Abstract

Patients with advanced stage non-small cell lung carcinoma (NSCLC) harboring an anaplastic lymphoma kinase ALK gene rearrangement, detected from a tissue sample, can benefit from targeted ALK inhibitor treatment. However, while treatment is initially effective in most cases, relapse or progression occurs due to different resistance mechanisms including mutations in the tyrosine kinase domain of echinoderm microtubule-associated protein-like 4 (EML44)-ALK. The liquid biopsy concept has recently radically changed the clinical care of NSCLC patients, in particular for those harboring an epidermal growth factor receptor (EGFR) gene mutation. Therefore, liquid biopsy is an alternative or complementary method to tissue biopsy for the detection of some resistance mutations in EGFR arising during tyrosine kinase inhibitor treatment. Moreover, in some frail patients, or if the tumor lesion is not accessible to a tissue biopsy, a liquid biopsy can also detect some activating mutations in EGFR on initial assessment. Recent studies have evaluated the possibility of also using a liquid biopsy approach to detect an ALK rearrangement and/or the emergence during inhibitor treatment of some resistance mutations in ALK. These assessments can be performed by studying circulating tumor cells by fluorescent in situ hybridization and by immunocytochemistry and/or after the isolation of RNA from plasma samples, free or associated with platelets. Thus, the liquid biopsy may be a complementary or sometimes alternative method for the assessment of the ALK status in certain NSCLC patients, as well as a non-invasive approach for early detection of ALK mutations. In this review, we highlight the current data concerning the role of the liquid biopsy for the ALK status assessment for NSCLC patients, and we compare the different approaches for this evaluation from blood samples.

Highlights

  • Echinoderm microtubule-associated protein-like 4- anaplastic lymphoma kinase EML4-ALK gene rearrangements are present in around 5% of non-small cell lung carcinoma (NSCLC) patients [1,2]

  • It is important to note that depending on the treatment used to target an ALK rearrangement, the resistance mutations that emerge on the ALK gene can be different [15]

  • ALK rearrangements and ALK mutations can be detected with a liquid biopsies (LB)

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Summary

Introduction

Echinoderm microtubule-associated protein-like 4- anaplastic lymphoma kinase EML4-ALK gene rearrangements are present in around 5% of non-small cell lung carcinoma (NSCLC) patients [1,2]. Analysis for the EML4-ALK status is mainly performed by immunohistochemistry (IHC) and confirmed by FISH analysis from tissue biopsies [3,4] This status can be detected on cytological samples by immunochemistry (ICC) and/or by FISH analysis [5,6,7,8,9]. Cancers 2017, 9, 106 a change in targeted therapy [13,14] In most cases, this tumor progression is linked to the emergence of EML4-ALK mutations [15]. This review will briefly discuss the notion of LB and analyze the advantages and limitations of the different methods that evaluate the ALK status using blood from patients with advanced stage lung cancer, performed either at the time of diagnosis or during follow-up of the patient on targeted treatments

The Different Biological Components of a Liquid Biopsy
Analysis of the ALK Status with Circulating Tumor Cells
Analysis of ALK Status with Plasma
Analysis of the Status of ALK in Platelets
Detection of ALK Mutations in Liquid Biopsies
Advantages and Limits of the Liquid Biopsies for the Assessment of ALK Status
Centrifugation procedure
Conclusions

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