Real‐world treatment patterns of adjuvant endocrine therapy and ovarian suppression in premenopausal HR+/HER2+ breast cancer

Author:

Sukumar Jasmine S.1ORCID,Sardesai Sagar2,Ni Andy3,Williams Nicole2,Johnson Kai2,Quiroga Dionisia2ORCID,Ramaswamy Bhuvana2,Wesolowski Robert2,Cherian Mathew2,Stover Daniel G.2ORCID,Gatti‐Mays Margaret2,Pariser Ashley2,Sudheendra Preeti2,George Mridula A.4,Lustberg Maryam5

Affiliation:

1. Department of Breast Medical Oncology The University of Texas MD Anderson Cancer Center Houston Texas USA

2. Division of Medical Oncology The Ohio State University Comprehensive Cancer Center Columbus Ohio USA

3. The Ohio State University, College of Public Health Columbus Ohio USA

4. Division of Medical Oncology Rutgers Cancer Institute of New Jersey New Brunswick New Jersey USA

5. Yale Cancer Center New Haven Connecticut USA

Abstract

AbstractBackgroundThe optimal adjuvant endocrine therapy (ET) in hormone receptor positive (HR+) and human epidermal growth factor receptor 2 positive (HER2+) premenopausal breast cancer (BC) remains unclear. Moreover, the benefit and clinical indications of ovarian suppression (OS) is poorly elucidated. We described real‐world patterns surrounding choice of ET and clinicopathologic features which predicted treatment with OS in a contemporary cohort of premenopausal women with HR+/HER2+ BC.MethodsThis retrospective analysis included premenopausal patients with nonmetastatic HR+/HER2+ BC from the CancerLinQ Discovery database from January 2010 to May 2020. Women were less than 50 years and received chemotherapy, anti‐HER2 therapy, and ET. They were categorized into 1 of 4 groups based on type of ET prescribed at initiation: aromatase inhibitor (AI) + OS, OS, tamoxifen + OS, or tamoxifen. Multivariable logistic regression assessed associations between clinicopathologic features and OS use.ResultsOut of 360,540 patients with BC, 937 were included. The majority (n = 818, 87%) were prescribed tamoxifen, whereas 4 (0.4%), 50 (5.3%), and 65 (6.9%) received OS, tamoxifen + OS and AI + OS, respectively. No clinicopathologic features predicted OS use apart from age; patients <35 years were more likely to receive OS compared with those ≥35 years (odds ratio 2.33, p < 0.001).ConclusionsThis is the first real‐world study evaluating ET treatment patterns in HR+/HER2+ premenopausal BC. OS use was uncommon and the majority received tamoxifen as the preferred ET regardless of most clinicopathologic risk factors. Additional research is needed to optimize ET decisions in young women with this distinct BC subtype.

Publisher

Wiley

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