دورية أكاديمية

Clinical practice guidelines for the diagnosis and surveillance of BAP1 tumour predisposition syndrome

التفاصيل البيبلوغرافية
العنوان: Clinical practice guidelines for the diagnosis and surveillance of BAP1 tumour predisposition syndrome
المؤلفون: Lalloo, Fiona, Kulkarni, Anju, Chau, Cindy, Nielsen, Maartje, Sheaff, Michael, Steele, Jeremy, van Doorn, Remco, Wadt, Karin, Hamill, Monica, Torr, Beth, Tischkowitz, Marc, Ahmed, Munaza, Bajalica-Lagercrantz, Svetlana, Blatnik, Ana, Brunet, Joan, Cleaver, Ruth, Colas, Chrystelle, Dabir, Tabib, Evans, D. Gareth, Feshtali, Shirin, Ghiorzo, Paola, Graversen, Lise, Griewank, Klaus, Helgadottir, Hildur, Jewell, Rosalyn, Kohut, Kelly, Lorentzen, Henrik, Massi, Daniela, Missotten, Guy, Murray, Alex, Murray, Jennie, Nadal, Ernest, Ong, Kai Ren, Piulats, Josep M., Puig, Susana, Rajan, Neil, Ribero, Simone, Salle, Galateau, Teulé, Alexandre, Tham, Emma, van Paassen, Barbara, De Putter, Robin, Verdijk, Robert, Wagner, Anja, Woodward, Emma R., Hanson, Helen
المصدر: Lalloo , F , Kulkarni , A , Chau , C , Nielsen , M , Sheaff , M , Steele , J , van Doorn , R , Wadt , K , Hamill , M , Torr , B , Tischkowitz , M , Ahmed , M , Bajalica-Lagercrantz , S , Blatnik , A , Brunet , J , Cleaver , R , Colas , C , Dabir , T , Evans , D G , Feshtali , S , Ghiorzo , P , Graversen , L , Griewank , K , Helgadottir , H , Jewell ....
سنة النشر: 2023
مصطلحات موضوعية: /dk/atira/pure/sustainabledevelopmentgoals/good_health_and_well_being, name=SDG 3 - Good Health and Well-being
الوصف: BRCA1-associated protein-1 (BAP1) is a recognised tumour suppressor gene. Germline BAP1 pathogenic/likely pathogenic variants are associated with predisposition to multiple tumours, including uveal melanoma, malignant pleural and peritoneal mesothelioma, renal cell carcinoma and specific non-malignant neoplasms of the skin, as part of the autosomal dominant BAP1-tumour predisposition syndrome. The overall lifetime risk for BAP1 carriers to develop at least one BAP1-associated tumour is up to 85%, although due to ascertainment bias, current estimates of risk are likely to be overestimated. As for many rare cancer predisposition syndromes, there is limited scientific evidence to support the utility of surveillance and, therefore, management recommendations for BAP1 carriers are based on expert opinion. To date, European recommendations for BAP1 carriers have not been published but are necessary due to the emerging phenotype of this recently described syndrome and increased identification of BAP1 carriers via large gene panels or tumour sequencing. To address this, the Clinical Guideline Working Group of the CanGene-CanVar project in the United Kingdom invited European collaborators to collaborate to develop guidelines to harmonize surveillance programmes within Europe. Recommendations with respect to BAP1 testing and surveillance were achieved following literature review and Delphi survey completed by a core group and an extended expert group of 34 European specialists including Geneticists, Ophthalmologists, Oncologists, Dermatologists and Pathologists. It is recognised that these largely evidence-based but pragmatic recommendations will evolve over time as further data from research collaborations informs the phenotypic spectrum and surveillance outcomes.
نوع الوثيقة: article in journal/newspaper
وصف الملف: application/pdf
اللغة: English
العلاقة: https://pure.eur.nl/en/publications/a3e5a976-36fb-40d0-894f-88195dcdc2d3Test
DOI: 10.1038/s41431-023-01448-z
الإتاحة: https://doi.org/10.1038/s41431-023-01448-zTest
https://pure.eur.nl/en/publications/a3e5a976-36fb-40d0-894f-88195dcdc2d3Test
https://pure.eur.nl/ws/files/99627608/Clinical_practice_guidelines_for_the_diagnosis_and_surveillance_of_BAP1_tumour_predisposition_syndrome.pdfTest
http://www.scopus.com/inward/record.url?scp=85168608297&partnerID=8YFLogxKTest
حقوق: info:eu-repo/semantics/openAccess
رقم الانضمام: edsbas.D8A94AD9
قاعدة البيانات: BASE