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Medication use trajectories of postmenopausal breast cancer survivors and matched cancer-free controls
Journal article   Peer reviewed

Medication use trajectories of postmenopausal breast cancer survivors and matched cancer-free controls

Kathy Pan, Rowan T Chlebowski, Michael S Simon, Roberta M Ray, Jennifer Livaudais-Toman, Shannon D Sullivan, Marcia L Stefanick, Robert B Wallace, Meryl LeBoff, Elizabeth Carhart Bluhm, …
Breast cancer research and treatment, Vol.156(3), pp.567-576
04/2016
DOI: 10.1007/s10549-016-3773-4
PMCID: PMC5053395
PMID: 27075917

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Abstract

While adverse medical sequelae are associated with breast cancer therapies, information on breast cancer impact on medication use is limited. Therefore, we compared medication use before and after diagnosis of early stage breast cancer to medication use in matched, cancer-free controls. Of 68,132 Women's Health Initiative participants, 3726 were diagnosed with breast cancer and, after exclusions, in 1731 breast cancer cases, medication use before and >3 years after diagnosis (mean 5.3 ± 2.1 SD) was compared to use in 1731 cancer-free matched controls on similar inventory dates. The medication category number at follow-up inventory was the primary study outcome. Medication category use (n, mean, SD) was comparable at baseline and significantly increased at follow-up in both cases (2.48 ± 1.66 vs. 4.15 ± 2.13, baseline vs follow-up, respectively, P < .0001) and controls (2.44 ± 1.67 vs. 3.95 ± 2.13, respectively, P < .0001), with clinically marginal but statistically significant additional medication category use by cases (0.20 ± 2.40, P < .0001). Tamoxifen users used somewhat more selected medication categories at follow-up assessment (mean 3.40 ± 1.89 vs. 3.21 ± 1.99, respectively, P = 0.05), while aromatase inhibitor users used more medication categories (mean 4.85 ± 2.10 vs. 4.44 ± 1.94, respectively, P = 0.02). No increase in medication category was seen in cases who were not current endocrine therapy users. Breast cancer survivors having only a clinically marginal increase in medication use compared to cancer-free controls. These findings highlight the importance of incorporation of control populations in studies of cancer survivorship.
Comorbidity Aged Aromatase Inhibitors - therapeutic use Breast Neoplasms - drug therapy Female Humans Middle Aged Postmenopause Survivors Tamoxifen - therapeutic use

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