| Literature DB >> 30771221 |
Harindra Jayasekara1,2,3,4, Robert J MacInnis1,2, James A Chamberlain2, Gillian S Dite1, Nicole M Leoce5, James G Dowty1, Adrian Bickerstaffe1, Aung Ko Win1,4,6, Roger L Milne1,2,7, Graham G Giles1,2, Mary Beth Terry5,8, Diana M Eccles9, Melissa C Southey7,10, John L Hopper1.
Abstract
Our aim was to estimate how long-term mortality following breast cancer diagnosis depends on age at diagnosis, tumor estrogen receptor (ER) status, and the time already survived. We used the population-based Australian Breast Cancer Family Study which followed-up 1,196 women enrolled during 1992-1999 when aged <60 years at diagnosis with a first primary invasive breast cancer, over-sampled for younger ages at diagnosis, for whom tumor pathology features and ER status were measured. There were 375 deaths (median follow-up = 15.7; range = 0.8-21.4, years). We estimated the mortality hazard as a function of time since diagnosis using a flexible parametric survival analysis with ER status a time-dependent covariate. For women with ER-negative tumors compared with those with ER-positive tumors, 5-year mortality was initially higher (p < 0.001), similar if they survived to 5 years (p = 0.4), and lower if they survived to 10 years (p = 0.02). The estimated mortality hazard for ER-negative disease peaked at ~3 years post-diagnosis, thereafter declined with time, and at 7 years post-diagnosis became lower than that for ER-positive disease. This pattern was more pronounced for women diagnosed at younger ages. Mortality was also associated with lymph node count (hazard ratio (HR) per 10 nodes = 2.52 [95% CI:2.11-3.01]) and tumor grade (HR per grade = 1.62 [95% CI:1.34-1.96]). The risk of death following a breast cancer diagnosis differs substantially and qualitatively with diagnosis age, ER status and time survived. For women who survive >7 years, those with ER-negative disease will on average live longer, and more so if younger at diagnosis.Entities:
Keywords: breast cancer; cohort study; estrogen receptor; mortality; survival; time-dependent effects
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Year: 2019 PMID: 30771221 PMCID: PMC6697632 DOI: 10.1002/ijc.32214
Source DB: PubMed Journal: Int J Cancer ISSN: 0020-7136 Impact factor: 7.396