Liquid biopsy in oncology: a consensus statement of the Spanish Society of Pathology and the Spanish Society of Medical Oncology

Remon, J. ; García-Campelo, R. ; de Alava, E. ; Vera, R. ; Rodriguez-Peralto, J.L. ; Rodriguez-Lescure, A. ; Bellosillo, B. ; Garrido, P. ; Rojo, F. ; Alvarez-Alegret, R. (Universidad de Zaragoza)

Resumen: The proportion of cancer patients with tumours that harbour a potentially targetable genomic alteration is growing considerably. The diagnosis of these genomic alterations can lead to tailored treatment at the onset of disease or on progression and to obtaining additional predictive information on immunotherapy efficacy. However, in up to 25% of cases, the initial tissue biopsy is inadequate for precision oncology and, in many cases, tumour genomic profiling at progression is not possible due to technical limitations of obtaining new tumour tissue specimens. Efficient diagnostic alternatives are therefore required for molecular stratification, which includes liquid biopsy. This technique enables the evaluation of the tumour genomic profile dynamically and captures intra-patient genomic heterogeneity as well. To date, there are several diagnostic techniques available for use in liquid biopsy, each one of them with different precision and performance levels. The objective of this consensus statement of the Spanish Society of Pathology and the Spanish Society of Medical Oncology is to evaluate the viability and effectiveness of the different methodological approaches in liquid biopsy in cancer patients and the potential application of this method to current clinical practice. The experts contributing to this consensus statement agree that, according to current evidence, liquid biopsy is an acceptable alternative to tumour tissue biopsy for the study of biomarkers in various clinical settings. It is therefore important to standardise pre-analytical and analytical procedures, to ensure reproducibility and generate structured and accessible clinical reports. It is essential to appoint multidisciplinary tumour molecular boards to oversee these processes and to enable the most suitable therapeutic decisions for each patient according to the genomic profile.

Idioma: Inglés

DOI: 10.1007/s12094-019-02211-x

Año: 2020

Publicado en: Clinical and Translational Oncology 22, 6 (2020), 823-834
ISSN: 1699-048X

Factor impacto JCR: 3.405 (2020)

Categ. JCR: ONCOLOGY rank: 159 / 242 = 0.657 (2020) - Q3 - T2

Factor impacto SCIMAGO: 0.902 - Cancer Research (Q2) - Oncology (Q2) - Medicine (miscellaneous) (Q2)

Tipo y forma: Article (Published version)

Área (Departamento): Area Anatom.Embriol.Humana (Dpto. Anatom.Histolog.Humanas)