Genomic heterogeneity of ALK fusion breakpoints in non-small-cell lung cancer

Jason N. Rosenbaum, Ryan Bloom, Jason T. Forys, Jeff Hiken, Jon R. Armstrong, Julie Branson, Samantha McNulty, Priya D. Velu, Kymberlie Pepin, Haley Abel, Catherine E. Cottrell, John D. Pfeifer, Shashikant Kulkarni, Ramaswamy Govindan, Eric Q. Konnick, Christina M. Lockwood, Eric J. Duncavage

Research output: Contribution to journalArticlepeer-review

40 Scopus citations

Abstract

In lung adenocarcinoma, canonical EML4-ALK inversion results in a fusion protein with a constitutively active ALK kinase domain. Evidence of ALK rearrangement occurs in a minority (2-7%) of lung adenocarcinoma, and only ∼60% of these patients will respond to targeted ALK inhibition by drugs such as crizotinib and ceritinib. Clinically, targeted anti-ALK therapy is often initiated based on evidence of an ALK genomic rearrangement detected by fluorescence in situ hybridization (FISH) of interphase cells in formalin-fixed, paraffin-embedded tissue sections. At the genomic level, however, ALK rearrangements are heterogeneous, with multiple potential breakpoints in EML4, and alternate fusion partners. Using next-generation sequencing of DNA and RNA together with ALK immunohistochemistry, we comprehensively characterized genomic breakpoints in 33 FISH-positive lung adenocarcinomas. Of these 33 cases, 29 (88%) had detectable DNA level ALK rearrangements involving EML4, KIF5B, or non-canonical partners including ASXL2, ATP6V1B1, PRKAR1A, and SPDYA. A subset of 12 cases had material available for RNA-Seq. Of these, eight of eight (100%) cases with DNA rearrangements showed ALK fusion transcripts from RNA-Seq; three of four cases (75%) without detectable DNA rearrangements were similarly negative by RNA-Seq, and one case was positive by RNA-Seq but negative by DNA next-generation sequencing. By immunohistochemistry, 17 of 19 (89%) tested cases were clearly positive for ALK protein expression; the remaining cases had no detectable DNA level rearrangement or had a non-canonical rearrangement not predicted to form a fusion protein. Survival analysis of patients treated with targeted ALK inhibitors demonstrates a significant difference in mean survival between patients with next-generation sequencing confirmed EML4-ALK rearrangements, and those without (20.6 months vs 5.4 months, P<0.01). Together, these data demonstrate abundant genomic heterogeneity among ALK-rearranged lung adenocarcinoma, which may account for differences in treatment response with targeted ALK inhibitors.

Original languageEnglish
Pages (from-to)791-808
Number of pages18
JournalModern Pathology
Volume31
Issue number5
DOIs
StatePublished - May 1 2018

Fingerprint

Dive into the research topics of 'Genomic heterogeneity of ALK fusion breakpoints in non-small-cell lung cancer'. Together they form a unique fingerprint.

Cite this