TY - JOUR
T1 - Genetic literacy and communication of genetic information in families concerned with hereditary breast and ovarian cancer
T2 - A cross-study comparison in two countries and within a timeframe of more than 10 years
AU - The Cascade Consortium
AU - Pedrazzani, Carla
AU - Ming, Chang
AU - Bürki, Nicole
AU - Caiata-Zufferey, Maria
AU - Chappuis, Pierre O.
AU - Duquette, Debra
AU - Heinimann, Karl
AU - Heinzelmann-Schwarz, Viola
AU - Graffeo-Galbiati, Rossella
AU - Merajver, Sofia D.
AU - Milliron, Kara J.
AU - Monnerat, Christian
AU - Pagani, Olivia
AU - Rabaglio, Manuela
AU - Katapodi, Maria C.
N1 - Funding Information:
The cross-sectional study conducted in 2007 in the U.S. was funded by the Oncology Nursing Foundation, 2007 Major Breast Cancer Research Award. The randomized trial conducted in 2012 in the U.S. was funded by Centers for Disease Control and Prevention (CDC), 5U48DP001901-03 and by the Robert Wood Johnson Foundation (RWJF)—Nurse Faculty Scholars Award (Award # 68039). The ongoing cohort that was initiated in 2017 in Switzerland was funded by the University of Basel, Forschungsfonds 2016; the Swiss Cancer League (KLS-4294-08-2017) and the Swiss Cancer Research Foundation (KFS-5293-02-2021).
Funding Information:
Funding: The cross‐sectional study conducted in 2007 in the U.S. was funded by the Oncology Nurs‐ ing Foundation, 2007 Major Breast Cancer Research Award. The randomized trial conducted in 2012 in the U.S. was funded by Centers for Disease Control and Prevention (CDC), 5U48DP001901‐03 and by the Robert Wood Johnson Foundation (RWJF)—Nurse Faculty Scholars Award (Award # 68039). The ongoing cohort that was initiated in 2017 in Switzerland was funded by the University of Basel, Forschungsfonds 2016; the Swiss Cancer League (KLS‐4294‐08‐2017) and the Swiss Cancer Research Foundation (KFS‐5293‐02‐2021).
Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2021/12/1
Y1 - 2021/12/1
N2 - Examining genetic literacy in families concerned with hereditary breast and ovarian cancer (HBOC) helps understand how genetic information is passed on from individuals who had genetic counseling to their at-risk relatives. This cross-study comparison explored genetic literacy both at the individual and the family level using data collected from three sequential studies conducted in the U.S. and Switzerland over ≥10 years. Participants were primarily females, at-risk or confirmed carriers of HBOC-associated pathogenic variants, who had genetic counselling, and ≥1 of their relatives who did not. Fifteen items assessed genetic literacy. Among 1933 individuals from 518 families, 38.5% had genetic counselling and 61.5% did not. Although genetic literacy was higher among participants who had counselling, some risk factors were poorly understood. At the individual level, genetic literacy was associated with having counselling, ≤5 years ago, higher education, and family history of cancer. At the family level, genetic literacy was associated with having counselling, higher education, and a cancer diagnosis. The findings suggest that specific genetic information should be emphasized during consultations, and that at-risk relatives feel less informed about inherited cancer risk, even if information is shared within families. There is a need to increase access to genetic information among at-risk individuals.
AB - Examining genetic literacy in families concerned with hereditary breast and ovarian cancer (HBOC) helps understand how genetic information is passed on from individuals who had genetic counseling to their at-risk relatives. This cross-study comparison explored genetic literacy both at the individual and the family level using data collected from three sequential studies conducted in the U.S. and Switzerland over ≥10 years. Participants were primarily females, at-risk or confirmed carriers of HBOC-associated pathogenic variants, who had genetic counselling, and ≥1 of their relatives who did not. Fifteen items assessed genetic literacy. Among 1933 individuals from 518 families, 38.5% had genetic counselling and 61.5% did not. Although genetic literacy was higher among participants who had counselling, some risk factors were poorly understood. At the individual level, genetic literacy was associated with having counselling, ≤5 years ago, higher education, and family history of cancer. At the family level, genetic literacy was associated with having counselling, higher education, and a cancer diagnosis. The findings suggest that specific genetic information should be emphasized during consultations, and that at-risk relatives feel less informed about inherited cancer risk, even if information is shared within families. There is a need to increase access to genetic information among at-risk individuals.
KW - Family communication
KW - Genetic affinity
KW - Genetic counselling
KW - Genetic information
KW - Informing at-risk relatives
KW - Knowledge of genetic risk factors
KW - Sensitivity analysis
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U2 - 10.3390/cancers13246254
DO - 10.3390/cancers13246254
M3 - Article
C2 - 34944873
AN - SCOPUS:85121256909
SN - 2072-6694
VL - 13
JO - Cancers
JF - Cancers
IS - 24
M1 - 6254
ER -