Liquid Biopsy for Biomarker Testing in Non-Small Cell Lung Cancer: A European Perspective
Metadatos
Mostrar el registro completo del ítemAutor
Malapelle, Umberto; Tiseo, Marcello; Vivancos, Ana; Kapp, Joshua; Serrano Fernández, María José; Tiemann, MarkusEditorial
MDPI
Materia
cfDNA ctDNA liquid biopsy
Fecha
2021-08-18Referencia bibliográfica
Malapelle, U. et. al. J. Mol. Pathol. 2021, 2, 255–273. [https://doi.org/10.3390/jmp2030022]
Patrocinador
Amgen (Europe) GmbH (Rotkreuz, Switzerland)Resumen
The development of targeted therapies has improved survival rates for patients with
advanced non-small cell lung cancer (NSCLC). However, tissue biopsy is unfeasible or inadequate in
many patients, limiting biomarker testing and access to targeted therapies. The increasing numbers of
established and emerging biomarkers with available targeted treatments highlights the challenges associated
with sequential single-gene testing and limited tissue availability. Multiplex next-generation
sequencing (NGS) offers an attractive alternative and represents a logical next step, and in cases
where the tumour is inaccessible, tissue biopsy yields insufficient tumour content, or when the patient’s
performance status does not allow a tissue biopsy, liquid biopsy can provide valuable material
for molecular diagnosis. Here, we explore the role of liquid biopsy (i.e., circulating cell-free DNA
analysis) in Europe. Liquid biopsies could be used as a complementary approach to increase rates
of molecular diagnosis, with the ultimate aim of improving patient access to appropriate targeted
therapies. Expert opinion is also provided on potential future applications of liquid biopsy in NSCLC,
including for cancer prevention, detection of early stage and minimum residual disease, monitoring
of response to therapy, selection of patients for immunotherapy, and monitoring of tumour evolution
to enable optimal adaptation/combination of drug therapies.