Literature DB >> 27878832

Prenatal cfDNA screening results indicative of maternal neoplasm: survey of current practice and management needs.

Meagan E Giles1, Lauren Murphy1,2, Nevena Krstić1,2, Cathy Sullivan3, Syed S Hashmi4, Blair Stevens1,2.   

Abstract

OBJECTIVE: To determine genetic counselors' current practices and management needs for patients with prenatal cfDNA screening results indicative of maternal neoplasm.
METHODS: A survey was completed by genetic counselors recruited via the National Society of Genetic Counselors (NSGC).
RESULTS: Over 300 genetic counselors were surveyed. Almost all participants (95%) were aware that Noninvasive Prenatal Testing (NIPT) results may suggest maternal neoplasm, and 77% reported they would disclose such results. However, only 29% routinely communicate this possibility to patients in a pre-test setting. Management recommendations made by counselors were highly variable, and over half (51.8%) stated they would feel uncomfortable or very uncomfortable counseling a patient with these results. While less than half (44.3%) believed the current benefits of NIPT's ability to suggest maternal neoplasm outweigh its potential harms, 80.2% recognized it would be beneficial in the future. A vast majority of counselors (91.3%) felt institutional or national guidelines were needed for patient management.
CONCLUSION: A majority of counselors neither felt properly equipped nor comfortable counseling patients with prenatal cfDNA results suggestive of maternal neoplasm. This study demonstrates a need for collaboration amongst clinicians, researchers, and laboratories to publish data regarding NIPT results indicative of maternal neoplasm, and for the creation of management guidelines.
© 2016 John Wiley & Sons, Ltd. © 2016 John Wiley & Sons, Ltd.

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Year:  2016        PMID: 27878832     DOI: 10.1002/pd.4973

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  5 in total

1.  Current Controversies in Prenatal Diagnosis 2: NIPT results suggesting maternal cancer should always be disclosed.

Authors:  Peter Benn; Sharon E Plon; Diana W Bianchi
Journal:  Prenat Diagn       Date:  2018-12-10       Impact factor: 3.050

2.  Genetic Counselors' Perspectives About Cell-Free DNA: Experiences, Challenges, and Expectations for Obstetricians.

Authors:  Patricia K Agatisa; Mary Beth Mercer; Marissa Coleridge; Ruth M Farrell
Journal:  J Genet Couns       Date:  2018-06-27       Impact factor: 2.537

3.  Prenatal DNA Sequencing for Fetal Aneuploidy Also Detects Maternal Cancer: Importance of Timely Workup and Management in Pregnant Women.

Authors:  Amy E Turriff; Christina M Annunziata; Diana W Bianchi
Journal:  J Clin Oncol       Date:  2022-06-15       Impact factor: 50.717

4.  Comprehensive genome-wide analysis of routine non-invasive test data allows cancer prediction: A single-center retrospective analysis of over 85,000 pregnancies.

Authors:  Liesbeth Lenaerts; Nathalie Brison; Charlotte Maggen; Leen Vancoillie; Huiwen Che; Peter Vandenberghe; Daan Dierickx; Lucienne Michaux; Barbara Dewaele; Patrick Neven; Giuseppe Floris; Thomas Tousseyn; Lore Lannoo; Tatjana Jatsenko; Isabelle Vanden Bempt; Kristel Van Calsteren; Vincent Vandecaveye; Luc Dehaspe; Koenraad Devriendt; Eric Legius; Kris Van Den Bogaert; Joris Robert Vermeesch; Frédéric Amant
Journal:  EClinicalMedicine       Date:  2021-05-13

5.  Identification of Structural Variation from NGS-Based Non-Invasive Prenatal Testing.

Authors:  Ondrej Pös; Jaroslav Budis; Zuzana Kubiritova; Marcel Kucharik; Frantisek Duris; Jan Radvanszky; Tomas Szemes
Journal:  Int J Mol Sci       Date:  2019-09-07       Impact factor: 5.923

  5 in total

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