Comprehensive Genomic Profiling Identifies a Subset of Crizotinib-Responsive ALK-Rearranged Non-Small Cell Lung Cancer Not Detected by Fluorescence In Situ Hybridization

被引:95
|
作者
Ali, Siraj M. [1 ]
Hensing, Thomas [2 ,4 ]
Schrock, Alexa B. [1 ]
Allen, Justin [1 ]
Sanford, Eric [1 ]
Gowen, Kyle [1 ]
Kulkarni, Atul [6 ]
He, Jie [1 ]
Suh, James H. [1 ]
Lipson, Doron [1 ]
Elvin, Julia A. [1 ]
Yelensky, Roman [1 ]
Chalmers, Zachary [1 ]
Chmielecki, Juliann [1 ]
Peled, Nir [7 ]
Klempner, Samuel J. [8 ]
Firozvi, Kashif [9 ]
Frampton, Garrett M. [1 ]
Molina, Julian R. [10 ]
Menon, Smitha [11 ]
Brahmer, Julie R. [12 ]
MacMahon, Heber [5 ]
Nowak, Jan [3 ]
Ou, Sai-Hong Ignatius [8 ]
Zauderer, Marjorie [13 ]
Ladanyi, Marc [13 ]
Zakowski, Maureen [13 ]
Fischbach, Neil [14 ]
Ross, Jeffrey S. [1 ,15 ]
Stephens, Phil J. [1 ]
Miller, Vincent A. [1 ]
Wakelee, Heather [16 ]
Ganesan, Shridar [6 ]
Salgia, Ravi [4 ]
机构
[1] Fdn Med Inc, Cambridge, MA USA
[2] North Shore Univ Hlth Syst, Dept Med, Evanston, IL USA
[3] North Shore Univ Hlth Syst, Dept Pathol, Evanston, IL USA
[4] Univ Chicago, Dept Med, 5841 S Maryland Ave, Chicago, IL 60637 USA
[5] Univ Chicago, Dept Radiol, Chicago, IL 60637 USA
[6] Canc Inst New Jersey, New Brunswick, NJ USA
[7] Davidoff Canc Ctr, Tiqwa, Israel
[8] Univ Calif Irvine, Sch Med, Chao Family Comprehens Canc Ctr, Irvine, CA 92717 USA
[9] Maryland Hematol Oncol, Wheaton, IL USA
[10] Mayo Clin, Rochester, MN USA
[11] Froedtert Canc Ctr, Milwaukee, WI USA
[12] Johns Hopkins Med Inst, Kimmel Comprehens Canc Ctr, Baltimore, MD 21205 USA
[13] Mem Sloan Kettering Canc Ctr, Manhattan, KS USA
[14] Bridgeport Oncol, Bridgeport, CT USA
[15] Albany Med Coll, Albany, NY 12208 USA
[16] Stanford Univ, Dept Med, Sch Med, Div Oncol, Stanford, CA 94305 USA
来源
ONCOLOGIST | 2016年 / 21卷 / 06期
关键词
ALK; Crizotinib; Fluorescence in situ hybridization; Genomic profiling; Fusion; FUSION VARIANT; HIP1-ALK; ADENOCARCINOMAS; CHEMOTHERAPY; RESISTANCE; NSCLC;
D O I
10.1634/theoncologist.2015-0497
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction. For patients with non-small cell lung cancer (NSCLC) to benefit from ALK inhibitors, sensitive and specific detection of ALK genomic rearrangements is needed. ALK break-apart fluorescence in situ hybridization (FISH) is the U.S. Food and Drug Administration approved and standard-of-care diagnostic assay, but identification of ALK rearrangements by other methods reported in NSCLC cases that tested negative for ALK rearrangements by FISH suggests a significant false-negative rate. We report here a large series of NSCLC cases assayed by hybrid-capture-based comprehensive genomic profiling (CGP) in the course of clinical care. Materials and Methods. Hybrid-capture-based CGP using next-generation sequencing was performed in the course of clinical care of 1,070 patients with advanced lung cancer. Each tumor sample was evaluated for all classes of genomic alterations, including base-pair substitutions, insertions/deletions, copy number alterations and rearrangements, as well as fusions/rearrangements. Results. A total of 47 patients (4.4%) were found to harbor ALK rearrangements, of whom 41 had an EML4-ALK fusion, and 6 had other fusion partners, including 3 previously unreported rearrangement events: EIF2AK-ALK, PPM1B-ALK, and PRKAR1A-ALK. Of 41 patients harboring ALK rearrangements, 31 had prior FISH testing results available. Of these, 20 were ALK FISH positive, and 11 (35%) were ALK FISH negative. Of the latter 11 patients, 9 received crizotinib based on the CGP results, and 7 achieved a response with median duration of 17 months. Conclusion. Comprehensive genomic profiling detected canonical ALK rearrangements and ALK rearrangements with noncanonical fusion partners in a subset of patients with NSCLC with previously negative ALK FISH results. In this series, such patients had durable responses to ALK inhibitors, comparable to historical response rates for ALK FISH-positive cases.
引用
收藏
页码:762 / 770
页数:9
相关论文
共 50 条
  • [41] ALK-rearranged non-small cell lung cancer is associated with a high rate of venous thromboembolism
    Zer, A.
    Hershko-Klement, A.
    Hwang, D.
    Korpanty, G.
    Leighl, N.
    Liu, G.
    Feld, R.
    Burkes, R.
    Tsao, M.
    Shepherd, F.
    JOURNAL OF THORACIC ONCOLOGY, 2016, 11 (04) : S134 - S134
  • [42] Alectinib: A Review of Its Use in Advanced ALK-Rearranged Non-Small Cell Lung Cancer
    McKeage, Kate
    DRUGS, 2015, 75 (01) : 75 - 82
  • [43] Treatment of ALK-Rearranged Non-Small Cell Lung Cancer: Recent Progress and Future Directions
    Cameron, Laird
    Solomon, Benjamin
    DRUGS, 2015, 75 (10) : 1059 - 1070
  • [44] Immunotherapy for ALK-Rearranged Non-Small Cell Lung Cancer: Challenges Inform Promising Approaches
    Sankar, Kamya
    Nagrath, Sunitha
    Ramnath, Nithya
    CANCERS, 2021, 13 (06)
  • [45] Ceritinib (LDK378): A Potent Alternative to Crizotinib for ALK-Rearranged Non-Small-Cell Lung Cancer
    Li, Sen
    Qi, Xiaolong
    Huang, Yufeng
    Liu, Dingfeng
    Zhou, Fangyu
    Zhou, Caicun
    CLINICAL LUNG CANCER, 2015, 16 (02) : 86 - 91
  • [46] 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
    JOURNAL OF CLINICAL ONCOLOGY, 2015, 33 (17) : 1881 - 1888
  • [47] ALK immunohistochemistry scores do not predict sensitivity to crizotinib in fluorescence in situ hybridization-positive non-small cell lung cancer patients
    Metro, G.
    Chiari, R.
    Giannarelli, D.
    Sidoni, A.
    Bellezza, G.
    JOURNAL OF THORACIC ONCOLOGY, 2018, 13 (04) : S14 - S15
  • [48] Targeting ALK-rearranged non-small-cell lung cancer: an update
    Sullivan, Ivana
    Planchard, David
    FUTURE ONCOLOGY, 2017, 13 (14) : 1213 - 1217
  • [49] The analysis of ALK gene rearrangement by fluorescence in situ hybridization in non-small cell lung cancer patients
    Wojas-Krawczyk, Kamila
    Krawczyk, Pawel Adam
    Ramlau, Rodryg Adam
    Szumilo, Justyna
    Kozielski, Jerzy
    Kalinka-Warzochas, Ewa
    Bryl, Maciej
    Knopik-Nabrowicz, Alina
    Spychalski, Lukasz
    Szczesna, Aleksandra
    Rydzik, Ewelina
    Milanowski, Janusz
    WSPOLCZESNA ONKOLOGIA-CONTEMPORARY ONCOLOGY, 2013, 17 (06): : 484 - 492
  • [50] Clinical features and outcomes of ALK rearranged non-small cell lung cancer with primary resistance to crizotinib
    Ma, Di
    Zhang, Yan
    Xing, Puyuan
    Hao, Xuezhi
    Wang, Mengzhao
    Wang, Yan
    Shan, Li
    Xin, Tao
    Liang, Hongge
    Du, Yang
    Zhang, Zhaohui
    Liang, Li
    Li, Junling
    THORACIC CANCER, 2019, 10 (05) : 1213 - 1219