Cargando…

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

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 cli...

Descripción completa

Detalles Bibliográficos
Autores principales: Rijavec, Erika, Coco, Simona, Genova, Carlo, Rossi, Giovanni, Longo, Luca, Grossi, Francesco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7017364/
https://www.ncbi.nlm.nih.gov/pubmed/31861557
http://dx.doi.org/10.3390/cancers12010017
_version_ 1783497182439014400
author Rijavec, Erika
Coco, Simona
Genova, Carlo
Rossi, Giovanni
Longo, Luca
Grossi, Francesco
author_facet Rijavec, Erika
Coco, Simona
Genova, Carlo
Rossi, Giovanni
Longo, Luca
Grossi, Francesco
author_sort Rijavec, Erika
collection PubMed
description 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.
format Online
Article
Text
id pubmed-7017364
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-70173642020-02-28 Liquid Biopsy in Non-Small Cell Lung Cancer: Highlights and Challenges Rijavec, Erika Coco, Simona Genova, Carlo Rossi, Giovanni Longo, Luca Grossi, Francesco Cancers (Basel) Review 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. MDPI 2019-12-19 /pmc/articles/PMC7017364/ /pubmed/31861557 http://dx.doi.org/10.3390/cancers12010017 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Rijavec, Erika
Coco, Simona
Genova, Carlo
Rossi, Giovanni
Longo, Luca
Grossi, Francesco
Liquid Biopsy in Non-Small Cell Lung Cancer: Highlights and Challenges
title Liquid Biopsy in Non-Small Cell Lung Cancer: Highlights and Challenges
title_full Liquid Biopsy in Non-Small Cell Lung Cancer: Highlights and Challenges
title_fullStr Liquid Biopsy in Non-Small Cell Lung Cancer: Highlights and Challenges
title_full_unstemmed Liquid Biopsy in Non-Small Cell Lung Cancer: Highlights and Challenges
title_short Liquid Biopsy in Non-Small Cell Lung Cancer: Highlights and Challenges
title_sort liquid biopsy in non-small cell lung cancer: highlights and challenges
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7017364/
https://www.ncbi.nlm.nih.gov/pubmed/31861557
http://dx.doi.org/10.3390/cancers12010017
work_keys_str_mv AT rijavecerika liquidbiopsyinnonsmallcelllungcancerhighlightsandchallenges
AT cocosimona liquidbiopsyinnonsmallcelllungcancerhighlightsandchallenges
AT genovacarlo liquidbiopsyinnonsmallcelllungcancerhighlightsandchallenges
AT rossigiovanni liquidbiopsyinnonsmallcelllungcancerhighlightsandchallenges
AT longoluca liquidbiopsyinnonsmallcelllungcancerhighlightsandchallenges
AT grossifrancesco liquidbiopsyinnonsmallcelllungcancerhighlightsandchallenges