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

Authors

null

Kathy Pan

Harbor-UCLA Medical Center, Torrance, CA

Kathy Pan , Rowan T. Chlebowski , Michael S. Simon , Roberta Ray , Jennifer Livaudais-Toman , Shannon D. Sullivan , Marcia L. Stefanick , Robert B. Wallace , Meryl LeBoff , Elizabeth C. Bluhm , Electra D. Paskett

Organizations

Harbor-UCLA Medical Center, Torrance, CA, Los Angeles BioMedical Research Institute at Harbor-UCLA Medical Center, Torrance, CA, Karmanos Cancer Inst, Detroit, MI, Fred Hutchinson Cancer Research Center, Seattle, WA, UC San Francisco, San Francisco, CA, MedStar Washington Hospital Center, Washington, DC, Stanford Prevention Research Center, Stanford, CA, University of Iowa College of Public Health, Iowa City, IA, Brigham and Women's Hospital, Boston, MA, The Ohio State University Comprehensive Cancer Center, Columbus, OH

Research Funding

No funding sources reported

Background: While distinct health issues are associated with breast cancer and related therapies, comprehensive assessment of medication use before and after breast cancer diagnosis compared to age-matched, cancer-free controls has not been reported. Methods: From the 93,338 postmenopausal participants in the Women’s Health Initiative trials, medication inventories by pill container review were serially obtained before and > 3 years (mean 5.3 + 2.1 SD) after early stage breast cancer in 1730 cases matched with 1730 controls on age, dates of initial and follow-up medication inventories, body mass index, and smoking. Number of medications and medication classes (excluding tamoxifen and aromatase inhibitors [AI]) in cases and controls were compared. Results: Medication use (n) was comparable at baseline in both groups and significantly increased at follow-up in both cases (4.12 + 2.73 vs 6.47 + 3.29, P< .0001) and controls (3.92 + 2.59 vs 5.94 + 3.37, P < .0001), with clinically marginal but statistically significant additional medication use 0.53 ± 3.93 by breast cancer survivors (P < .0001). More breast cancer survivors used antidepressants (15.3% vs 12.2%, P = .006) and bisphosphonates and/or calcium/vitamin D (62.2% vs 54.8%, P < 0.001). Use of the following classes did not differ: anti-diabetic, cardiovascular, anti-anxiety, and narcotic and non-narcotic analgesics. Medication use at follow-up inventory by adjuvant endocrine therapy are outlined below. Medication use in breast cancer survivors on tamoxifen was lower than controls while those on AIs used more medications. Conclusions: Reflecting age-related co-morbidities, medication use significantly increases over time in both breast cancer survivors and controls. Overall, breast cancer impact on medication use is limited.


Breast Cancer
Cases (n=1730)
Controls
(n=1730)
Selected medication
classes (non-endocrine
treatment) mean ± SD
AllCurrent
Tamoxifen
(n=426)
Current AI
(n=331)
No Current
Endocrine
(n=975)
3.95 ± 2.13
(min=0,
max=11)
4.15 ± 2.13
(min=0,
max=11)
3.40 ± 1.89
(min=0,
max=10),
P=.05*
4.85 ± 2.10
(min=0,
max=10).
P=.002*
4.23 ± 2.14
(min=0,
max=11)

*Adjusted Poisson regression used for test of case-control differences.

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Abstract Details

Meeting

2015 ASCO Annual Meeting

Session Type

Poster Session

Session Title

Breast Cancer—HER2/ER

Track

Breast Cancer

Sub Track

ER+

Citation

J Clin Oncol 33, 2015 (suppl; abstr 553)

DOI

10.1200/jco.2015.33.15_suppl.553

Abstract #

553

Poster Bd #

41

Abstract Disclosures

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