Cargando…

Plasma ctDNA RAS mutation analysis for the diagnosis and treatment monitoring of metastatic colorectal cancer patients

BACKGROUND: RAS assessment is mandatory for therapy decision in metastatic colorectal cancer (mCRC) patients. This determination is based on tumor tissue, however, genotyping of circulating tumor (ct)DNA offers clear advantages as a minimally invasive method that represents tumor heterogeneity. Our...

Descripción completa

Detalles Bibliográficos
Autores principales: Vidal, J, Muinelo, L, Dalmases, A, Jones, F, Edelstein, D, Iglesias, M, Orrillo, M, Abalo, A, Rodríguez, C, Brozos, E, Vidal, Y, Candamio, S, Vázquez, F, Ruiz, J, Guix, M, Visa, L, Sikri, V, Albanell, J, Bellosillo, B, López, R, Montagut, C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5834035/
https://www.ncbi.nlm.nih.gov/pubmed/28419195
http://dx.doi.org/10.1093/annonc/mdx125
_version_ 1783303583659196416
author Vidal, J
Muinelo, L
Dalmases, A
Jones, F
Edelstein, D
Iglesias, M
Orrillo, M
Abalo, A
Rodríguez, C
Brozos, E
Vidal, Y
Candamio, S
Vázquez, F
Ruiz, J
Guix, M
Visa, L
Sikri, V
Albanell, J
Bellosillo, B
López, R
Montagut, C
author_facet Vidal, J
Muinelo, L
Dalmases, A
Jones, F
Edelstein, D
Iglesias, M
Orrillo, M
Abalo, A
Rodríguez, C
Brozos, E
Vidal, Y
Candamio, S
Vázquez, F
Ruiz, J
Guix, M
Visa, L
Sikri, V
Albanell, J
Bellosillo, B
López, R
Montagut, C
author_sort Vidal, J
collection PubMed
description BACKGROUND: RAS assessment is mandatory for therapy decision in metastatic colorectal cancer (mCRC) patients. This determination is based on tumor tissue, however, genotyping of circulating tumor (ct)DNA offers clear advantages as a minimally invasive method that represents tumor heterogeneity. Our study aims to evaluate the use of ctDNA as an alternative for determining baseline RAS status and subsequent monitoring of RAS mutations during therapy as a component of routine clinical practice. PATIENTS AND METHODS: RAS mutational status in plasma was evaluated in mCRC patients by OncoBEAM™ RAS CRC assay. Concordance of results in plasma and tissue was retrospectively evaluated. RAS mutations were also prospectively monitored in longitudinal plasma samples from selected patients. RESULTS: Analysis of RAS in tissue and plasma samples from 115 mCRC patients showed a 93% overall agreement. Plasma/tissue RAS discrepancies were mainly explained by spatial and temporal tumor heterogeneity. Analysis of clinico-pathological features showed that the site of metastasis (i.e. peritoneal, lung), the histology of the tumor (i.e. mucinous) and administration of treatment previous to blood collection negatively impacted the detection of RAS in ctDNA. In patients with baseline mutant RAS tumors treated with chemotherapy/antiangiogenic, longitudinal analysis of RAS ctDNA mirrored response to treatment, being an early predictor of response. In patients RAS wt, longitudinal monitoring of RAS ctDNA revealed that OncoBEAM was useful to detect emergence of RAS mutations during anti-EGFR treatment. CONCLUSION: The high overall agreement in RAS mutational assessment between plasma and tissue supports blood-based testing with OncoBEAM™ as a viable alternative for genotyping RAS of mCRC patients in routine clinical practice. Our study describes practical clinico-pathological specifications to optimize RAS ctDNA determination. Moreover, OncoBEAM™ is useful to monitor RAS in patients undergoing systemic therapy to detect resistance and evaluate the efficacy of particular treatments.
format Online
Article
Text
id pubmed-5834035
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-58340352018-03-07 Plasma ctDNA RAS mutation analysis for the diagnosis and treatment monitoring of metastatic colorectal cancer patients Vidal, J Muinelo, L Dalmases, A Jones, F Edelstein, D Iglesias, M Orrillo, M Abalo, A Rodríguez, C Brozos, E Vidal, Y Candamio, S Vázquez, F Ruiz, J Guix, M Visa, L Sikri, V Albanell, J Bellosillo, B López, R Montagut, C Ann Oncol Original Articles BACKGROUND: RAS assessment is mandatory for therapy decision in metastatic colorectal cancer (mCRC) patients. This determination is based on tumor tissue, however, genotyping of circulating tumor (ct)DNA offers clear advantages as a minimally invasive method that represents tumor heterogeneity. Our study aims to evaluate the use of ctDNA as an alternative for determining baseline RAS status and subsequent monitoring of RAS mutations during therapy as a component of routine clinical practice. PATIENTS AND METHODS: RAS mutational status in plasma was evaluated in mCRC patients by OncoBEAM™ RAS CRC assay. Concordance of results in plasma and tissue was retrospectively evaluated. RAS mutations were also prospectively monitored in longitudinal plasma samples from selected patients. RESULTS: Analysis of RAS in tissue and plasma samples from 115 mCRC patients showed a 93% overall agreement. Plasma/tissue RAS discrepancies were mainly explained by spatial and temporal tumor heterogeneity. Analysis of clinico-pathological features showed that the site of metastasis (i.e. peritoneal, lung), the histology of the tumor (i.e. mucinous) and administration of treatment previous to blood collection negatively impacted the detection of RAS in ctDNA. In patients with baseline mutant RAS tumors treated with chemotherapy/antiangiogenic, longitudinal analysis of RAS ctDNA mirrored response to treatment, being an early predictor of response. In patients RAS wt, longitudinal monitoring of RAS ctDNA revealed that OncoBEAM was useful to detect emergence of RAS mutations during anti-EGFR treatment. CONCLUSION: The high overall agreement in RAS mutational assessment between plasma and tissue supports blood-based testing with OncoBEAM™ as a viable alternative for genotyping RAS of mCRC patients in routine clinical practice. Our study describes practical clinico-pathological specifications to optimize RAS ctDNA determination. Moreover, OncoBEAM™ is useful to monitor RAS in patients undergoing systemic therapy to detect resistance and evaluate the efficacy of particular treatments. Oxford University Press 2017-06 2017-04-13 /pmc/articles/PMC5834035/ /pubmed/28419195 http://dx.doi.org/10.1093/annonc/mdx125 Text en © The Author 2017. Published by Oxford University Press on behalf of the European Society for Medical Oncology. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Vidal, J
Muinelo, L
Dalmases, A
Jones, F
Edelstein, D
Iglesias, M
Orrillo, M
Abalo, A
Rodríguez, C
Brozos, E
Vidal, Y
Candamio, S
Vázquez, F
Ruiz, J
Guix, M
Visa, L
Sikri, V
Albanell, J
Bellosillo, B
López, R
Montagut, C
Plasma ctDNA RAS mutation analysis for the diagnosis and treatment monitoring of metastatic colorectal cancer patients
title Plasma ctDNA RAS mutation analysis for the diagnosis and treatment monitoring of metastatic colorectal cancer patients
title_full Plasma ctDNA RAS mutation analysis for the diagnosis and treatment monitoring of metastatic colorectal cancer patients
title_fullStr Plasma ctDNA RAS mutation analysis for the diagnosis and treatment monitoring of metastatic colorectal cancer patients
title_full_unstemmed Plasma ctDNA RAS mutation analysis for the diagnosis and treatment monitoring of metastatic colorectal cancer patients
title_short Plasma ctDNA RAS mutation analysis for the diagnosis and treatment monitoring of metastatic colorectal cancer patients
title_sort plasma ctdna ras mutation analysis for the diagnosis and treatment monitoring of metastatic colorectal cancer patients
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5834035/
https://www.ncbi.nlm.nih.gov/pubmed/28419195
http://dx.doi.org/10.1093/annonc/mdx125
work_keys_str_mv AT vidalj plasmactdnarasmutationanalysisforthediagnosisandtreatmentmonitoringofmetastaticcolorectalcancerpatients
AT muinelol plasmactdnarasmutationanalysisforthediagnosisandtreatmentmonitoringofmetastaticcolorectalcancerpatients
AT dalmasesa plasmactdnarasmutationanalysisforthediagnosisandtreatmentmonitoringofmetastaticcolorectalcancerpatients
AT jonesf plasmactdnarasmutationanalysisforthediagnosisandtreatmentmonitoringofmetastaticcolorectalcancerpatients
AT edelsteind plasmactdnarasmutationanalysisforthediagnosisandtreatmentmonitoringofmetastaticcolorectalcancerpatients
AT iglesiasm plasmactdnarasmutationanalysisforthediagnosisandtreatmentmonitoringofmetastaticcolorectalcancerpatients
AT orrillom plasmactdnarasmutationanalysisforthediagnosisandtreatmentmonitoringofmetastaticcolorectalcancerpatients
AT abaloa plasmactdnarasmutationanalysisforthediagnosisandtreatmentmonitoringofmetastaticcolorectalcancerpatients
AT rodriguezc plasmactdnarasmutationanalysisforthediagnosisandtreatmentmonitoringofmetastaticcolorectalcancerpatients
AT brozose plasmactdnarasmutationanalysisforthediagnosisandtreatmentmonitoringofmetastaticcolorectalcancerpatients
AT vidaly plasmactdnarasmutationanalysisforthediagnosisandtreatmentmonitoringofmetastaticcolorectalcancerpatients
AT candamios plasmactdnarasmutationanalysisforthediagnosisandtreatmentmonitoringofmetastaticcolorectalcancerpatients
AT vazquezf plasmactdnarasmutationanalysisforthediagnosisandtreatmentmonitoringofmetastaticcolorectalcancerpatients
AT ruizj plasmactdnarasmutationanalysisforthediagnosisandtreatmentmonitoringofmetastaticcolorectalcancerpatients
AT guixm plasmactdnarasmutationanalysisforthediagnosisandtreatmentmonitoringofmetastaticcolorectalcancerpatients
AT visal plasmactdnarasmutationanalysisforthediagnosisandtreatmentmonitoringofmetastaticcolorectalcancerpatients
AT sikriv plasmactdnarasmutationanalysisforthediagnosisandtreatmentmonitoringofmetastaticcolorectalcancerpatients
AT albanellj plasmactdnarasmutationanalysisforthediagnosisandtreatmentmonitoringofmetastaticcolorectalcancerpatients
AT bellosillob plasmactdnarasmutationanalysisforthediagnosisandtreatmentmonitoringofmetastaticcolorectalcancerpatients
AT lopezr plasmactdnarasmutationanalysisforthediagnosisandtreatmentmonitoringofmetastaticcolorectalcancerpatients
AT montagutc plasmactdnarasmutationanalysisforthediagnosisandtreatmentmonitoringofmetastaticcolorectalcancerpatients