“I just wanted more”: Hereditary cancer syndromes patients’ perspectives on the utility of circulating tumour DNA testing for cancer screening
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Published:2023-10-11
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Volume:
Page:
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ISSN:1018-4813
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Container-title:European Journal of Human Genetics
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language:en
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Short-container-title:Eur J Hum Genet
Author:
Adi-Wauran Ella, Clausen Marc, Shickh Salma, Gagliardi Anna R., Denburg Avram, Oldfield Leslie E., Sam Jordan, Reble Emma, Krishnapillai Suvetha, Regier Dean A.ORCID, Baxter Nancy N., Dawson Lesa, Penney Lynette S., Foulkes WilliamORCID, Basik Mark, Sun Sophie, Schrader Kasmintan A.ORCID, Karsan AlyORCID, Pollett Aaron, Pugh Trevor J., Dawson Lesa, Rideout Krista, Whittle Stacy, Penney Lynette S., Wallace Karin, MacDonald Shelley M., Basik Mark, Foulkes William, Aguilar-Mahecha Adriana, Rezoug Zoulikha, Carile Victoria, Lafleur Josiane, Bombard Yvonne, Baxter Nancy N., Dhalla Irfan, Mckee Brian, Mittmann Nicole, Kastner Monika, Jacobson Michelle R., Bernardini Marcus Q., Ene Gabrielle E. V., Kim Raymond H., Pugh Trevor J., Oldfield Leslie E., Farncombe Kirsten M., Siu Lillian, Lheureux Stephanie, Ferguson Sarah, Elser Christine, Cil Tulin, Westergard Shelley, Thain Emily, Berman Hal, Xu Wei, Yu Celeste, Norman Maia L., Chan Clarissa F., Uju Precious, Bedard Phil, Clarke Blaise, McCuaig Jeanna, Pollett Aaron, Aronson Melyssa, Gryfe Robert, Panchal Seema, Piccinin Carolyn, Ward Thomas, Semotiuk Kara, Lerner-Ellis Jordan, Regier Dean, Karsan Aly, Schrader Kasmintan A., Kaurah Pardeep, Sun Sophie, Singh Sara, Kim Raymond H.ORCID, Bombard YvonneORCID,
Funder
Gouvernement du Canada | Canadian Institutes of Health Research Princess Margaret Cancer Foundation
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference33 articles.
1. Garber JE, Offit K. Hereditary cancer predisposition syndromes. J Clin Oncol. 2005;23:276–92. https://doi.org/10.1200/JCO.2005.10.042 2. Petrucelli N, Daly MB, Pal T BRCA1- and BRCA2-Associated Hereditary Breast and Ovarian Cancer. GeneReviews. Published online 2022:1–37. 3. Dominguez-Valentin M, Sampson JR, Seppälä TT, Ten Broeke SW, Plazzer JP, Nakken S, et al. Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database. Genet Med. 2020;22:15–25. https://doi.org/10.1038/s41436 4. Barrow E, Hill J, Gareth D. Cancer risk in Lynch Syndrome. Fam Cancer. 2013;12:229–40. https://doi.org/10.1007/s10689-013-9615-1 5. Rabeneck L, Paszat LF, Saskin R, Stukel TA. Association between colonoscopy rates and colorectal cancer mortality. Am J Gastroenterol. 2010:1–6. https://doi.org/10.1038/ajg.2010.83
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