Suscribirse

Liquid biopsy as a tool for KRAS/NRAS/BRAF baseline testing in metastatic colorectal cancer - 13/07/24

Doi : 10.1016/j.clinre.2024.102417 
Hampig Raphael Kourie 1, , Joseph Zouein 1, 2, Ziad Zalaquett 1, Alain Chebly 3, 4, Lewis Nasr 1, Fadi El Karak 1, Maroun Sadek 5, Ousama Safar 6, Mouin Fouani 7, Nizar Bitar 8, Kamal Kachmar 9, Fady Nasr 1, Fadi Farhat 10, Jawad Makarem 11, Joseph Kattan 1, Julien Taieb 12
1 Hematology-Oncology Department, Hôtel-Dieu de France University Hospital, Saint Joseph University, Beirut, Lebanon 
2 Department of Medicine, Duke University Medical Center, Durham, NC, USA 
3 Jacques Loiselet Center for Medical Genetics and Genomics (CGGM), Faculty of Medicine, Saint Joseph University, Beirut, Lebanon 
4 Higher Institute of Public Health, Saint Joseph University, Beirut, Lebanon 
5 Hematology-Oncology Department, Lebanese Hospital Geitaoui, Beirut, Lebanon 
6 Dar Al Amal University Hospital, Bekaa, Lebanon 
7 Saint George Hospital, Hadath, Lebanon 
8 Sahel General Hospital, Beirut, Lebanon 
9 Tebnin Governmental Hospital, Bekaa, Lebanon 
10 Mount Lebanon Hospital, Baabda, Lebanon 
11 Al Jabal Hospital, Chouf, Lebanon 
12 Hôpital Européen Georges Pompidou, Paris, France 

Corresponding author. Hampig Raphael Kourie. Hematology Oncology Department, Hotel Dieu de France, boulevard Alfred Naccache, Beirut, Lebanon. Tel.: +961 1 604 000 Ext:9716Hematology Oncology Department, Hotel Dieu de France, boulevard Alfred NaccacheBeirutLebanon
En prensa. Manuscrito Aceptado. Disponible en línea desde el Saturday 13 July 2024
This article has been published in an issue click here to access

Highlights

Liquid biopsy using Idylla RT-PCR has a sensitivity of 62% and a specificity of 93% compared with tissue biopsy for detecting KRAS/NRAS/BRAF mutations in metastatic colorectal cancer.
The most frequent mutations detected by liquid and tissue biopsy are KRAS (41%), followed by NRAS (4%) and BRAF (3%).
No relationship was established between the presence of hepatic metastasis, peritoneal carcinomatosis, pulmonary metastasis or tumor localization and RAS status concordance between liquid and tissue biopsy.

El texto completo de este artículo está disponible en PDF.

Abstract

Background

The absence of KRAS and NRAS gene mutations (RAS wild type) in metastatic colorectal cancer (mCRC), is associated with a good response to targeted therapy with anti-EGFR receptor antibodies. The current gold standard for RAS mutational status identification is genetic testing on tissue biopsy samples.

Objective

This study aimed to assess the relevance of liquid biopsy as a less invasive alternative to tissue biopsy for detecting KRAS/NRAS and BRAF mutations in patients with metastatic colorectal cancer (mCRC). The study also aimed to determine the concordance between liquid biopsy and tissue biopsy.

Methods

This is a phase IV, observational, uncontrolled, non-comparative, non-randomized, open label study. RAS/BRAF status will be tested at baseline using tissue and liquid biopsy using the Idylla/Biocartis PCR-based device. The primary endpoint is the comparison of the RAS status based on liquid biopsy with the RAS status based on tissue biopsy.

Results

100 patients with mCRC were included in the study. 75% of patients showed concordant results between liquid biopsy and tissue biopsy, while 25% had discordant results. Liquid biopsy demonstrated a sensitivity of 62% and a specificity of 93%. The accuracy of liquid biopsy was 75%, with a moderate agreement between the two tests. The most frequent mutations in concordant cases were in KRAS (41%), followed by NRAS (4%) and BRAF (3%). Mutations were not detected in 42% of tissue biopsy samples and 60% of liquid biopsy samples. The presence of hepatic metastases did not significantly affect the concordance between the biopsy methods.

Conclusion

Liquid biopsy using the Idylla™ system showed a relatively low sensitivity but high specificity for detecting KRAS/NRAS and BRAF mutations in mCRC patients. Despite some discordant cases, liquid biopsy remains a promising alternative to tissue biopsy due to its non-invasiveness, ability to provide multiple samples, and better representation of tumor heterogeneity.

El texto completo de este artículo está disponible en PDF.

Keywords : Keyword


Esquema


© 2024  Publicado por Elsevier Masson SAS.
Añadir a mi biblioteca Eliminar de mi biblioteca Imprimir
Exportación

    Exportación citas

  • Fichero

  • Contenido

Bienvenido a EM-consulte, la referencia de los profesionales de la salud.
El acceso al texto completo de este artículo requiere una suscripción.

¿Ya suscrito a @@106933@@ revista ?

Mi cuenta


Declaración CNIL

EM-CONSULTE.COM se declara a la CNIL, la declaración N º 1286925.

En virtud de la Ley N º 78-17 del 6 de enero de 1978, relativa a las computadoras, archivos y libertades, usted tiene el derecho de oposición (art.26 de la ley), el acceso (art.34 a 38 Ley), y correcta (artículo 36 de la ley) los datos que le conciernen. Por lo tanto, usted puede pedir que se corrija, complementado, clarificado, actualizado o suprimido información sobre usted que son inexactos, incompletos, engañosos, obsoletos o cuya recogida o de conservación o uso está prohibido.
La información personal sobre los visitantes de nuestro sitio, incluyendo su identidad, son confidenciales.
El jefe del sitio en el honor se compromete a respetar la confidencialidad de los requisitos legales aplicables en Francia y no de revelar dicha información a terceros.


Todo el contenido en este sitio: Copyright © 2024 Elsevier, sus licenciantes y colaboradores. Se reservan todos los derechos, incluidos los de minería de texto y datos, entrenamiento de IA y tecnologías similares. Para todo el contenido de acceso abierto, se aplican los términos de licencia de Creative Commons.