scholarly journals Linking population‐based registries to identify familial cancer risk in childhood cancer

Cancer ◽  
2020 ◽  
Vol 126 (13) ◽  
pp. 3076-3083 ◽  
Author(s):  
Laura‐Maria Madanat‐Harjuoja ◽  
Janne Pitkäniemi ◽  
Elli Hirvonen ◽  
Nea Malila ◽  
Lisa R. Diller
Keyword(s):  
Cancer Risk ◽  
Childhood Cancer ◽  
Familial Cancer ◽  
Population Based ◽  
Familial Cancer Risk

scholarly journals Psoriasis vulgaris and familial cancer risk- a population-based study

2013 ◽  
Vol 11 (1) ◽  
Author(s):  
Romuald Maleszka ◽  
Katarzyna Paszkowska-Szczur ◽  
Ewa Soczawa ◽  
Magdalena Boer ◽  
Monika Różewicka-Czabańska ◽  
...  
Keyword(s):  
Cancer Risk ◽  
Psoriasis Vulgaris ◽  
Familial Cancer ◽  
Population Based ◽  
Population Based Study ◽  
Familial Cancer Risk

scholarly journals Recommendation and Acceptance of Counselling for Familial Cancer Risk in Newly Diagnosed Breast Cancer Cases

Breast Care ◽  
2021 ◽  
pp. 1-6
Author(s):  
Karin Kast ◽  
Julia Häfner ◽  
Evelin Schröck ◽  
Arne Jahn ◽  
Carmen Werner ◽  
...  
Keyword(s):  
Breast Cancer ◽  
Cancer Risk ◽  
Genetic Counselling ◽  
Primary Breast Cancer ◽  
Ductal Carcinoma ◽  
Familial Cancer ◽  
University Hospital ◽  
Tumor Board ◽  
Newly Diagnosed ◽  
Familial Cancer Risk

<b><i>Background:</i></b> In clinical routine, not every patient who is offered genetic counselling and diagnostics in order to investigate a familial cancer risk predisposition opts for it. Little is known about acceptance of counselling and testing in newly diagnosed breast cancer cases in Germany. <b><i>Methods:</i></b> All primary breast cancer cases and patients with DCIS (ductal carcinoma in situ) treated at the University Hospital of Dresden between 2016 and 2019 were included. The number of tumor board recommendations for genetic counselling on the basis of the GC-HBOC risk criteria was recorded. Acceptance was analyzed by number of cases with counselling in the GC-HBOC-Center Dresden. <b><i>Results:</i></b> Of 996 primary breast cancer and DCIS cases, 262 (26.3%) were eligible for genetic counselling. Recommendation for genetic counselling was accepted by 64.1% (168/262). Of these 90.5% (152/168) opted for molecular genetic analysis. The acceptance rate for counselling increased between 2016 and 2019 from 58.3 to 72.6%. Altogether, 20.4% (31/152) patients were found to carry a pathogenic variant in the breast cancer genes <i>BRCA1</i> or <i>BRCA2</i>. <b><i>Conclusion:</i></b> Acceptance of recommendation is increasing as clinical consequences augment. Optimization in providing information about hereditary cancer risk and in accessibility of counselling and testing is required to further improve acceptance of recommendation.

scholarly journals EPID-11. THE CONTRIBUTION OF THE rs55705857 G ALLELE TO FAMILIAL CANCER RISK USING THE UTAH POPULATION DATABASE

2016 ◽  
Vol 18 (suppl_6) ◽  
pp. vi57-vi57
Author(s):  
Sarah Hummel ◽  
Wendy Kohlmann ◽  
Thomas Kollmeyer ◽  
Robert Jenkins ◽  
Joshua Sonnen ◽  
...  
Keyword(s):  
Cancer Risk ◽  
Familial Cancer ◽  
Population Database ◽  
Familial Cancer Risk

scholarly journals The contribution of the rs55705857 G allele to familial cancer risk as estimated in the Utah population database

BMC Cancer ◽  
2019 ◽  
Vol 19 (1) ◽  
Author(s):  
Sarah Hummel ◽  
Wendy Kohlmann ◽  
Thomas M. Kollmeyer ◽  
Robert Jenkins ◽  
Joshua Sonnen ◽  
...  
Keyword(s):  
Cancer Risk ◽  
Familial Cancer ◽  
Population Database ◽  
Familial Cancer Risk

scholarly journals Effectiveness of interventions to identify and manage patients with familial cancer risk in primary care: a systematic review

2019 ◽  
Vol 11 (1) ◽  
pp. 73-83
Author(s):  
Siang Ing Lee ◽  
Mitesh Patel ◽  
Brittany Dutton ◽  
Stephen Weng ◽  
Jocelyn Luveta ◽  
...  
Keyword(s):  
Systematic Review ◽  
Primary Care ◽  
Cancer Risk ◽  
Familial Cancer ◽  
Familial Cancer Risk
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