TY - JOUR
T1 - The Population-level Effect of Adjuvant Therapies on Breast Cancer Recurrence
T2 - Application of the Trend-in-Trend Design
AU - Collin, Lindsay J
AU - Waller, Lance A
AU - Cronin-Fenton, Deirdre P
AU - Ahern, Thomas P
AU - Goodman, Michael
AU - McCullough, Lauren E
AU - Kjærsgaard, Anders
AU - Woolpert, Kirsten M
AU - Silliman, Rebecca A
AU - Christiansen, Peer M
AU - Ejlertsen, Bent
AU - Toft Sørensen, Henrik
AU - Lash, Timothy L
N1 - Copyright © 2024 Wolters Kluwer Health, Inc. All rights reserved.
PY - 2024/9/1
Y1 - 2024/9/1
N2 - 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.
AB - 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.
KW - Humans
KW - Breast Neoplasms/drug therapy
KW - Female
KW - Tamoxifen/therapeutic use
KW - Middle Aged
KW - Neoplasm Recurrence, Local/epidemiology
KW - Trastuzumab/therapeutic use
KW - Chemotherapy, Adjuvant
KW - Adult
KW - Receptors, Estrogen
KW - Denmark/epidemiology
KW - Pharmacoepidemiology
KW - Aged
KW - Antineoplastic Agents, Hormonal/therapeutic use
KW - Premenopause
KW - Receptor, ErbB-2
KW - Postmenopause
UR - http://www.scopus.com/inward/record.url?scp=85200828398&partnerID=8YFLogxK
U2 - 10.1097/EDE.0000000000001753
DO - 10.1097/EDE.0000000000001753
M3 - Journal article
C2 - 39109817
SN - 1044-3983
VL - 35
SP - 660
EP - 666
JO - Epidemiology (Cambridge, Mass.)
JF - Epidemiology (Cambridge, Mass.)
IS - 5
ER -