| Literature DB >> 26355862 |
Frédéric Amant1, Magali Verheecke1, Iwona Wlodarska2, Luc Dehaspe2, Paul Brady2, Nathalie Brison2, Kris Van Den Bogaert2, Daan Dierickx3, Vincent Vandecaveye4, Thomas Tousseyn5, Philippe Moerman5, Adriaan Vanderstichele2, Ignace Vergote2, Patrick Neven2, Patrick Berteloot6, Katrien Putseys7, Lode Danneels8, Peter Vandenberghe9, Eric Legius2, Joris Robert Vermeesch2.
Abstract
IMPORTANCE: Noninvasive prenatal testing (NIPT) for fetal aneuploidy by scanning cell-free fetal DNA in maternal plasma is rapidly becoming a major prenatal genetic test. Similar to placental DNA, tumor DNA can be detected in the plasma, and analysis of cell-free tumor DNA can be used to characterize and monitor cancers. We show that plasma DNA profiling allows for presymptomatic detection of tumors in pregnant women undergoing routine NIPT. OBSERVATIONS: During NIPT in over 4000 prospective pregnancies by parallel sequencing of maternal plasma cell-free DNA, 3 aberrant genome representation (GR) profiles were observed that could not be attributed to the maternal or fetal genomic constitution. A maternal cancer was suspected, and those 3 patients were referred for whole-body diffusion-weighted magnetic resonance imaging, which uncovered an ovarian carcinoma, a follicular lymphoma, and a Hodgkin lymphoma, each confirmed by subsequent pathologic and genetic investigations. The copy number variations in the subsequent tumor biopsies were concordant with the NIPT plasma GR profiles. CONCLUSIONS AND RELEVANCE: We show that maternal plasma cell-free DNA sequencing for noninvasive prenatal testing also may enable accurate presymptomatic detection of maternal tumors and treatment during pregnancy.Entities:
Mesh:
Substances:
Year: 2015 PMID: 26355862 DOI: 10.1001/jamaoncol.2015.1883
Source DB: PubMed Journal: JAMA Oncol ISSN: 2374-2437 Impact factor: 31.777