Pre-Analytical Evaluation of Streck Cell-Free DNA Blood Collection Tubes for Liquid Profiling in Oncology

Author:

Diaz Inga Medina1,Nocon Annette1,Held Stefanie A. E.2,Kobilay Makbule3,Skowasch Dirk4,Bronkhorst Abel J.5,Ungerer Vida5,Fredebohm Johannes1,Diehl Frank1,Holdenrieder Stefan35ORCID,Holtrup Frank1

Affiliation:

1. Research and Development, Sysmex Inostics GmbH, 20251 Hamburg, Germany

2. Department of Hematology and Oncology, University Hospital, 53127 Bonn, Germany

3. Institute of Clinical Chemistry and Clinical Pharmacology, University Hospital, 53127 Bonn, Germany

4. Department of Pneumology, University Hospital, 53127 Bonn, Germany

5. German Heart Centre Munich, Institute for Laboratory Medicine, Technical University, 80636 Munich, Germany

Abstract

Excellent pre-analytical stability is an essential precondition for reliable molecular profiling of circulating tumor DNA (ctDNA) in oncological diagnostics. Therefore, in vitro degradation of ctDNA and the additional release of contaminating genomic DNA from lysed blood cells must be prevented. Streck Cell-Free DNA blood collection tubes (cfDNA BCTs) have proposed advantages over standard K2EDTA tubes, but mainly have been tested in healthy individuals. Blood was collected from cancer patients (n = 53) suffering from colorectal (n = 21), pancreatic (n = 11), and non-small-cell lung cancer (n = 21) using cfDNA BCT tubes and K2EDTA tubes that were processed immediately or after 3 days (BCTs) or 6 hours (K2EDTA) at room temperature. The cfDNA isolated from these samples was characterized in terms of yield using LINE-1 qPCR; the level of gDNA contamination; and the mutation status of KRAS, NRAS, and EGFR genes using BEAMing ddPCR. CfDNA yield and gDNA levels were comparable in both tube types and were not affected by prolonged storage of blood samples for at least 3 days in cfDNA BCTs or 6 hours in K2EDTA tubes. In addition, biospecimens collected in K2EDTA tubes and cfDNA BCTs stored for up to 3 days demonstrated highly comparable levels of mutational load across all respective cancer patient cohorts and a wide range of concentrations. Our data support the applicability of clinical oncology specimens collected and stored in cfDNA BCTs for up to 3 days for reliable cfDNA and mutation analyses.

Funder

Sysmex Inostics GmbH

Publisher

MDPI AG

Subject

Clinical Biochemistry

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