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Distinct Reproductive Risk Profiles for Intrinsic-Like Breast Cancer Subtypes: Pooled Analysis of Population-Based Studies.

Audrey Y Jung ,
Thomas U Ahearn ,
Sabine Behrens ,
Pooja Middha ,
Manjeet K Bolla ,
Qin Wang ,
Volker Arndt ,
Kristan J Aronson ,
Annelie Augustinsson ,
Laura E Beane Freeman ,
Heiko Becher ,
Hermann Brenner ,
Federico Canzian ,
Lisa A Carey ,
,
Kamila Czene ,
A Heather Eliassen ,
Mikael Eriksson ,
D Gareth Evans ,
Jonine D Figueroa ,
Lin Fritschi ,
Marike Gabrielson ,
Graham G Giles ,
Pascal Guénel ,
Andreas Hadjisavvas ,
Christopher A Haiman ,
Niclas Håkansson ,
Per Hall ,
Ute Hamann ,
Reiner Hoppe ,
John L Hopper ,
Anthony Howell ,
David J Hunter ,
Anika Hüsing ,
Rudolf Kaaks ,
Veli-Matti Kosma ,
Stella Koutros ,
Peter Kraft ,
James V Lacey ,
Loic Le Marchand ,
Jolanta Lissowska ,
Maria A Loizidou ,
Arto Mannermaa ,
Tabea Maurer ,
Rachel A Murphy ,
Andrew F Olshan ,
Håkan Olsson ,
Alpa V Patel ,
Charles M Perou ,
Gad Rennert ,
Rana Shibli ,
Xiao-Ou Shu ,
Melissa C Southey ,
Jennifer Stone ,
Rulla M Tamimi ,
Lauren R Teras ,
Melissa A Troester ,
Thérèse Truong ,
Celine M Vachon ,
Sophia S Wang ,
Alicja Wolk ,
Anna H Wu ,
Xiaohong R Yang ,
Wei Zheng ,
Alison M Dunning ,
Paul D P Pharoah ,
Douglas F Easton ,
Roger L Milne ,
Nilanjan Chatterjee ,
Marjanka K Schmidt ,
Montserrat García-Closas ,
Jenny Chang-Claude

Abstract

METHODS

Analyses included up to 23 353 cases and 71 072 controls pooled from 31 population-based case-control or cohort studies in the Breast Cancer Association Consortium across 16 countries on 4 continents. Polytomous logistic regression was used to estimate the association between reproductive factors and risk of breast cancer by intrinsic-like subtypes (luminal A-like, luminal B-like, luminal B-HER2-like, HER2-enriched-like, and triple-negative breast cancer) and by invasiveness. All statistical tests were 2-sided.

CONCLUSIONS

This large and comprehensive study demonstrates a distinct reproductive risk factor profile for triple-negative breast cancer compared with other subtypes, with implications for the understanding of disease etiology and risk prediction.

RESULTS

Compared with nulliparous women, parous women had a lower risk of luminal A-like, luminal B-like, luminal B-HER2-like, and HER2-enriched-like disease. This association was apparent only after approximately 10 years since last birth and became stronger with increasing time (odds ratio [OR] = 0.59, 95% confidence interval [CI] = 0.49 to 0.71; and OR = 0.36, 95% CI = 0.28 to 0.46 for multiparous women with luminal A-like tumors 20 to less than 25 years after last birth and 45 to less than 50 years after last birth, respectively). In contrast, parous women had a higher risk of triple-negative breast cancer right after their last birth (for multiparous women: OR = 3.12, 95% CI = 2.02 to 4.83) that was attenuated with time but persisted for decades (OR = 1.03, 95% CI = 0.79 to 1.34, for multiparous women 25 to less than 30 years after last birth). Older age at first birth (Pheterogeneity < .001 for triple-negative compared with luminal A-like breast cancer) and breastfeeding (Pheterogeneity < .001 for triple-negative compared with luminal A-like breast cancer) were associated with lower risk of triple-negative breast cancer but not with other disease subtypes. Younger age at menarche was associated with higher risk of all subtypes; older age at menopause was associated with higher risk of luminal A-like but not triple-negative breast cancer. Associations for in situ tumors were similar to luminal A-like.

BACKGROUND

Reproductive factors have been shown to be differentially associated with risk of estrogen receptor (ER)-positive and ER-negative breast cancer. However, their associations with intrinsic-like subtypes are less clear.

More about this publication

Journal of the National Cancer Institute

Volume 114
Issue nr. 12
Pages 1706-1719
Publication date 08-12-2022

Full text links

Publisher website (DOI) 10.1093/jnci/djac117
Europe PubMed Central 35723569
Pubmed 35723569

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