JAMA oncology · 2015
Presymptomatic Identification of Cancers in Pregnant Women During Noninvasive Prenatal Testing.
Клинический случайСтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод пока не подготовлен
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Amant Frédéric, Verheecke Magali, Wlodarska Iwona, Dehaspe Luc, Brady Paul, Brison Nathalie, Van Den Bogaert Kris, Dierickx Daan, Vandecaveye Vincent, Tousseyn Thomas, Moerman Philippe, Vanderstichele Adriaan, Vergote Ignace, Neven Patrick, Berteloot Patrick, Putseys Katrien, Danneels Lode, Vandenberghe Peter, Legius Eric, Vermeesch Joris Robert
Аннотация
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.
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.
Предметные рубрики MeSH
Asymptomatic DiseasesBiomarkers, TumorBiopsyDNA, NeoplasmDiffusion Magnetic Resonance ImagingFemaleGene Expression ProfilingGenetic Predisposition to DiseaseGenetic TestingHodgkin DiseaseHumansIn Situ Hybridization, FluorescenceLymphoma, FollicularOvarian NeoplasmsPhenotypePredictive Value of TestsPregnancyPregnancy Complications, NeoplasticPrenatal DiagnosisPrognosisWhole Body Imaging