TY - JOUR
T1 - Association of endocrine therapy and dementia in women with breast cancer
AU - Thompson, Mikayla R.
AU - Niu, Jiangong
AU - Lei, Xiudong
AU - Nowakowska, Malgorzata
AU - Wehner, Mackenzie R.
AU - Giordano, Sharon H.
AU - Nead, Kevin T.
N1 - Funding Information:
The research was supported, in part, by National Institutes of Health CCSG P30 CA016672. Dr . Nead and Dr . W ehner are Cancer Prevention Research Institute of T exas (CPRIT) Scholars in Cancer Research. Dr . Nead is supported by CPRIT RR190077. Dr . W ehner is supported by CPRIT FP9178. Dr . Giordano is supported by CPRIT RP160674 and Komen SAC150061. The funding organizations had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review , or approval of the manuscript; and decision to submit the manuscript for publication. Dr . Nead had full access to all the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis. Dr . Niu conducted and is responsible for the data analysis.
Publisher Copyright:
© 2021 Thompson et al.
PY - 2021
Y1 - 2021
N2 - Purpose: Prior studies have reported differing results regarding the association between endocrine therapy (ET) in the treatment of breast cancer and dementia risk. However, existing findings may be limited by common sources of bias and confounding. Here we investigate the association of ET utilized in the definitive setting to treat non-metastatic breast cancer with dementia risk accounting for multiple potential sources of bias and confounding. Patients and Methods: We conducted a retrospective study in SEER-Medicare of women aged ≥ 66 years with non-metastatic breast cancer. We examined the risk of all-cause dementia among ET users versus non-ET users using multivariable regression models, accounting for the competing risk of death, and using a start of the follow-up period as 12-months following breast cancer diagnosis for both groups to avoid immortal time bias. Results: Among 25,777 individuals there were 2,869 incident dementia cases. We found a statistically significantly decreased risk of any dementia among ET users in unadjusted and adjusted models that completely attenuated when accounting for the competing risk of death (hazard ratio, 0.98; 95% confidence interval, 0.90–1.07). Conclusion: When accounting for common sources of bias and confounding we did not find evidence to support an association between ET in the definitive treatment of non-metastatic breast cancer and dementia risk. These results suggest that ET may not be associated with dementia risk.
AB - Purpose: Prior studies have reported differing results regarding the association between endocrine therapy (ET) in the treatment of breast cancer and dementia risk. However, existing findings may be limited by common sources of bias and confounding. Here we investigate the association of ET utilized in the definitive setting to treat non-metastatic breast cancer with dementia risk accounting for multiple potential sources of bias and confounding. Patients and Methods: We conducted a retrospective study in SEER-Medicare of women aged ≥ 66 years with non-metastatic breast cancer. We examined the risk of all-cause dementia among ET users versus non-ET users using multivariable regression models, accounting for the competing risk of death, and using a start of the follow-up period as 12-months following breast cancer diagnosis for both groups to avoid immortal time bias. Results: Among 25,777 individuals there were 2,869 incident dementia cases. We found a statistically significantly decreased risk of any dementia among ET users in unadjusted and adjusted models that completely attenuated when accounting for the competing risk of death (hazard ratio, 0.98; 95% confidence interval, 0.90–1.07). Conclusion: When accounting for common sources of bias and confounding we did not find evidence to support an association between ET in the definitive treatment of non-metastatic breast cancer and dementia risk. These results suggest that ET may not be associated with dementia risk.
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U2 - 10.2147/BCTT.S300455
DO - 10.2147/BCTT.S300455
M3 - Article
C2 - 33854369
AN - SCOPUS:85104602641
SN - 1179-1314
VL - 13
SP - 219
EP - 224
JO - Breast Cancer: Targets and Therapy
JF - Breast Cancer: Targets and Therapy
ER -