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:96
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
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
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