Challenges and opportunities for cancer predisposition cascade screening for hereditary breast and ovarian cancer and lynch syndrome in Switzerland : findings from an international workshop

Nikolaidis, Christos; Ming, Chang; Pedrazzani, Carla; van der Horst, Tina; Kaiser-Grolimund, Andrea; Ademi, Zanfina; Bührer-Landolt, Rosmarie; Bürki, Nicole; Caiata-Zufferey, Maria; Champion, Victoria; Chappuis, Pierre O.; Kohler, Carmen; Erlanger, Tobias E.; Graffeo, Rossella; Hampel, Heather; Heinimann, Karl; Heinzelmann-Schwarz, Viola; Kurzeder, Christian; Monnerat, Christian; Northouse, Laurel L.; Pagani, Olivia; Probst-Hensch, Nicole; Rabaglio, Manuela; Schoenau, Eveline; Sijbrands, Eric J.G.; Taborelli, Monika; Urech, Corinne; Viassolo, Valeria; Wieser, Simon; Katapodi, Maria C.

doi:10.1159/000496495

Publication type:	Article in scientific journal
Type of review:	Peer review (publication)
Title:	Challenges and opportunities for cancer predisposition cascade screening for hereditary breast and ovarian cancer and lynch syndrome in Switzerland : findings from an international workshop
Authors:	Nikolaidis, Christos Ming, Chang Pedrazzani, Carla van der Horst, Tina Kaiser-Grolimund, Andrea Ademi, Zanfina Bührer-Landolt, Rosmarie Bürki, Nicole Caiata-Zufferey, Maria Champion, Victoria Chappuis, Pierre O. Kohler, Carmen Erlanger, Tobias E. Graffeo, Rossella Hampel, Heather Heinimann, Karl Heinzelmann-Schwarz, Viola Kurzeder, Christian Monnerat, Christian Northouse, Laurel L. Pagani, Olivia Probst-Hensch, Nicole Rabaglio, Manuela Schoenau, Eveline Sijbrands, Eric J.G. Taborelli, Monika Urech, Corinne Viassolo, Valeria Wieser, Simon Katapodi, Maria C.
et. al:	No
DOI:	10.1159/000496495
Published in:	Public Health Genomics
Volume(Issue):	21
Issue:	3-4
Page(s):	121
Pages to:	132
Issue Date:	2019
Publisher / Ed. Institution:	Karger
ISSN:	1662-4246 1662-8063
Language:	English
Subjects:	Cascade genetic screening; Hereditary breast and ovarian cancer; Implementation science; Lynch syndrome; Public health genetics; Breast Neoplasms; Carcinoma, Ovarian Epithelial; Colorectal Neoplasms, Hereditary Nonpolyposis; Cost-Benefit Analysis; Early Detection of Cancer; Female; Humans; Ovarian Neoplasms; Social Support; Switzerland; Genetic Predisposition to Disease; Genetic Testing; Internationality
Subject (DDC):	614: Public health and prevention of disease 616: Internal medicine and diseases
Abstract:	An international workshop on cancer predisposition cascade genetic screening for hereditary breast and ovarian cancer (HBOC) and Lynch syndrome (LS) took place in Switzerland, with leading researchers and clinicians in cascade screening and hereditary cancer from different disciplines. The purpose of the workshop was to enhance the implementation of cascade genetic screening in Switzerland. Participants discussed the challenges and opportunities associated with cascade screening for HBOC and LS in Switzerland (CASCADE study); family implications and the need for family-based interventions; the need to evaluate the cost-effectiveness of cascade genetic screening; and interprofessional collaboration needed to lead this initiative.
URI:	https://digitalcollection.zhaw.ch/handle/11475/22195
Fulltext version:	Published version
License (according to publishing contract):	Licence according to publishing contract
Departement:	School of Management and Law
Organisational Unit:	Winterthur Institute of Health Economics (WIG)
Appears in collections:	Publikationen School of Management and Law

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Nikolaidis, C., Ming, C., Pedrazzani, C., van der Horst, T., Kaiser-Grolimund, A., Ademi, Z., Bührer-Landolt, R., Bürki, N., Caiata-Zufferey, M., Champion, V., Chappuis, Pierre O., Kohler, C., Erlanger, Tobias E., Graffeo, R., Hampel, H., Heinimann, K., Heinzelmann-Schwarz, V., Kurzeder, C., Monnerat, C., et al. (2019). Challenges and opportunities for cancer predisposition cascade screening for hereditary breast and ovarian cancer and lynch syndrome in Switzerland : findings from an international workshop. Public Health Genomics, 21(3-4), 121–132. https://doi.org/10.1159/000496495

Nikolaidis, C. et al. (2019) ‘Challenges and opportunities for cancer predisposition cascade screening for hereditary breast and ovarian cancer and lynch syndrome in Switzerland : findings from an international workshop’, Public Health Genomics, 21(3-4), pp. 121–132. Available at: https://doi.org/10.1159/000496495.

C. Nikolaidis et al., “Challenges and opportunities for cancer predisposition cascade screening for hereditary breast and ovarian cancer and lynch syndrome in Switzerland : findings from an international workshop,” Public Health Genomics, vol. 21, no. 3-4, pp. 121–132, 2019, doi: 10.1159/000496495.

NIKOLAIDIS, Christos, Chang MING, Carla PEDRAZZANI, Tina VAN DER HORST, Andrea KAISER-GROLIMUND, Zanfina ADEMI, Rosmarie BÜHRER-LANDOLT, Nicole BÜRKI, Maria CAIATA-ZUFFEREY, Victoria CHAMPION, Pierre O. CHAPPUIS, Carmen KOHLER, Tobias E. ERLANGER, Rossella GRAFFEO, Heather HAMPEL, Karl HEINIMANN, Viola HEINZELMANN-SCHWARZ, Christian KURZEDER, Christian MONNERAT, Laurel L. NORTHOUSE, Olivia PAGANI, Nicole PROBST-HENSCH, Manuela RABAGLIO, Eveline SCHOENAU, Eric J.G. SIJBRANDS, Monika TABORELLI, Corinne URECH, Valeria VIASSOLO, Simon WIESER und Maria C. KATAPODI, 2019. Challenges and opportunities for cancer predisposition cascade screening for hereditary breast and ovarian cancer and lynch syndrome in Switzerland : findings from an international workshop. Public Health Genomics. 2019. Bd. 21, Nr. 3-4, S. 121–132. DOI 10.1159/000496495

Nikolaidis, Christos, Chang Ming, Carla Pedrazzani, Tina van der Horst, Andrea Kaiser-Grolimund, Zanfina Ademi, Rosmarie Bührer-Landolt, et al. 2019. “Challenges and Opportunities for Cancer Predisposition Cascade Screening for Hereditary Breast and Ovarian Cancer and Lynch Syndrome in Switzerland : Findings from an International Workshop.” Public Health Genomics 21 (3-4): 121–32. https://doi.org/10.1159/000496495.

Nikolaidis, Christos, et al. “Challenges and Opportunities for Cancer Predisposition Cascade Screening for Hereditary Breast and Ovarian Cancer and Lynch Syndrome in Switzerland : Findings from an International Workshop.” Public Health Genomics, vol. 21, no. 3-4, 2019, pp. 121–32, https://doi.org/10.1159/000496495.