handle failure of ALK inhibition. Herein, we attempt to answer these questions through the evidence-based interpretation of studies on ALK-rearranged NSCLC combined with experience gained from our institution. The authors also propose a therapeutic algorithm for the management of this complex and highly treatable disease to assist clinicians globally in the treatment of patients with ALK-positive NSCLC.
引用
收藏
页数:6
相关论文
共 36 条
  • [1] Determinants of high tumor mutational burden (TMB) and mutational signatures in breast cancer
    Barroso-Sousa, Romualdo
    Jain, Esha
    Kim, Dewey
    Partridge, Ann H.
    Cohen, Ofir
    Wagle, Nikhil
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2018, 36 (15)
  • [2] Brigatinib versus Crizotinib in ALK-Positive Non-Small-Cell Lung Cancer
    Camidge, D. R.
    Kim, H. R.
    Ahn, M. -J.
    Yang, J. C. -H.
    Han, J. -Y.
    Lee, J. -S.
    Hochmair, M. J.
    Li, J. Y. -C.
    Chang, G. -C.
    Lee, K. H.
    Gridelli, C.
    Delmonte, A.
    Garcia Campelo, R.
    Kim, D. -W.
    Bearz, A.
    Griesinger, F.
    Morabito, A.
    Felip, E.
    Califano, R.
    Ghosh, S.
    Spira, A.
    Gettinger, S. N.
    Tiseo, M.
    Gupta, N.
    Haney, J.
    Kerstein, D.
    Popat, S.
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2018, 379 (21) : 2027 - 2039
  • [3] Camidge DR, 2019, J THORAC ONCOL, P30210
  • [4] Molecular Mechanism Behind the Resistance of the G1202R-Mutated Anaplastic Lymphoma Kinase to the Approved Drug Ceritinib
    Chen, Chaohong
    He, Zhifeng
    Xie, Deyao
    Zheng, Liangcheng
    Zhao, Tianhao
    Zhang, Xinbo
    Cheng, Dezhi
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 2018, 122 (17) : 4680 - 4692
  • [5] Prevalence and natural history of ALK positive non-small-cell lung cancer and the clinical impact of targeted therapy with ALK inhibitors
    Chia, Puey Ling
    Mitchell, Paul
    Dobrovic, Alexander
    John, Thomas
    [J]. CLINICAL EPIDEMIOLOGY, 2014, 6 : 423 - 432
  • [6] ASCEND-8: A Randomized Phase 1 Study of Ceritinib, 450 mg or 600 mg, Taken with a Low-Fat Meal versus 750 mg in Fasted State in Patients with Anaplastic Lymphoma Kinase (ALK)-Rearranged Metastatic Non-Small Cell Lung Cancer (NSCLC)
    Cho, Byoung Chul
    Kim, Dong-Wan
    Bearz, Alessandra
    Laurie, Scott A.
    McKeage, Mark
    Borra, Gloria
    Park, Keunchil
    Kim, Sang-We
    Ghosn, Marwan
    Ardizzoni, Andrea
    Maiello, Evaristo
    Greystoke, Alastair
    Yu, Richard
    Osborne, Karen
    Gu, Wen
    Scott, Jeffrey W.
    Passos, Vanessa Q.
    Lau, Yvonne Y.
    Wrona, Anna
    [J]. JOURNAL OF THORACIC ONCOLOGY, 2017, 12 (09) : 1357 - 1367
  • [7] Clinical Experience With Crizotinib in Patients With Advanced ALK-Rearranged Non-Small-Cell Lung Cancer and Brain Metastases
    Costa, Daniel B.
    Shaw, Alice T.
    Ou, Sai-Hong I.
    Solomon, Benjamin J.
    Riely, Gregory J.
    Ahn, Myung-Ju
    Zhou, Caicun
    Shreeve, S. Martin
    Selaru, Paulina
    Polli, Anna
    Schnell, Patrick
    Wilner, Keith D.
    Wiltshire, Robin
    Camidge, D. Ross
    Crino, Lucio
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2015, 33 (17) : 1881 - 1888
  • [8] CSF Concentration of the Anaplastic Lymphoma Kinase Inhibitor Crizotinib
    Costa, Daniel B.
    Kobayashi, Susumu
    Pandya, Shuchi S.
    Yeo, Wee-Lee
    Shen, Zhongzhou
    Tan, Weiwei
    Wilner, Keith D.
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2011, 29 (15) : E443 - E445
  • [9] Epithelial-to-Mesenchymal Transition Is a Mechanism of ALK Inhibitor Resistance in Lung Cancer Independent of ALK Mutation Status
    Fukuda, Koji
    Takeuchi, Shinji
    Arai, Sachiko
    Katayama, Ryohei
    Nanjo, Shigeki
    Tanimoto, Azusa
    Nishiyama, Akihiro
    Nakagawa, Takayuki
    Taniguchi, Hirokazu
    Suzuki, Takeshi
    Yamada, Tadaaki
    Nishihara, Hiroshi
    Ninomiya, Hironori
    Ishikawa, Yuichi
    Baba, Satoko
    Takeuchi, Kengo
    Horiike, Atsushi
    Yanagitani, Noriko
    Nishio, Makoto
    Yano, Seiji
    [J]. CANCER RESEARCH, 2019, 79 (07) : 1658 - 1670
  • [10] Alectinib versus crizotinib in treatment-naive anaplastic lymphoma kinase-positive (ALK plus ) non-small-cell lung cancer: CNS efficacy results from the ALEX study
    Gadgeel, S.
    Peters, S.
    Mok, T.
    Shaw, A. T.
    Kim, D. W.
    Ou, S. I.
    Perol, M.
    Wrona, A.
    Novello, S.
    Rosell, R.
    Zeaiter, A.
    Liu, T.
    Nuesch, E.
    Balas, B.
    Camidge, D. R.
    [J]. ANNALS OF ONCOLOGY, 2018, 29 (11) : 2214 - 2222