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Evaluation of RAS Mutational Status in Liquid Biopsy to Monitor Disease Progression in Metastatic Colorectal Cancer Patients
In this study we evaluated both~ K- and N-RAS mutations in plasma samples from patients with metastatic colorectal cancer by means of the BEAMing technology, and we assessed their diagnostic performance compared to RAS analyses performed on tissue. The sensitivity of BEAMing in identifying KRAS muta...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10253213/ https://www.ncbi.nlm.nih.gov/pubmed/37296579 http://dx.doi.org/10.3390/cells12111458 |
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author | Lastraioli, Elena Bettiol, Alessandra Iorio, Jessica Limatola, Elvira Checcacci, Daniele Parisi, Erica Bianchi, Cristina Arcangeli, Annarosa Iannopollo, Mauro Di Costanzo, Francesco Di Lieto, Marco |
author_facet | Lastraioli, Elena Bettiol, Alessandra Iorio, Jessica Limatola, Elvira Checcacci, Daniele Parisi, Erica Bianchi, Cristina Arcangeli, Annarosa Iannopollo, Mauro Di Costanzo, Francesco Di Lieto, Marco |
author_sort | Lastraioli, Elena |
collection | PubMed |
description | In this study we evaluated both~ K- and N-RAS mutations in plasma samples from patients with metastatic colorectal cancer by means of the BEAMing technology, and we assessed their diagnostic performance compared to RAS analyses performed on tissue. The sensitivity of BEAMing in identifying KRAS mutations was of 89.5%, with a fair specificity. The agreement with tissue analysis was moderate. The sensitivity for NRAS was high with a good specificity, and the agreement between tissue analysis and BEAMing was fair. Interestingly, significantly higher mutant allele fraction (MAF) levels were detected in patients with G2 tumors, liver metastases, and in those who did not receive surgery. NRAS MAF level was significantly higher in patients with mucinous adenocarcinoma and for those with lung metastases. A sharp increase in the MAF values was observed in patients who moved towards disease progression. More strikingly, molecular progression always anticipated the radiological one in these patients. These observations pave the way to the possibility of using liquid biopsy to monitor patients during treatment, and to enable oncologists to anticipate interventions compared to radiological analyses. This will allow time to be saved and ensure a better management of metastatic patients in the near future. |
format | Online Article Text |
id | pubmed-10253213 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-102532132023-06-10 Evaluation of RAS Mutational Status in Liquid Biopsy to Monitor Disease Progression in Metastatic Colorectal Cancer Patients Lastraioli, Elena Bettiol, Alessandra Iorio, Jessica Limatola, Elvira Checcacci, Daniele Parisi, Erica Bianchi, Cristina Arcangeli, Annarosa Iannopollo, Mauro Di Costanzo, Francesco Di Lieto, Marco Cells Article In this study we evaluated both~ K- and N-RAS mutations in plasma samples from patients with metastatic colorectal cancer by means of the BEAMing technology, and we assessed their diagnostic performance compared to RAS analyses performed on tissue. The sensitivity of BEAMing in identifying KRAS mutations was of 89.5%, with a fair specificity. The agreement with tissue analysis was moderate. The sensitivity for NRAS was high with a good specificity, and the agreement between tissue analysis and BEAMing was fair. Interestingly, significantly higher mutant allele fraction (MAF) levels were detected in patients with G2 tumors, liver metastases, and in those who did not receive surgery. NRAS MAF level was significantly higher in patients with mucinous adenocarcinoma and for those with lung metastases. A sharp increase in the MAF values was observed in patients who moved towards disease progression. More strikingly, molecular progression always anticipated the radiological one in these patients. These observations pave the way to the possibility of using liquid biopsy to monitor patients during treatment, and to enable oncologists to anticipate interventions compared to radiological analyses. This will allow time to be saved and ensure a better management of metastatic patients in the near future. MDPI 2023-05-24 /pmc/articles/PMC10253213/ /pubmed/37296579 http://dx.doi.org/10.3390/cells12111458 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Lastraioli, Elena Bettiol, Alessandra Iorio, Jessica Limatola, Elvira Checcacci, Daniele Parisi, Erica Bianchi, Cristina Arcangeli, Annarosa Iannopollo, Mauro Di Costanzo, Francesco Di Lieto, Marco Evaluation of RAS Mutational Status in Liquid Biopsy to Monitor Disease Progression in Metastatic Colorectal Cancer Patients |
title | Evaluation of RAS Mutational Status in Liquid Biopsy to Monitor Disease Progression in Metastatic Colorectal Cancer Patients |
title_full | Evaluation of RAS Mutational Status in Liquid Biopsy to Monitor Disease Progression in Metastatic Colorectal Cancer Patients |
title_fullStr | Evaluation of RAS Mutational Status in Liquid Biopsy to Monitor Disease Progression in Metastatic Colorectal Cancer Patients |
title_full_unstemmed | Evaluation of RAS Mutational Status in Liquid Biopsy to Monitor Disease Progression in Metastatic Colorectal Cancer Patients |
title_short | Evaluation of RAS Mutational Status in Liquid Biopsy to Monitor Disease Progression in Metastatic Colorectal Cancer Patients |
title_sort | evaluation of ras mutational status in liquid biopsy to monitor disease progression in metastatic colorectal cancer patients |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10253213/ https://www.ncbi.nlm.nih.gov/pubmed/37296579 http://dx.doi.org/10.3390/cells12111458 |
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