Age-specific breast and ovarian cancer risks associated with germline BRCA1 or BRCA2 pathogenic variants - an Asian study of 572 families

Background Clinical management of Asian BRCA1 and BRCA2 pathogenic variants (PV) carriers remains challenging due to imprecise age-specific breast (BC) and ovarian cancer (OC) risks estimates. We aimed to refine these estimates using six multi-ethnic studies in Asia. Methods Data were collected on 2...

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Main Authors: Ho, Weang-Kee, Hassan, Nur Tiara, Yoon, Sook-Yee, Yang, Xin, Lim, Joanna M. C., Ishak, Nur Diana Binte, Ho, Peh Joo, Wijaya, Eldarina A., Ng, Patsy Pei-Sze, Luccarini, Craig, Allen, Jamie, Tai, Mei-Chee, Chiang, Jianbang, Zhang, Zewen, See, Mee-Hoong, Thong, Meow-Keong, Woo, Yin-Ling, Dunning, Alison M., Hartman, Mikael, Yip, Cheng-Har, Taib, Nur Aishah Mohd, Easton, Douglas F., Li, Jingme, Ngeow, Joanne, Antoniou, Antonis C., Teo, Soo-Hwang
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Published: Elsevier 2024
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Online Access:http://eprints.um.edu.my/45660/
https://doi.org/10.1016/j.lanwpc.2024.101017
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spelling my.um.eprints.456602024-11-07T04:24:10Z http://eprints.um.edu.my/45660/ Age-specific breast and ovarian cancer risks associated with germline BRCA1 or BRCA2 pathogenic variants - an Asian study of 572 families Ho, Weang-Kee Hassan, Nur Tiara Yoon, Sook-Yee Yang, Xin Lim, Joanna M. C. Ishak, Nur Diana Binte Ho, Peh Joo Wijaya, Eldarina A. Ng, Patsy Pei-Sze Luccarini, Craig Allen, Jamie Tai, Mei-Chee Chiang, Jianbang Zhang, Zewen See, Mee-Hoong Thong, Meow-Keong Woo, Yin-Ling Dunning, Alison M. Hartman, Mikael Yip, Cheng-Har Taib, Nur Aishah Mohd Easton, Douglas F. Li, Jingme Ngeow, Joanne Antoniou, Antonis C. Teo, Soo-Hwang R Medicine (General) Background Clinical management of Asian BRCA1 and BRCA2 pathogenic variants (PV) carriers remains challenging due to imprecise age-specific breast (BC) and ovarian cancer (OC) risks estimates. We aimed to refine these estimates using six multi-ethnic studies in Asia. Methods Data were collected on 271 BRCA1 and 301 BRCA2 families from Malaysia and Singapore, ascertained through population/hospital-based case-series (88%) and genetic clinics (12%). Age-specific cancer risks were estimated using a modified segregation analysis method, adjusted for ascertainment. Findings BC and OC relative risks (RRs) varied across age groups for both BRCA1 and BRCA2. The age-specific RR estimates were similar across ethnicities and country of residence. For BRCA1 carriers of Malay, Indian and Chinese ancestry born between 1950 and 1959 in Malaysia, the cumulative risk (95% CI) of BC by age 80 was 40% (36%-44%), 49% (44%-53%) and 55% (51%-60%), respectively. The corresponding estimates for BRCA2 were 29% (26-32%), 36% (33%-40%) and 42% (38%-45%). The corresponding cumulative BC risks for Singapore residents from the same birth cohort, where the underlying population cancer incidences are higher compared to Malaysia, were higher, varying by ancestry group between 57 and 61% for BRCA1, and between 43 and 47% for BRCA2 carriers. The cumulative risk of OC by age 80 was 31% (27-36%) for BRCA1 and 12% (10%-15%) for BRCA2 carriers in Malaysia born between 1950 and 1959; and 42% (34-50%) for BRCA1 and 20% (14-27%) for BRCA2 carriers of the same birth cohort in Singapore. There was evidence of increased BC and OC risks for women from >1960 birth cohorts (p -value = 3.6 x 10-5 for BRCA1 and 0.018 for BRCA2). Interpretation The absolute age -specific cancer risks of Asian carriers vary depending on the underlying populationspecific cancer incidences, and hence should be customised to allow for more accurate cancer risk management. Funding Wellcome Trust grant no: v203477/Z/16/Z]; CRUK (PPRPGM-Nov20\textbackslash100002). Elsevier 2024-03 Article PeerReviewed Ho, Weang-Kee and Hassan, Nur Tiara and Yoon, Sook-Yee and Yang, Xin and Lim, Joanna M. C. and Ishak, Nur Diana Binte and Ho, Peh Joo and Wijaya, Eldarina A. and Ng, Patsy Pei-Sze and Luccarini, Craig and Allen, Jamie and Tai, Mei-Chee and Chiang, Jianbang and Zhang, Zewen and See, Mee-Hoong and Thong, Meow-Keong and Woo, Yin-Ling and Dunning, Alison M. and Hartman, Mikael and Yip, Cheng-Har and Taib, Nur Aishah Mohd and Easton, Douglas F. and Li, Jingme and Ngeow, Joanne and Antoniou, Antonis C. and Teo, Soo-Hwang (2024) Age-specific breast and ovarian cancer risks associated with germline BRCA1 or BRCA2 pathogenic variants - an Asian study of 572 families. Lancet Regional Health-Western Pacific, 44. p. 101017. ISSN 2666-6065, DOI https://doi.org/10.1016/j.lanwpc.2024.101017 <https://doi.org/10.1016/j.lanwpc.2024.101017>. https://doi.org/10.1016/j.lanwpc.2024.101017 10.1016/j.lanwpc.2024.101017
institution Universiti Malaya
building UM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaya
content_source UM Research Repository
url_provider http://eprints.um.edu.my/
topic R Medicine (General)
spellingShingle R Medicine (General)
Ho, Weang-Kee
Hassan, Nur Tiara
Yoon, Sook-Yee
Yang, Xin
Lim, Joanna M. C.
Ishak, Nur Diana Binte
Ho, Peh Joo
Wijaya, Eldarina A.
Ng, Patsy Pei-Sze
Luccarini, Craig
Allen, Jamie
Tai, Mei-Chee
Chiang, Jianbang
Zhang, Zewen
See, Mee-Hoong
Thong, Meow-Keong
Woo, Yin-Ling
Dunning, Alison M.
Hartman, Mikael
Yip, Cheng-Har
Taib, Nur Aishah Mohd
Easton, Douglas F.
Li, Jingme
Ngeow, Joanne
Antoniou, Antonis C.
Teo, Soo-Hwang
Age-specific breast and ovarian cancer risks associated with germline BRCA1 or BRCA2 pathogenic variants - an Asian study of 572 families
description Background Clinical management of Asian BRCA1 and BRCA2 pathogenic variants (PV) carriers remains challenging due to imprecise age-specific breast (BC) and ovarian cancer (OC) risks estimates. We aimed to refine these estimates using six multi-ethnic studies in Asia. Methods Data were collected on 271 BRCA1 and 301 BRCA2 families from Malaysia and Singapore, ascertained through population/hospital-based case-series (88%) and genetic clinics (12%). Age-specific cancer risks were estimated using a modified segregation analysis method, adjusted for ascertainment. Findings BC and OC relative risks (RRs) varied across age groups for both BRCA1 and BRCA2. The age-specific RR estimates were similar across ethnicities and country of residence. For BRCA1 carriers of Malay, Indian and Chinese ancestry born between 1950 and 1959 in Malaysia, the cumulative risk (95% CI) of BC by age 80 was 40% (36%-44%), 49% (44%-53%) and 55% (51%-60%), respectively. The corresponding estimates for BRCA2 were 29% (26-32%), 36% (33%-40%) and 42% (38%-45%). The corresponding cumulative BC risks for Singapore residents from the same birth cohort, where the underlying population cancer incidences are higher compared to Malaysia, were higher, varying by ancestry group between 57 and 61% for BRCA1, and between 43 and 47% for BRCA2 carriers. The cumulative risk of OC by age 80 was 31% (27-36%) for BRCA1 and 12% (10%-15%) for BRCA2 carriers in Malaysia born between 1950 and 1959; and 42% (34-50%) for BRCA1 and 20% (14-27%) for BRCA2 carriers of the same birth cohort in Singapore. There was evidence of increased BC and OC risks for women from >1960 birth cohorts (p -value = 3.6 x 10-5 for BRCA1 and 0.018 for BRCA2). Interpretation The absolute age -specific cancer risks of Asian carriers vary depending on the underlying populationspecific cancer incidences, and hence should be customised to allow for more accurate cancer risk management. Funding Wellcome Trust grant no: v203477/Z/16/Z]; CRUK (PPRPGM-Nov20\textbackslash100002).
format Article
author Ho, Weang-Kee
Hassan, Nur Tiara
Yoon, Sook-Yee
Yang, Xin
Lim, Joanna M. C.
Ishak, Nur Diana Binte
Ho, Peh Joo
Wijaya, Eldarina A.
Ng, Patsy Pei-Sze
Luccarini, Craig
Allen, Jamie
Tai, Mei-Chee
Chiang, Jianbang
Zhang, Zewen
See, Mee-Hoong
Thong, Meow-Keong
Woo, Yin-Ling
Dunning, Alison M.
Hartman, Mikael
Yip, Cheng-Har
Taib, Nur Aishah Mohd
Easton, Douglas F.
Li, Jingme
Ngeow, Joanne
Antoniou, Antonis C.
Teo, Soo-Hwang
author_facet Ho, Weang-Kee
Hassan, Nur Tiara
Yoon, Sook-Yee
Yang, Xin
Lim, Joanna M. C.
Ishak, Nur Diana Binte
Ho, Peh Joo
Wijaya, Eldarina A.
Ng, Patsy Pei-Sze
Luccarini, Craig
Allen, Jamie
Tai, Mei-Chee
Chiang, Jianbang
Zhang, Zewen
See, Mee-Hoong
Thong, Meow-Keong
Woo, Yin-Ling
Dunning, Alison M.
Hartman, Mikael
Yip, Cheng-Har
Taib, Nur Aishah Mohd
Easton, Douglas F.
Li, Jingme
Ngeow, Joanne
Antoniou, Antonis C.
Teo, Soo-Hwang
author_sort Ho, Weang-Kee
title Age-specific breast and ovarian cancer risks associated with germline BRCA1 or BRCA2 pathogenic variants - an Asian study of 572 families
title_short Age-specific breast and ovarian cancer risks associated with germline BRCA1 or BRCA2 pathogenic variants - an Asian study of 572 families
title_full Age-specific breast and ovarian cancer risks associated with germline BRCA1 or BRCA2 pathogenic variants - an Asian study of 572 families
title_fullStr Age-specific breast and ovarian cancer risks associated with germline BRCA1 or BRCA2 pathogenic variants - an Asian study of 572 families
title_full_unstemmed Age-specific breast and ovarian cancer risks associated with germline BRCA1 or BRCA2 pathogenic variants - an Asian study of 572 families
title_sort age-specific breast and ovarian cancer risks associated with germline brca1 or brca2 pathogenic variants - an asian study of 572 families
publisher Elsevier
publishDate 2024
url http://eprints.um.edu.my/45660/
https://doi.org/10.1016/j.lanwpc.2024.101017
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