| Literature DB >> 28958829 |
Karin Birkenkamp-Demtröder1, Emil Christensen2, Iver Nordentoft2, Michael Knudsen3, Ann Taber2, Søren Høyer4, Philippe Lamy2, Mads Agerbæk5, Jørgen Bjerggaard Jensen6, Lars Dyrskjøt7.
Abstract
Of the patients undergoing radical cystectomy, 20-80% experience relapse. Minimally invasive methods for early detection of metastatic relapse after cystectomy and for monitoring ongoing therapy are urgently needed to improve individualised follow-up and treatment. Therefore, we evaluated the use of circulating tumour DNA (ctDNA) in plasma and urine to detect metastatic relapse after cystectomy and measure treatment efficacy. We exome sequenced tumour and germline DNA from patients with muscle-invasive bladder cancer and monitored ctDNA in 370 liquid biopsies throughout the disease courses by 84 personalised digital droplet polymerase chain reaction assays targeting 61 genes. Patients were prospectively recruited between 2013 and 2017. Patients with metastatic relapse had significantly higher ctDNA levels compared with disease-free patients (p<0.001). The median positive lead time between ctDNA detection in plasma and diagnosis of relapse was 101 d after cystectomy (range 0-932 d). Early detection of metastatic relapse and treatment response using liquid biopsies represents a novel, highly sensitive tool for monitoring patients, supporting clinicians, and guiding treatment decisions. PATIENTEntities:
Keywords: Biomarker; Cell-free DNA; Droplet digital polymerase chain reaction; Liquid biopsy; Minimally invasive monitoring; Neoadjuvant chemotherapy; Personalised analysis; Plasma; Reservoir urine; Treatment response
Mesh:
Substances:
Year: 2017 PMID: 28958829 DOI: 10.1016/j.eururo.2017.09.011
Source DB: PubMed Journal: Eur Urol ISSN: 0302-2838 Impact factor: 20.096