Multicentric Longitudinal Performance Monitoring of Different Prenatal Cell‐Free DNA Screening Technologies in Belgium
OBJECTIVE: Prenatal cell-free DNA screening is widely used to assess the risk of fetal trisomy 21, 18, and 13. Although commercial and laboratory-developed tests (LDTs) show high accuracy in validation studies, real-world longitudinal performance data are lacking. METHOD: In Belgium, prenatal cell-free DNA screening is a population screening offered to all pregnant people, regardless of their a priori risk. Over 3 years, all confirmatory diagnostic tests after a positive prenatal cell-free DNA screening result were recorded along with the technologies used and their outcomes. Positive predictive values (PPVs) for the three common fetal trisomies were calculated per technology. RESULTS: A total of 1158 diagnostic tests were performed after a positive prenatal cell-free DNA screening. Of these, 58.5% came from an LDT, 15.7% from VeriSeq (Illumina), 6.6% from Harmony (Roche), 5% from Vanadis (Perkin-Elmer); for 14.2% the technology could not be traced. PPVs ranged from 92.2% to 65.7% for trisomy 21, from 82.8% to 44.4% for trisomy 18, and from 40% to 18.2% for trisomy 13. Overall, the LDT performed better than the commercial tests. CONCLUSION: This study confirms the reported accuracy of commercial tests and LDT, while showing that LDT generally outperforms commercial tests. Despite high specificities across tests, differences in PPVs significantly impact pregnant people and the national health care system.
Authors
- Kim Van Berkel (ORCID: https://orcid.org/0000-0002-6940-7509)
- Machteld Baetens (ORCID: https://orcid.org/0000-0001-7573-1164)
- Marie Bruneau (ORCID: https://orcid.org/0000-0003-3746-5752)
- Ann Van Den Bogaert (ORCID: https://orcid.org/0000-0003-2523-0702)
- Armelle Duquenne
- Jean‐Stéphane Gatot
- Leen Vancoillie
- Katrien Janssens (ORCID: https://orcid.org/0000-0002-3249-731X)
- Olivier Vanakker
- Bettina Blaumeiser (ORCID: https://orcid.org/0000-0001-9993-7319)
- Bruno Pichon (ORCID: https://orcid.org/0000-0001-7973-3781)
- Angelica Pagliazzi (ORCID: https://orcid.org/0000-0002-9128-6264)
- Axel Marichal
- Isabelle Vandernoot (ORCID: https://orcid.org/0000-0001-8084-7858)
- Lore Lannoo (ORCID: https://orcid.org/0000-0002-6271-221X)
- Marjan De Rademaeker
- Björn Menten (ORCID: https://orcid.org/0000-0001-8182-659X)
- Sandra Coppens (ORCID: https://orcid.org/0000-0001-9155-7506)
- Sandra Janssens (ORCID: https://orcid.org/0000-0001-7262-3715)
- Ilse Parijs
- S. Rombout (ORCID: https://orcid.org/0000-0003-2479-3204)
- Colombine Meunier (ORCID: https://orcid.org/0009-0000-7807-8594)
- Koenraad Devriendt (ORCID: https://orcid.org/0000-0002-3651-2548)
- Ileen Slegers (ORCID: https://orcid.org/0000-0001-5907-829X)
- Nathalie Brison
- Yves Sznajer (ORCID: https://orcid.org/0000-0001-8161-4490)
- Annelies Fieuw
- Julie Désir (ORCID: https://orcid.org/0000-0002-1998-0761)
- Saskia Bulk (ORCID: https://orcid.org/0009-0002-3763-7964)
- Kris Van Den Bogaert (ORCID: https://orcid.org/0000-0003-4525-5907)
- Mauricette Jamar
- Joris R. Vermeesch
- Bert Callewaert
- Anne De Leener
- Michelle DEBERG
Institutions
- Cliniques Universitaires Saint-Luc (BE)
- University of Liège (BE)
- Ghent University Hospital (BE)
- Erasmus Hospital (BE)
- Institute of Pathology and Genetics (BE)
- Antwerp University Hospital (BE)
- Center for Human Genetics (US)
- Centre Hospitalier Universitaire de Liège (BE)
Publication Details
- Journal
- Prenatal Diagnosis
- Published
- 2026-08-17
- DOI
- https://doi.org/10.1002/pd.70236
- Primary Topic
- Prenatal Screening and Diagnostics
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- KU Leuven