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Erschienen in: Journal of Cancer Research and Clinical Oncology 5/2020

03.03.2020 | Original Article – Clinical Oncology

ALK detection in lung cancer: identification of atypical and cryptic ALK rearrangements using an optimal algorithm

verfasst von: Yuanyuan Liu, Shafei Wu, Xiaohua Shi, Zhiyong Liang, Xuan Zeng

Erschienen in: Journal of Cancer Research and Clinical Oncology | Ausgabe 5/2020

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Abstract

Purpose

IHC, FISH, and NGS are common methods of ALK evaluation in NSCLC. The purpose of this study was to investigate whether ALK false positives or false negatives occurred more often in daily routines. An approach to identify ALK fusion was then proposed.

Materials and methods

We analyzed 1815 cases of NSCLC, including 83 (4.6%) ALK IHC positives. Total 182 samples (62 ALK+ and 120 ALK−) were examined via FISH, RT-ddPCR, NGS, RT-qPCR and RNAscope to confirm ALK status.

Results

One ALK FISH false negative was found, which harbored two genomic rearrangements involved in EML4–ALK (exon 13:exon 20) fusion. One ALK IHC false negative was confirmed depending on a rare ALK FISH-positive pattern and ALK RNAscope positive but ALK fusion was not found via NGS. In addition, an atypical ALK FISH-positive pattern was observed in an IHC-positive case with chromosome 2 inversion leading to EML4–ALK (exon 6:exon 20) fusion. EML4–ALK fusion was determined in one case with an atypical FISH patterns by RT-qPCR. Rare complicated genomic rearrangements involved in a novel ALK fusion of EML4–ALK (exon 7:exon 14) were distinguished in an ALK IHC and FISH double-positive case.

Conclusion

False negative of ALK IHC, FISH and NGS results were found in our cohort, but none was false ALK positive. False ALK negatives should be more concerned than false positives. ALK rearrangements with cryptic ALK fusion patterns could be identified using our algorithm. Non-squamous non-small cell lung cancer was recommended for priority detection.
Literatur
Zurück zum Zitat Christopoulos P, Endris V, Bozorgmehr F et al (2018) EML4-ALK fusion variant V3 is a high-risk feature conferring accelerated metastatic spread, early treatment failure and worse overall survival in ALK+ non-small cell lung cancer. Int J Cancer 142:2589–2598. https://doi.org/10.1002/ijc.31275 CrossRefPubMed Christopoulos P, Endris V, Bozorgmehr F et al (2018) EML4-ALK fusion variant V3 is a high-risk feature conferring accelerated metastatic spread, early treatment failure and worse overall survival in ALK+ non-small cell lung cancer. Int J Cancer 142:2589–2598. https://​doi.​org/​10.​1002/​ijc.​31275 CrossRefPubMed
Zurück zum Zitat Lindeman NI, Cagle PT, Aisner DL et al (2018) Updated molecular testing guideline for the selection of lung cancer patients for treatment with targeted tyrosine kinase inhibitors: guideline from the College of American Pathologists, the International Association for the Study of Lung Cancer, and the Association for Molecular Pathology. J Thorac Oncol 13:323–358. https://doi.org/10.1016/j.jtho.2017.12.001 CrossRefPubMed Lindeman NI, Cagle PT, Aisner DL et al (2018) Updated molecular testing guideline for the selection of lung cancer patients for treatment with targeted tyrosine kinase inhibitors: guideline from the College of American Pathologists, the International Association for the Study of Lung Cancer, and the Association for Molecular Pathology. J Thorac Oncol 13:323–358. https://​doi.​org/​10.​1016/​j.​jtho.​2017.​12.​001 CrossRefPubMed
Zurück zum Zitat Soda M, Choi YL, Enomoto M et al (2007) Identification of the transforming EML4-ALK fusion gene in non-small-cell lung cancer. Nature 448:561–566CrossRef Soda M, Choi YL, Enomoto M et al (2007) Identification of the transforming EML4-ALK fusion gene in non-small-cell lung cancer. Nature 448:561–566CrossRef
Zurück zum Zitat Tuononen K, Mäki-Nevala S, Sarhadi VK et al (2013) Comparison of targeted next-generation sequencing (NGS) and real-time PCR in the detection of EGFR, KRAS, and BRAF mutations on formalin-fixed, paraffin-embedded tumor material of non-small cell lung carcinoma-superiority of NGS. Genes Chromosomes Cancer 52:503–511. https://doi.org/10.1002/gcc.22047 CrossRefPubMed Tuononen K, Mäki-Nevala S, Sarhadi VK et al (2013) Comparison of targeted next-generation sequencing (NGS) and real-time PCR in the detection of EGFR, KRAS, and BRAF mutations on formalin-fixed, paraffin-embedded tumor material of non-small cell lung carcinoma-superiority of NGS. Genes Chromosomes Cancer 52:503–511. https://​doi.​org/​10.​1002/​gcc.​22047 CrossRefPubMed
Metadaten
Titel
ALK detection in lung cancer: identification of atypical and cryptic ALK rearrangements using an optimal algorithm
verfasst von
Yuanyuan Liu
Shafei Wu
Xiaohua Shi
Zhiyong Liang
Xuan Zeng
Publikationsdatum
03.03.2020
Verlag
Springer Berlin Heidelberg
Erschienen in
Journal of Cancer Research and Clinical Oncology / Ausgabe 5/2020
Print ISSN: 0171-5216
Elektronische ISSN: 1432-1335
DOI
https://doi.org/10.1007/s00432-020-03166-1

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