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Liquid Biopsy in Non-Small Cell Lung Cancer: Highlights and Challenges.

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TLDR
In this regard, liquid biopsy represents a minimally invasive and more comprehensive option for early detection and investigation of this tumor.
Abstract
Non-small cell lung cancer is one leading cause of death worldwide, and patients would greatly benefit from an early diagnosis. Since targeted and immunotherapies have emerged as novel approaches for more tailored treatments, repeated assessments of the tumor biology have become pivotal to drive clinical decisions. Currently, tumor tissue biopsy is the gold standard to investigate potentially actionable biomarkers, but this procedure is invasive and may prove inadequate to represent the whole malignancy. In this regard, liquid biopsy represents a minimally invasive and more comprehensive option for early detection and investigation of this tumor. Today, cell-free DNA is the only approved circulating marker to select patients for a targeted therapy. Conversely, the other tumor-derived markers (i.e., circulating tumor cells, miRNAs, exosomes, and tumor educated platelets) are still at a pre-clinical phase, although they show promising results for their application in screening programs or as prognostic/predictive biomarkers. The main challenges for their clinical translation are the lack of reliable cutoffs and, especially for miRNAs, the great variability among the studies. Moreover, no established tool has been approved for circulating tumor cells and exosome isolation. Finally, large prospective clinical trials are mandatory to provide evidence of their clinical utility.

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Dealing with NSCLC EGFR mutation testing and treatment: A comprehensive review with an Italian real-world perspective.

TL;DR: A review of different detection platforms and therapeutic options currently available for the clinical management of advanced EGFR-positive NSCLC, summarizing scientific evidence and describing molecular testing as well as treatment practice in the real-word scenario is provided in this article.
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Clinical Impact of High Throughput Sequencing on Liquid Biopsy in Advanced Solid Cancer

TL;DR: Routine cfDNA molecular profiling is feasible and can lead to the access of targeted therapies, however, no notable benefit in patient’s outcomes was shown in this unselected pan-cancer study.
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Liquid Biopsy for Cancer Cachexia: Focus on Muscle-Derived microRNAs

TL;DR: The current knowledge on circulating muscular miRNAs involved in muscle atrophy is summarized, since they might represent easily accessible and promising biomarkers of cachexia and might allow an early diagnosis of this syndrome.
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High-Sensitive Detection of Small-Cell Lung Cancer Cells Based on Terminal Deoxynucleotidyl Transferase-Mediated Extension Polymerization Aptamer Probe.

TL;DR: In this article, a terminal deoxynucleotidyl transferase (TdT)-mediated extension polymerization aptamer probe (denoted as TEPAP) was designed for the detection of small-cell lung cancer (SCLC).
References
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Journal ArticleDOI

The functions of animal microRNAs

TL;DR: Evidence is mounting that animal miRNAs are more numerous, and their regulatory impact more pervasive, than was previously suspected.
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Isolation of rare circulating tumour cells in cancer patients by microchip technology.

TL;DR: The CTC-chip successfully identified CTCs in the peripheral blood of patients with metastatic lung, prostate, pancreatic, breast and colon cancer in 115 of 116 samples, with a range of 5–1,281CTCs per ml and approximately 50% purity.
Journal ArticleDOI

Argonaute2 complexes carry a population of circulating microRNAs independent of vesicles in human plasma

TL;DR: Identification of extracellular Ago2–miRNA complexes in plasma raises the possibility that cells release a functional miRNA-induced silencing complex into the circulation, and reveals two populations of circulating miRNAs and suggest that circulating Ago2 complexes are a mechanism responsible for the stability of plasma mi RNAs.
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What are the challenges in non-small cell lung cancer diagnosis?

The challenges in non-small cell lung cancer diagnosis include the lack of reliable cutoffs for circulating tumor markers and the need for large prospective clinical trials.