Assessment of Pre-Analytical Sample Handling Conditions for Comprehensive Liquid Biopsy Analysis.
Adolescent
Adult
Aged
Blood Donors
Blood Specimen Collection
/ methods
Circulating Tumor DNA
/ genetics
Diagnostic Tests, Routine
/ methods
Edetic Acid
/ chemistry
Feasibility Studies
Female
Flow Cytometry
/ methods
Genetic Testing
/ methods
Heparin
/ chemistry
Humans
Leukocytes
Liquid Biopsy
/ methods
Male
Middle Aged
Molecular Diagnostic Techniques
/ methods
Phenotype
Temperature
Time Factors
Whole Genome Sequencing
/ methods
Young Adult
Journal
The Journal of molecular diagnostics : JMD
ISSN: 1943-7811
Titre abrégé: J Mol Diagn
Pays: United States
ID NLM: 100893612
Informations de publication
Date de publication:
08 2020
08 2020
Historique:
received:
12
06
2019
revised:
05
05
2020
accepted:
19
05
2020
pubmed:
5
6
2020
medline:
28
8
2021
entrez:
5
6
2020
Statut:
ppublish
Résumé
Liquid biopsies as a minimally invasive approach have the potential to revolutionize molecular diagnostics. Yet, although protocols for sample handling and the isolation of circulating tumor DNA (ctDNA) are numerous, comprehensive guidelines for diagnostics and research considering all aspects of real-life multicenter clinical studies are currently not available. These include limitations in sample volume, transport, and blood collection tubes. We tested the impact of commonly used (EDTA and heparin) and specialized blood collection tubes and storage conditions on the yield and purity of cell-free DNA for the application in down-stream analysis. Moreover, we evaluated the feasibility of a combined workflow for ctDNA and tumor cell genomic testing and parallel flow cytometric analysis of leukocytes. For genomic analyses, EDTA tubes showed good results if stored for a maximum of 4 hours at room temperature or for up to 24 hours when stored at 4°C. Spike-in experiments revealed that EDTA tubes in combination with density gradient centrifugation allowed the parallel isolation of ctDNA, leukocytes, and low amounts of tumor cells (0.1%) and their immunophenotyping by flow cytometry and down-stream genomic analysis by whole genome sequencing. In conclusion, adhering to time and temperature limits allows the use of routine EDTA blood samples for liquid biopsy analyses. We further provide a workflow enabling the parallel analysis of cell-free and cellular features for disease monitoring and for clonal evolution studies.
Identifiants
pubmed: 32497717
pii: S1525-1578(20)30351-2
doi: 10.1016/j.jmoldx.2020.05.006
pii:
doi:
Substances chimiques
Circulating Tumor DNA
0
Heparin
9005-49-6
Edetic Acid
9G34HU7RV0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1070-1086Subventions
Organisme : Austrian Science Fund FWF
ID : I 4162
Pays : Austria
Informations de copyright
Copyright © 2020 Association for Molecular Pathology and American Society for Investigative Pathology. Published by Elsevier Inc. All rights reserved.