The Population-level Effect of Adjuvant Therapies on Breast Cancer Recurrence: Application of the Trend-in-Trend Design

Author:

Collin Lindsay J.1ORCID,Waller Lance A.2,Cronin-Fenton Deirdre P.34,Ahern Thomas P.5,Goodman Michael6,McCullough Lauren E.6,Kjærsgaard Anders34,Woolpert Kirsten M.34,Silliman Rebecca A.7,Christiansen Peer M.89,Ejlertsen Bent910,Toft Sørensen Henrik34,Lash Timothy L.6

Affiliation:

1. Department of Population Health Sciences, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT

2. Department of Biostatistics and Bioinformatics, Rollins School of Public Health, Emory University, Atlanta, GA

3. Department of Clinical Epidemiology, University and Aarhus University Hospital, Aarhus, Denmark

4. Department of Clinical Medicine, Aarhus University and Aarhus University Hospital, Aarhus, Denmark

5. Department of Surgery, The Robert Larner, M.D. College of Medicine at The University of Vermont, Burlington, VT

6. Department of Epidemiology, Rollins School of Public Health, Emory University, Atlanta, GA

7. Department of Medicine, Boston University School of Medicine, Boston University, Boston, MA

8. Department of Plastic and Breast Surgery, Aarhus University Hospital, Aarhus, Denmark

9. Danish Breast Cancer Group, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark

10. Rigshospitalet, Copenhagen, Denmark

Abstract

Purpose: Breast cancer has an average 10-year relative survival reaching 84%. This favorable survival is due, in part, to the introduction of biomarker-guided therapies. We estimated the population-level effect of the introduction of two adjuvant therapies—tamoxifen and trastuzumab—on recurrence using the trend-in-trend pharmacoepidemiologic study design. Methods: We ascertained data on women diagnosed with nonmetastatic breast cancer who were registered in the Danish Breast Cancer Group clinical database. We used the trend-in-trend design to estimate the population-level effect of the introduction of (1) tamoxifen for postmenopausal women with estrogen receptor (ER)-positive breast cancer in 1982, (2) tamoxifen for premenopausal women diagnosed with ER-positive breast cancer in 1999, and (3) trastuzumab for women <60 years diagnosed with human epidermal growth factor receptor 2-positive breast cancer in 2007. Results: For the population-level effect of the introduction of tamoxifen among premenopausal women diagnosed with ER-positive breast cancer in 1999, the risk of recurrence decreased by nearly one-half (OR = 0.52), consistent with evidence from clinical trials; however, the estimate was imprecise (95% confidence interval [CI] = 0.25, 1.85). We observed an imprecise association between tamoxifen use and recurrence from the time it was introduced in 1982 (OR = 1.24 95% CI = 0.46, 5.11), inconsistent with prior knowledge from clinical trials. For the introduction of trastuzumab in 2007, the estimate was also consistent with trial evidence, though imprecise (OR = 0.51; 95% CI = 0.21, 22.4). Conclusions: We demonstrated how novel pharmacoepidemiologic analytic designs can be used to evaluate the routine clinical care and effectiveness of therapeutic advancements in a population-based setting while considering some limitations of the approach.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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