[HTML][HTML] Next generation sequencing for gene fusion analysis in lung cancer: a literature review

R Bruno, G Fontanini - Diagnostics, 2020 - mdpi.com
Gene fusions have a pivotal role in non-small cell lung cancer (NSCLC) precision medicine.
Several techniques can be used, from fluorescence in situ hybridization and …

Rediscovering immunohistochemistry in lung cancer

A La Salvia, ML Meyer, FR Hirsch, KM Kerr… - Critical Reviews in …, 2024 - Elsevier
Several observations indicate that protein expression analysis by immunohistochemistry
(IHC) remains relevant in individuals with non-small-cell lung cancer (NSCLC) when …

[HTML][HTML] Blood first assay screening trial (BFAST) in treatment-naive advanced or metastatic NSCLC: initial results of the phase 2 ALK-positive cohort

R Dziadziuszko, T Mok, S Peters, JY Han… - Journal of Thoracic …, 2021 - Elsevier
Abstract Introduction The Blood First Assay Screening Trial is an ongoing open-label,
multicohort study, prospectively evaluating the relationship between blood-based next …

[HTML][HTML] Mutation-tailored treatment selection in non-small cell lung cancer patients in daily clinical practice

EMP Steeghs, HJM Groen, E Schuuring, MJ Aarts… - Lung Cancer, 2022 - Elsevier
Objectives The number of targeted drugs in non-small cell lung cancer (NSCLC) is ever-
expanding and requires testing of an increasing number of predictive biomarkers. We …

[HTML][HTML] Fluorescence in Situ Hybridization (FISH) for Detecting Anaplastic Lymphoma Kinase (ALK) Rearrangement in Lung Cancer: Clinically Relevant Technical …

Z Tang, L Wang, G Tang, LJ Medeiros - International journal of molecular …, 2019 - mdpi.com
In 2011, the Vysis Break Apart ALK fluorescence in situ hybridization (FISH) assay was
approved by the United States Food and Drug Administration as a companion diagnostic for …

Sequencing strategies for fusion gene detection

EE Heyer, J Blackburn - Bioessays, 2020 - Wiley Online Library
Fusion genes formed by chromosomal rearrangements are common drivers of cancer.
Recent innovations in the field of next‐generation sequencing (NGS) have seen a dynamic …

Fusion transcript discovery using RNA sequencing in formalin-fixed paraffin-embedded specimen

A Talebi, JP Thiery, MA Kerachian - Critical Reviews in Oncology …, 2021 - Elsevier
Chimeric transcripts are critical for diagnosis or prognosis and could constitute effective
therapeutic targets. Fresh tissues are the major source for the identification of these fusion …

Comprehensive NGS profiling to enable detection of ALK gene rearrangements and MET amplifications in non-small cell lung cancer

S Clavé, JB Jackson, M Salido, J Kames… - Frontiers in …, 2023 - frontiersin.org
Introduction Next-generation sequencing (NGS) is currently widely used for biomarker
studies and molecular profiling to identify concurrent alterations that can lead to the better …

Detection of clinically actionable gene fusions by next‐generation sequencing‐based RNA sequencing of non–small cell lung cancer cytology specimens: A single …

J Diks, Z Tang, M Altan, S Anderson… - Cancer …, 2024 - Wiley Online Library
Background Genomic profiling is needed to identify actionable alterations in non–small cell
lung cancer (NSCLC). Panel‐based testing such as next‐generation sequencing (NGS) is …

[HTML][HTML] The Transition from Cancer “omics” to “epi-omics” through Next-and Third-Generation Sequencing

K Athanasopoulou, GN Daneva, MA Boti, G Dimitroulis… - Life, 2022 - mdpi.com
Deciphering cancer etiopathogenesis has proven to be an especially challenging task since
the mechanisms that drive tumor development and progression are far from simple. An …