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Monitoring of RAS mutant clones in plasma of patients with RAS mutant metastatic colorectal cancer

PURPOSE: Some patients with histologically confirmed primary mCRC and mutated RAS reported undetectable RAS mutant clones in plasma after receiving anti-VEGF treatment. The aim was to prospectively assess it with its potential therapeutic implications. METHODS: RAS mutant genes in solid biopsy (befo...

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Autores principales: Fernández Montes, A., Élez, E., Vivancos, A., Martínez, N., González, P., Covela, M., de la Cámara, J., Cousillas, A., Méndez, J. C., Graña, B., Aranda, E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9107427/
https://www.ncbi.nlm.nih.gov/pubmed/34997474
http://dx.doi.org/10.1007/s12094-021-02767-7
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author Fernández Montes, A.
Élez, E.
Vivancos, A.
Martínez, N.
González, P.
Covela, M.
de la Cámara, J.
Cousillas, A.
Méndez, J. C.
Graña, B.
Aranda, E.
author_facet Fernández Montes, A.
Élez, E.
Vivancos, A.
Martínez, N.
González, P.
Covela, M.
de la Cámara, J.
Cousillas, A.
Méndez, J. C.
Graña, B.
Aranda, E.
author_sort Fernández Montes, A.
collection PubMed
description PURPOSE: Some patients with histologically confirmed primary mCRC and mutated RAS reported undetectable RAS mutant clones in plasma after receiving anti-VEGF treatment. The aim was to prospectively assess it with its potential therapeutic implications. METHODS: RAS mutant genes in solid biopsy (before first-line treatment: FOLFOX/CAPOX + bevacizumab) were compared in liquid biopsy (before second-line treatment: panitumumab + FOLFIRI), using Idylla™ system. Discordant results between solid/liquid biopsies were assessed by the next-generation sequencing (NGS) test (solid/liquid biopsies). RESULTS: Twenty-three patients were assessed (seven had RAS mutant discrepancies between solid/liquid biopsies). The NGS test confirmed that 3/23 (13%) patients had undetectable RAS mutant clones in liquid biopsy and 3/23 (13%) presented discrepancies in solid biopsy (Idylla™ system vs. NGS test). CONCLUSION: Thirteen percentage of patients had undetectable RAS mutant clones in liquid biopsy after first-line treatment. However, some discrepancies between solid and liquid biopsies have been observed. These results suggest a need to improve accuracy of RAS analyses, especially in solid biopsies.
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spelling pubmed-91074272022-05-16 Monitoring of RAS mutant clones in plasma of patients with RAS mutant metastatic colorectal cancer Fernández Montes, A. Élez, E. Vivancos, A. Martínez, N. González, P. Covela, M. de la Cámara, J. Cousillas, A. Méndez, J. C. Graña, B. Aranda, E. Clin Transl Oncol Brief Research Article PURPOSE: Some patients with histologically confirmed primary mCRC and mutated RAS reported undetectable RAS mutant clones in plasma after receiving anti-VEGF treatment. The aim was to prospectively assess it with its potential therapeutic implications. METHODS: RAS mutant genes in solid biopsy (before first-line treatment: FOLFOX/CAPOX + bevacizumab) were compared in liquid biopsy (before second-line treatment: panitumumab + FOLFIRI), using Idylla™ system. Discordant results between solid/liquid biopsies were assessed by the next-generation sequencing (NGS) test (solid/liquid biopsies). RESULTS: Twenty-three patients were assessed (seven had RAS mutant discrepancies between solid/liquid biopsies). The NGS test confirmed that 3/23 (13%) patients had undetectable RAS mutant clones in liquid biopsy and 3/23 (13%) presented discrepancies in solid biopsy (Idylla™ system vs. NGS test). CONCLUSION: Thirteen percentage of patients had undetectable RAS mutant clones in liquid biopsy after first-line treatment. However, some discrepancies between solid and liquid biopsies have been observed. These results suggest a need to improve accuracy of RAS analyses, especially in solid biopsies. Springer International Publishing 2022-01-07 2022 /pmc/articles/PMC9107427/ /pubmed/34997474 http://dx.doi.org/10.1007/s12094-021-02767-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Brief Research Article
Fernández Montes, A.
Élez, E.
Vivancos, A.
Martínez, N.
González, P.
Covela, M.
de la Cámara, J.
Cousillas, A.
Méndez, J. C.
Graña, B.
Aranda, E.
Monitoring of RAS mutant clones in plasma of patients with RAS mutant metastatic colorectal cancer
title Monitoring of RAS mutant clones in plasma of patients with RAS mutant metastatic colorectal cancer
title_full Monitoring of RAS mutant clones in plasma of patients with RAS mutant metastatic colorectal cancer
title_fullStr Monitoring of RAS mutant clones in plasma of patients with RAS mutant metastatic colorectal cancer
title_full_unstemmed Monitoring of RAS mutant clones in plasma of patients with RAS mutant metastatic colorectal cancer
title_short Monitoring of RAS mutant clones in plasma of patients with RAS mutant metastatic colorectal cancer
title_sort monitoring of ras mutant clones in plasma of patients with ras mutant metastatic colorectal cancer
topic Brief Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9107427/
https://www.ncbi.nlm.nih.gov/pubmed/34997474
http://dx.doi.org/10.1007/s12094-021-02767-7
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